Table of Contents
Page created on April 29, 2020. Last updated on July 14, 2020 at 16:22
Summary of cancer treatments
- Treatment of head and neck cancers
- Cancer of oral cavity -> surgery, adjuvant RT or RCT if high-risk features
- Cancer of pharynx
- Nasopharynx -> RCT
- Oropharynx -> RCT/surgery
- Hypopharynx -> surgery
- Cancer of larynx
- Early cancer -> RT/surgery
- Locally advanced cancer -> RCT/total laryngectomy
- Advanced cancer -> total laryngectomy + adjuvant RT
- Stage III and IV head and neck cancers -> RCT/radiobiotherapy
- Treatment of NSCLC
- Stage I – IIIa -> surgery ± adjuvant CT
- Stage IIIb -> RCT
- Stage IIIc – IV
- Squamous cell carcinoma -> polychemotherapy ± immunotherapy
- Adenocarcinoma -> targeted therapy against EGFR, ALK, ROS
- Treatment of SCLC
- Limited disease -> RCT + prophylactic cranial irradiation if remission is achieved
- Extensive disease -> CT + prophylactic cranial irradiation in most cases
- Treatment of breast cancer
- Early breast cancer
- Without BRCA mutation -> breast-conserving surgery + adjuvant RT
- With BRCA mutation -> Mastectomy + prophylactic contralateral mastectomy + prophylactic bilateral salpingo-oopherectomy
- For locally advanced breast cancer -> neoadjuvant systemic therapy + surgery + adjuvant systemic therapy
- For metastatic breast cancer -> neoadjuvant systemic therapy + surgery and/or RT
- With BRCA mutation -> PARP inhibitors
- Early breast cancer
- Treatment of oesophageal cancer
- Localized disease -> neoadjuvant CT/RCT + surgery + adjuvant CT
- Advanced disease -> RCT/targeted/immunotherapy
- Treatment of gastric cancer
- Localized disease -> neoadjuvant CT/RCT + surgery + adjuvant CT/RCT
- Advanced disease -> neoadjuvant CT + surgery + adjuvant CT ± targeted/immunotherapy
- Treatment of pancreatic cancer
- Resectable disease -> surgery + adjuvant CT/RCT
- Non-resectable disease -> CT ± palliative surgery
- Treatment of HCC
- Very early or early stage -> Surgery
- Early stage -> Liver transplant
- Intermediate stage -> TACE
- Advanced stage -> Sorafenib
- Terminal stage -> Palliative
- Treatment of CRC
- Stage I -> Surgery
- Stage II, III -> Surgery + adjuvant CT
- Stage IV -> Palliative
- Treatment of non-melanoma skin cc (BCC, SCC) -> surgery
- Treatment of melanoma
- Localized disease -> surgery
- Regional and metastatic disease -> surgery + adjuvant targeted/immuno
- Treatment of CNS tumours
- Low-grade glioma -> surgery
- High-grade glioma -> surgery + RCT (temozolomide)
- Multiple brain mets -> whole brain radiotherapy
- Primary CNS lymphoma -> CT (methotrexate)
- Treatment of ovarian cancer
- Stage I, II -> surgery + adjuvant CT
- Stage III, IV -> cytoreduction + adjuvant CT
- Treatment of cervical cancer
- Early cervical disease -> surgery/RT ± adjuvant RCT
- Locally advanced disease -> RCT
- Metastatic disease -> Palliative
- Treatment of endometrial cancer
- Stage I, II -> Surgery + adjuvant RT
- Stage III, IV -> Cytoreduction + adjuvant CT/RT/hormonal
- Treatment of prostate cancer
- Low and intermediate risk localized disease -> Observation/surgery/RT
- High-risk localized and locally advanced disease -> [ADT + ERBT] or surgery
- Hormone-naive metastatic disease -> ADT + antiandrogens
- Castration-resistant metastatic disease -> ADT + antiandrogens + CT/immunotherapy
- Treatment of bladder cancer
- Non-muscle-invasive disease -> TUR-B + intravesical BCG or chemo
- Muscle-invasive disease -> surgery or [TUR-B + RCT]
- Metastatic disease -> palliative
- Treatment of RCC
- Localized disease -> surgery
- Metastatic disease -> targeted/immunotherapy
- Treatment of testicular cancer
- Localized disease -> observation or [orchidectomy + adjuvant CT]
- Locally advanced disease -> orchidectomy + adjuvant RT/CT/RPLND
- Metastatic disease -> orchidectomy + adjuvant CT
Introduction to oncology
- https://www.cancer.org/ is a surprisingly good source for information on the specific malignancies. They explain specific procedures, staging, diagnosis and treatment of all cancers. If there’s something which you don’t understand, I recommend you check there
- Epidemiology
- Most frequent cancers (USA)
- (Except skin cancer, which is the most common)
- Prostate/breast
- Lung and bronchus
- Colorectal
- Cancers causing the most deaths (USA)
- Lung and bronchus
- Prostate/breast
- Colorectal
- Most frequent cancers (USA)
- The clinical courses of cancer patients
- The absolute cure rate is 60%
- 30% survive several years
- 10% experience no real effect of treatment
- CAUTION – cancer’s seven warning signs
- Change in bowel or bladder habits
- A sore that does not heal
- Unusual bleeding or discharge
- Thickening of lump in breast or elsewhere
- Indigestion or difficulty in swallowing
- Obvious change in wart or mole
- Nagging cough or hoarseness
- Grading
- Grading is based on how differentiated the tumor is on histology, compared to healthy tissue
- From G1 (well differentiated) to G4 (very poorly differentiated)
- Special grading systems
- Gleason score – for prostate cancer
- Grading also takes into account:
- The degree of vessel penetration
- Presence of hormonal receptors or growth factor receptors
- Presence of certain gene mutations
- Staging
- TNM staging system is often used
- Brain tumours and haematological malignancies use other systems
- Clinical staging (cTNM) – staging based on the clinical information (obtained before surgery)
- Including physical examination, blood tests, imaging, biopsy, endoscopy, etc.
- Histopathological examination of biopsy is performed for most cancers
- Pathological staging (pTNM) – staging based on the clinical information + information from the pathologist after surgical resection
- Some cancers are not treated surgically, so there will be no pTNM stage, only cTNM stage
- Many tumours are examined histopathologically twice – once of the biopsy taken before surgery, and once of the tumour which was removed during surgery
- Treatment-associated staging (yTNM) – staging after chemotherapy and/or radiation therapy
- Generally:
- Stages I and II are referred to as “early” or “non-invasive” disease
- Stage III is referred to as “locally” or “regionally” “advanced” or “invasive” disease
- Stage IV is referred to as “advanced” or “metastatic” disease
- TNM staging system is often used
- Prognostic factors
- Those factors which determine the patient’s prognosis
- Most important factors
- Grading
- Staging
- Performance status
- Different performance status scales exist
- Eastern Cooperative Oncology Group performance status (ECOG PS)
- Grade 0 – Fully active, no restriction on daily activity
- Grade 4 – Completely disabled, not capable of self-care, totally confined to bed or chair
- Grade 5 – dead
- Karnofsky performance scale (KPS)
- 100 – normal
- 0 – dead
- Other factors
- Age
- The excess of weight loss
- The localization of the disease
- Predictive factors
- Those factors which are associated with response or lack of response to a particular therapy
- For example, the presence of oestrogen receptors in breast cancer is a predictive factor, as it predicts the patient’s response to antioestrogens
- Many predictive factors are also prognostic factors
- Those factors which are associated with response or lack of response to a particular therapy
- Oncological teams
- Cancers patients are treated by oncological teams rather than individual oncologists
- This:
- Optimizes treatments
- Allows learning from each other
- Allows teamwork across multiple modalities (pathology, radiology, etc.)
- Allows responsibility to be shared
- Allows members of the team to support each other
- Includes
- Oncologists
- Pathologists
- Radiologists
- Nurses
- Etc.
- Treatment
- Cancer treatment doesn’t begin until the staging is complete, unless
- The cancer is causing urgent, life-threatening complications
- Complete staging is impossible or too dangerous (certain brain tumours)
- Important factors in treatment decision
- Performance status
- Renal function
- Liver function
- Bone marrow function
- Types of therapy
- Curative therapy – therapy with the intent of curing the cancer
- Palliative therapy – therapy with the intent of relieving symptoms and improving quality of life
- Neoadjuvant therapy – chemo and/or radiation before surgery
- Neoadjuvant therapy can reduce the tumour size, making surgery more likely to be curative
- Adjuvant therapy – chemo and/or radiation after surgery
- Modalities
- Surgery – in 60% of cases
- Radiotherapy – in 30% of cases
- Medical therapy – in 10% of cases
- Modalities are generally combined
- Radiochemotherapy refers to simultaneous use of radio and chemo, as opposed to radio first and then chemo after
- Treatment response
- Complete response/regression (CR) – no evidence of tumour after a certain amount of time
- Partial response/regression (PR) – decrease in tumour volume
- Stable disease (SD) – minimal decrease or increase in tumour volume
- Progressive disease (PD) – increase in tumour volume
- Cancer treatment doesn’t begin until the staging is complete, unless
1. The basic principles of tumor biology
- Etiological factors contributing to cancer development
- Environmental exposure
- Asbestos -> mesothelioma, RCC
- Formaldehyde -> nose and nasopharyngeal cc
- Radiation
- Those with childhood leukaemia often develop solid tumours 10 – 20 years after the radiotherapy
- Lifestyle problems
- Smoking -> lung cancer, head and neck cancer
- Alcohol -> head and neck cancer, oesophageal cancer
- Alimentary factors
- Obesity, diabetes -> CRC
- Hygienic problems
- -> cancer of glans penis
- Infections
- HPV -> cervical cc
- EBV -> nasopharyngeal carcinoma
- Aflatoxin -> HCC
- Hormonal effects
- Oestrogen -> breast cc, endometrial cc
- Testosterone -> prostate cc
- Genetic background
- BCL/ABL => CML
- APC => CRC
- Environmental exposure
- Biological factors contributing to cancer development
- Trouble in communication between cells
- Absence of contact inhibition
- Uncontrolled growth and cell dividing
- Omitting the integrity of neighbouring cells, tissues and organs
- Neo-vascularization and aberrant blood vessels
- The possibility of penetrating blood vessels
- Disturbing the metabolic activity of the organ
- Evolving paraneoplastic symptoms
2. Principles of surgical oncology
- Debulking and cytoreduction
- Debulking or cytoreduction = surgically removing as much of a tumour as possible, in cases where the whole tumour cannot be removed
- Debulking can be performed palliatively, to increase survival, or with curative intent, by increasing the penetration of adjuvant radiation and/or chemo into the tumour
- Performed in ovarian cc, endometrial cc, etc.
- En-bloc resection
- The entire tumour and a continous layer of healthy tissue around it is removed together
- Surgical margin
- During surgery, the margin of the removed tissue is marked with ink
- While the surgeons wait the pathologist will make frozen slides of the removed tissue and examine it histologically
- By using the ink as a reference, the pathologist can determine whether the surgery removed all of the tumour or not
- If the surgical margin is clear/negative/clean, there are no tumour cells at the margin, so further treatment is usually not needed
- If the surgical margin is positive, more surgery or other adjuvant treatment is needed to ensure that no tumour cells remain
- R0 resection – complete resection of the tumour
- No macroscopic evidence of tumour, with negative margins
- R1 resection – microscopic remnants of tumour remain
- No macroscopic evidence of tumour, but positive margins
- R2 resection – macroscopic remnants of tumour remain
- Preoperative (neoadjuvant) and postoperative (adjuvant) therapy
- For some cancers clinical studies have established that neoadjuvant and/or adjuvant therapy is beneficial
- In some cases, postoperative therapy is only indicated if certain features of the tumour are discovered during surgery (during pathological staging), like
- Incomplete (R1, R2) surgical resection
- Spread to lymph nodes
- Certain mutations
- Very deep invasion
- Etc.
- These are features which are associated with high risk of recurrence or poor prognosis
- Postoperative therapy can be chemo, radio, radiochemotherapy, etc.
3. Radiation physics
- Types of radiation used
- Natural radiation (due to radioactive decay)
- Alpha radiation (two protons and two neutrons)
- Beta radiation (high-energy electrons)
- Electrons (beta radiation) has low penetration power, so beta radiation is only suitable for treating tumours near the skin surface
- Gamma radiation (high-energy photons)
- Photon radiation (gamma and X-ray radiation) has high penetration power, so it is suitable for treating deep tumours
- Artificial radiation
- X-rays (gamma radiation which is artificially made)
- Heavy ion radiation
- Heavy ions, like carbon ions, are accelerated to high speeds
- Proton radiation (alpha radiation) and heavy-ion radiation don’t penetrate tissues deeper than a certain point
- This makes these types of radiation suitable for treating tumours where radiation-sensitive tissue is very close, for example inside the skull
- They’re also suitable for treating tumours close to the skin
- This effect is due to the so-called “Bragg peak” on the percentage depth dose distribution
- Natural radiation (due to radioactive decay)
- Particle therapy
- Accelerated protons or heavy ions are sent into the tumour
- Very expensive
- Compton-scattering is the most important radiation effect on tissues in radiotherapy
- The photoelectric effect, pair production and coherent scattering are less important
- The inverse square law
- The law states that the intensity of radiation decreases in an inverse square ratio with the distance from the source of the radiation
- For example
- If the distance from the source is doubled, the radiation intensity is reduced to one fourth
- If the distance from the source is increased three-fold, the radiation intensity is reduced to one ninth
- The inverse square law is important in treatment planning in brachytherapy
- Percentage depth dose (PDD)
- The PDD is the percentage of the maximum dose which is deposited in tissue (or something, it’s confusing)
- PDD is important in treatment planning in teletherapy
- Squamous cell cancers are generally very radiosensitive
- Adenocarcinomas on the other hand, are not
- Radiation biology
- Radiation induces double-stranded breaks in DNA
- The cell is most sensitive to radiation in the M and G2 phases of the cell cycle
- The oxygen effect
- According to the oxygen effect, normoxic tissues and cells are more radiosenstive than hypoxic ones
- The oxygen effect occurs because oxygen “stabilizes” or “makes permanent” the DNA damage produced by reactive oxygen species
- In hypoxic tissues, the DNA damage is not made permanent and can therefore be repaired by the cell
4. The equipment used in radiation oncology
- Types of radiotherapy
- External beam radiation therapy (EBRT)/teletherapy
- The radiation source is outside the patient
- The source can be rotated around the patient, allowing the radiation beam to target the tumour from a variety of directions
- Types
- Conventional external beam therapy
- Three-dimensional conformal radiotherapy (3DCRT)
- Intensity modulated radiation therapy (IMRT)
- Stereotactic radiosurgery/radiotherapy
- A multileaf collimator (MLC) is used to shape the radiation beam
- Especially used in IMRT and 3DCRT
- Internal radiation therapy/brachytherapy
- The radiation source is inside or very close to the patient, as close to the tumour as possible, or even inside the tumour
- Can be temporary or permanent
- Temporary brachytherapy – the radiation source is placed and then removed after some time
- Most common
- Permanent brachytherapy – a small radiation source is permanently placed into the patient
- Also called “seed implantation”
- The radioactive “seed” loses its radioactivity after some months, but won’t be removed
- Temporary brachytherapy – the radiation source is placed and then removed after some time
- Can be high dose-rate (HDR), low dose-rate (LDR) or pulsed dose-rate (PDR)
- HDR reduces the treatment time, and is most commonly used
- HDR = dose rate of more than 12 Gy per hour
- Treatment typically lasts a few minutes
- LDR = dose rate of less than 2 Gy per hour
- Treatment typically lasts 24 hours
- PDR = short pulses of radiation are given
- Treatment typically lasts 24 hours
- Types
- Intracavital brachytherapy
- Into the cervix, bronchi, etc.
- Interstitial brachytherapy
- Into the breast, prostate, etc.
- Intracavital brachytherapy
- Systematic radiation therapy
- An isotope is injected into the patient, by itself or attached to a specific molecule
- The isotope will travel to the tumour and irradiate it from inside
- The isotope often gives off alpha or beta-waves, as these waves don’t travel far in the body
- Alpha waves only travel 100 µm
- Examples
- Radioactive iodine given for thyroid cancer
- Radium-223 given for bone metastases
- External beam radiation therapy (EBRT)/teletherapy
- Equipment used in brachytherapy
- Afterloading
- The technique where a machine (an afterloader) is used to deliver the radiation source into the patient during brachytherapy
- This eliminates the need for a person to deliver the radiation source, eliminating radiation exposure for that person
- Manual delivery of brachytherapy is seldom used for this reason
- Often used with HDR, sometimes called HDR Afterloading
- 192Iridium is often used as radiation source
- Afterloading
- Equipment used in teletherapy
- Cobalt unit
- Older type of teletherapy
- The external beam is generated using 60Cobalt
- Linear accelerator (LINAC)
- More modern than cobalt unit
- Most commonly used device for external beam radiation therapy
- The external beam is generated using linear acceleration
- A multileaf collimator allows precise modification of the radiation field
- Used for stereotactic surgery, intensity modulated radiotherapy, particle therapy etc.
- Gamma knife
- Used for stereotactic radiosurgery in the brain
- Tomotherapy
- CyberKnife
- Cobalt unit
5. Treatment planning, radiation protection
- Treatment planning
- Imaging is used to form a virtual model of the patient, including the tumour
- Native CT is almost always used, because the physical interactions between the radiation and the tissue is the same in native CT as in radiotherapy
- This means that a native CT contains the dose-absorbing properties of the tissues of the patient
- By using image registration and image fusion, multiple imaging modelities may be combined, if needed
- Image registration refers to “matching” multiple imaging modalities by mapping the coordinates of anatomical structures on the different modalities, so that they “match” on top of each other
- Image fusion refers to displaying multiple modalities on top of each other after image registration
- MRI provides good differentiation between different soft tissues
- PET provides good information of functionality and metastases
- Ultrasound cannot be used for treatment planning
- Native CT is almost always used, because the physical interactions between the radiation and the tissue is the same in native CT as in radiotherapy
- Computer systems allow for simulation and calculation of how different radiotherapy approaches would deliver radiation to the tumour and the surrounding tissues
- Modern techniques allow for even more precise radiation planning
- Intensity-modulated radiation therapy (IMRT)
- 3D conformal radiation therapy (3DCRT)
- Intensity-modulated arc therapy (IMAT)
- Image-guided radiation therapy (IGRT)
- Volumes in radiotheapy planning
- Gross tumour volume (GTV) = the volume of the macroscopic tumour
- Clinical target volume (CTV) = the GTV + microscopic, un-imageable tumour spread
- Planning target volume (PTV) = the CTV + uncertainties in planning or delivery
- Imaging is used to form a virtual model of the patient, including the tumour
- Fractionation of radiation therapy
- Most cancers respond based on the total (cumulative) amount of radiation, not the size of the individual doses
- However, side effects are mostly related to the sizes of the individual doses
- As such, the sizes of the doses can be increased or decreased
- Hypofractionated radiation therapy
- When the total dose of radiation is divided into larger but fewer doses
- Used for cancers which are sensitive to large individual radiation doses
- Treatment course is completed quicker
- Often used in breast cancer and prostate cancer
- Hyperfractionated radiation therapy
- When the total dose of radiation is divided into smaller but more doses, often given more than once a day
- May produce fewer side effects
- Used for cancers with high turnover, like SCLC
- Most cancers respond based on the total (cumulative) amount of radiation, not the size of the individual doses
6. Basic concepts of chemotherapy
- Polychemotherapy = simultaneous use of multiple chemo drugs
- The term is not consistently used, even by me
- Recently, we have moved from preferring to use multiple chemo drugs, so the term is kind of reduntant
- Mode of actions
- Induce DNA damage
- Inhibit DNA repair mechanisms
- Inhibit metabolism
- For example nucleotide synthesis
- Inhibit mitosis
- Inhibit neo-vascularization
- Commonly used drugs
- Platinum-based drugs
- Cisplatin
- Very nephrotoxic – renal function must be measured before use
- Carboplatin
- Less nephrotoxic – sometimes used as an alternative to cisplatin in case of poor kidney function
- Cisplatin
- 5-FU
- Taxanes
- Paclitaxel
- Docetaxel
- Platinum-based drugs
- Commonly used regimens
- FLOT
- 5-FU
- Leucovorin
- Oxaliplatin
- DoceTaxel
- FOLFOX
- FOLinic acid (leucovorin)
- 5-FU
- Oxaliplatin
- FOLFIRI
- FOLinic acid
- 5-FU
- IRInotecan
- ECX
- Epirubicin
- Cisplatin
- Capecitabine
- Gem/cis
- Gemcitabine + cisplatin
- XELOX
- Capecitabine + oxaliplatin
- FLOT
7. Basic concepts of hormone therapy
8. Biological therapy, targeted therapy and immunotherapy
- Targeted therapy
- Targeted therapy refers to using drugs which are not cytotoxic but rather specifically target certain molecules
- Targeted therapy often prolongs survival, sometimes for years, and the patient remains on the targeted therapy during this time
- Biological therapy
- = refers to biological drugs, most commonly monoclonal antibodies
- Bevacizumab – anti-VEGF
- Inhibits vascular proliferation and therefore neovascularization
- Cetuximab – anti-EGFR
- Small molecules
- = refers to small molecule drugs, which enter the cells and inhibit certain intracellular proteins
- Gefitinib, erlotinib – EGFR inhibitors
- Alectinib – ALK inhibitor
- Vemurafenib – BRAF inhibitor
- Only works on a certain type of BRAF mutation in melanoma
- Actually stimulates wildtype BRAF
- Sorafenib – Multi protein kinase inhibitor
- Inhibits VEGFR, PDGFR, RAF, etc.
- Common side effects
- Anti-EGFR and EGFR inhibitors
- Acneiform dermatitis
- Anti-BRAF and BRAF inhibitors
- Photosensitivity
- Squamous cell carcinoma
- Sorafenib
- Alopecia
- Hand-foot syndrome
- Anti-EGFR and EGFR inhibitors
- Immunotherapy
- Immune checkpoint inhibitors
- Most commonly used immunotherapy
- These drugs are monoclonal antibodies and therefore also technically biological drugs
- These drugs inhibit the mechanism by which cancer cells inhibit the immune system
- Anti-PD-1 – nivolumab, pembrolizumab
- Anti-CTLA-4 – ipilimumab
- Vaccines
- Cytokines
- Immune checkpoint inhibitors
9. Cancer pain management
- Pain -> opioids
- Nausea -> ondansetron
- Diarrhoea -> loperamide
- Phlebitis -> local anti-inflammatory cream
10. Psycho-oncology
11. Oncologic emergencies
- In case of oncological emergencies oncotherapy can be initiated without knowing the histology of the cancer
- Increased intracranial pressure
- Due to brain metastases or primary brain tumor
- Urgent MRI should be made
- ASAP treatment includes dexamethasone, forced diuresis (fluid + loop diuretics) and mannitol to reduce oedema
- Then treat tumor
- Spinal cord compression
- Due to enlarging vertebral metastasis or pathologic vertebral fracture due to metastasis
- Often from breast, lung, prostate, etc.
- Most often involves thoracic spine
- X-ray will show blastic or lytic lesions
- MRi will show localization of spinal cord compression
- ASAP treatment includes dexamethasone and spinal decompression surgery
- Then treat tumor
- Superior vena cava syndrome
- Can be due to lung cancer, lymphoma etc, but also due to non-cancer conditions (see surgery 1)
- X-ray will show mediastinal widening
- CT with contrast will give more detailed picture
- Hyperfractionated radiation therapy given to provide rapid tumor reduction and symptom relief
- Malignant pleural effusion
- Exudate, not transudate
- Due to tumor cell implants on pleura
- Due to metastatic breast, lung or lymphoma
- Chest x-ray shows effusion
- Thoracentesis shows exudate, also drains fluid
- Chest tube can be inserted to continually drain fluid
- Pleurodesis – procedure where the visceral and parietal pleurae are adhered together to prevent fluid accumulation
- A sclerosing agent like doxycycline, bleomycin or talc is added to the pleural cavity
- These agents cause the pleurae to adhere to each other
- Airway obstruction
- Ileus
- Hypercalcaemia of malignancy
- In breast, lung, or multiple myeloma
- Due to osteolytic metastases, or due to PTH-related peptide secretion
- Symptoms include fatigue, vomiting, altered mental status
- Treatment involves hydration and furosemide + bisphosphonates
- Hyponatraemia
- Due to syndrome of inappropriate ADH, due to SCLC or other neuroendocrine tumor
- ASAP slow infusion of hypertonic saline
- Tumor lysis syndrome
- Due to chemo of chemosensitive, high cell-turnover tumours, especially leukaemias, lymphomas
- Massive cell death release causes hyperkalaemia, hyperuricaemia, hyperphosphataemia, secondary hypocalcaemia
- Prevention is essential, by hydrating patients, possibly giving allopurinol
- Manifest tumor lysis syndrome may require dialysis
- Febrile neutropaenia
- Defined as a single measurement of > 38,3°C oral or a sustained temperature of 38,0°C for 1 hour + neutropaenia (< 500/µL)
- Take two sets of blood culture ASAP, then immediately start empiric broad-spectrum AB therapy
- Aminoglycoside + antipseudomonal beta-lactam
- Disseminated intravascular coagulation
- Due to acute promyelocytic leukaemia (APML)
- Signs of haemorrhage and thrombosis
- All-trans retinoic acid treats APML
- Replacement of platelets and coagulation factors may be necessary
- Hyperviscosity syndrome
- Due to myeloproliferative disease or ALL
- Hyperviscous blood causes symptoms of impaired microcirculation
- Treatment includes phlebotomy
12. Palliative care
Specific malignancies template
- The next topics about specific malignancies will follow this template
- Epidemiology
- Etiology
- Causes, risk factors
- Pathology
- Relevant pathological aspects
- Clinical features
- Signs and symptoms
- Stages
- The clinical and pathological stages. Often based on TNM
- Sometimes the stages are classified like this
- Early stage/localized disease
- The tumour is localized to the primary organ
- Locally/regionally advanced disease
- The tumour has spread locally or to local lymph nodes
- Metastatic/disseminated disease
- The tumour has spread distally (M1)
- Risk groups
- Factors which determine the risk of metastases and poor outcomes
- Often, these include stage, grade, certain lab markers, certain histological features, etc.
- The treatment is often based on the risk group
- Cancers are often divided into low, intermediate and high-risk groups depending on the presence of these factors
- Age and performance status are important factors for all cancers
- Diagnosis
- The process of establishing the diagnosis of cancer
- Work-up after diagnosis
- As soon as the diagnosis is established the staging work-up must begin for the clinical staging of the cancer
- Often includes imaging modalities to evaluate spread and lymph node metastases
- Can also include tests for biomarkers, biopsy of lymph nodes, etc.
- NB! It’s common to do MRI of the brain if metastases are present on imaging
- NB! It’s common to do bone scans if skeletal symptoms are present
- Treatment
- Surgery
- Explains the surgical modalities used, etc.
- Systemic therapy
- Chemotherapy
- Targeted therapy
- Hormonal therapy
- Immunotherapy
- Radiotherapy
- Treatment according to stage:
- Early stage/localized disease
- Locally/regionally advanced disease
- Metastatic/disseminated disease
- Surgery
13. Tumors of head and neck
- Tumours of the head and neck include
- Eye and orbital tumours
- Oral cavity tumours
- Pharyngeal tumours
- Nasopharynx
- Oropharynx
- Hypopharynx
- Laryngeal tumours
- Supraglottic
- Glottic
- Subglottic
- Tumours of the nasal cavity and paranasal sinuses
- Tumours of the salivary gland
- Tumours of the thyroid gland
- Epidemiology
- Head and neck cancer is the 6th most common cancer worldwide
- Etiology
- Smoking
- Alcohol
- Poor oral hygiene
- EBV – for nasopharyngeal carcinoma
- HPV – for oropharyngeal and laryngeal cancer
- Pathology
- 80% are squamous cell
- 20% are adenocarcinoma, lymphoma, sarcoma, etc.
- Precancerous lesions
- Leukoplakia
- Erythroplakia
- Lichen planus
- Metastasizes most often to lung
- Clinical features
- Ulceration of mucosa
- Exophytic growth of mucosa
- Neck mass
- Sore throat
- Hoarseness
- Pain radiating into the ear
- Due to cranial nerve affection
- Dysphagia
- Diagnosis
- FNAB or direct excision biopsy
- Work-up after diagnosis
- CT with contrast or MRI of head and neck
- Laryngoscopy
- Neck US
- PET scan
- Treatment
- Majority of cases are treated with multiple modalities
- Surgery
- Only used if R0 resection with acceptable functional results is expected
- This means that surgery is not performed unless the surgeon believes that he can completely resect the tumour
- If early stage cancer -> transoral surgery (TORS)
- If cancer has spread to lymph nodes, neck dissection must be performed
- Modified radical neck dissection
- Selective neck dissection
- Surgery, especially of pharynx and larynx, impairs quality of life, which must be taken into account when deciding treatment modality
- Only used if R0 resection with acceptable functional results is expected
- Radiotherapy
- External beam radiotherapy or brachytherapy
- Can be given with curative or palliative intention
- Can be given postoperatively or primarily
- Primary radiotherapy alone is usually sufficient in
- Cancer of the lip
- Cancer of the nose
- Cancer of the floor of the mouth (brachytherapy)
- Cutaneous lymphoma
- Chemotherapy
- Cisplatin
- Taxanes
- 5-FU
- Biological and immunotherapy
- Cetuximab (anti-EGFR)
- Nivolumab (anti-PD-1)
- Pembrolizumab (anti-PD-1)
- Cancer of oral cavity
- Surgery
- Postoperative radiotherapy or radiochemotherapy is indicated if high-risk features are present
- R1 or R2 resection
- T3 or T4 tumours
- Lymph node spread
- Etc.
- Before radiotherapy of the oral cavity, dental care is essential
- Bad teeth etc. can act as a source of inflammation after radiotherapy
- Cancer of pharynx
- Nasopharynx is the most radiosensitive, hypopharynx is the least radiosensitive
- Nasopharyngeal cancer – radiochemotherapy
- Oropharyngeal cancer – radiochemotherapy is preferred, surgery is option
- Hypopharyngeal cancer – surgery is preferred, radiochemotherapy is option
- Cancer of larynx
- Early cancer – radio or surgery alone
- Locally advanced cancer – radiochemotherapy or total laryngectomy
- Advanced cancer – total laryngectomy with adjuvant radiotherapy
- Stage III and IV
- Radiochemotherapy or radiobiotherapy
- With cisplatin or cetuximab, respectively
14. Lung cancer
- Epidemiology
- Cancer with the highest mortality rate worldwide
- Etiology
- Smoking
- 80% of lung cancer deaths are due to tobacco use
- Air pollution
- Asbestos
- Smoking
- Clinical features
- Cough
- Haemoptysis
- Dyspnoea
- Chest pain
- Extrapulmonary symptoms
- Superior vena cava syndrome
- Weight loss
- etc.
- Diagnosis
- If lesions suspicious of tumor is found, biopsy must be taken
- Acquiring tissue specimens is better than acquiring cytologic specimens
- As only tissue specimens yield enough material for immunohistochemistry and genetical testing
- This is important for prognosis and treatment
- However, cytologic specimen is usually sufficient to determine the histological subtype and to confirm the cancer diagnosis
- Procedures which yield tissue specimens
- Endobronchial biopsy or resection
- Transbronchial biopsy or resection
- Mediastinoscopy (to biopsy mediastinal nodes or masses)
- Procedures which yield cytologic specimens
- Sputum analysis
- Bronchoalveolar lavage
- Transthoracic fine needle aspiration biopsy
- Transbronchial fine needle aspiration biopsy
- Work-up after diagnosis
- Contrast CT imaging of chest, liver and adrenal glands
- PET scan
- If CT finds metastases (advanced disease), then perform MRI for brain metastases and x-ray/bone scintigraphy for skeletal metastases
- Lung function test
- Non-small cell lung cancer (NSCLC)
- Accounts for 85% of cases
- Types
- Adenocarcinoma
- 40% of cases
- Idiopathic
- Peripheral
- SCC
- 20% of cases
- Smoking, etc.
- Central
- Large cell carcinoma
- 10% of cases
- Peripheral
- Adenocarcinoma
- Staging
- Stage I, II
- Tumor size < 7 cm
- No mediastinal invasion
- No lymph node involvement beyond ipsilateral hilar nodes
- No distant metastasis (M0)
- Stage IIIA
- Tumor size > 7 cm
- No mediastinal invasion
- Mediastinal lymph node involvement
- No distant metastasis (M0)
- Stage IIIB
- Any tumor size
- Mediastinal invasion
- Distant lymph node spread, but no distant metastasis (M0)
- Stage IV
- Any tumour size
- Any lymph node status
- Distant metastasis M1
- Stage I, II
- Treatment
- Generally, any tumor stage I – IIIb is potentially curable, while any other stage is palliative
- Surgery
- Lobectomy
- Wedge resection
- Pneumonectomy
- Chemotherapy
- Cisplatin
- Taxanes (paclitaxel)
- Radiotherapy
- External beam therapy and brachytherapy
- Stereotactic radiotherapy can be used for peripherally located inoperable tumors
- Emergency indications for radiation
- Superior vena cava syndrome
- Malignant spinal cord compression
- Brain metastasis
- Targeted therapy
- EGFR tyrosine kinase inhibitors – erlotinib, gefitinib
- ALK and ROS inhibitor – crizotinib
- ALK inhibitor – alectinib
- Anti-VEGF – bevacizumab
- Immunotherapy
- PD-1 inhibitors – pembrolizumab, nivolumab
- PD-L1 inhibitors – avelumab, atezolizumab, durvalumab
- Stage I – IIIa
- Surgery
- Postoperative chemotherapy in some cases
- Stage IIIb
- Radiochemotherapy
- Stage IIIc – IV
- Palliative
- Any combination of chemo, immune and targeted therapy, depending on histological type and molecular testing
- Squamous cell carcinoma
- Polychemotherapy
- Check for presence of PD-L1, if yes -> pembrolizumab
- Adenocarcinoma
- Check for KRAS, EGFR, ROS mutation and ALK/EML4 inversion
- If KRAS mutation -> chemotherapy
- KRAS mutation indicates poor prognosis
- If EGFR mutation -> EGFR inhibitor
- If ALK/EML4 inversion -> ALK inhibitor
- If ROS mutation -> ROS inhibitor
- Small cell lung cancer (SCLC)
- Accounts for 15% of cases
- Is a neuroendocrine tumor
- Has worse prognosis than NSCLC, but is very radio-and-chemosensitive
- Has a much higher turnover than NSCLC (tumor doubling every 50 days vs 200 days)
- Associated with paraneoplastic syndromes, like SIADH, Cushing syndrome, etc.
- Staging
- Because SCLC is radiosensitive its staging system is based on whether radiotherapy of the tumor is feasible
- “Limited disease” (corresponds to stages I – IIIB)
- 20% of cases at diagnosis
- Cancer spread confined to one hemithorax, and radiotherapy is therefore feasible
- “Extensive disease”
- 75% of cases at diagnosis
- Cancer spread beyond one hemithorax, and radiotherapy is therefore not feasible
- Treatment
- Chemotherapy
- Cisplatin + etoposide
- Prophylactic cranial irradiation
- Improves survival by killing brain metastases which are often already present but not visible on scans
- Limited disease – curative
- Radiochemotherapy
- Prophylactic cranial irradiation if remission is achieved
- Extensive disease – palliative
- Chemotherapy
- Prophylactic cranial irradiation in most cases
- Chemotherapy
15. Breast Cancer (BC)
- Epidemiology
- Most common cancer in women worldwide
- 2/3 of cases occur in women 55 or older
- Etiology
- Female gender
- Obviously the biggest risk factor
- Old age
- Family history
- 5 – 10% of cases are hereditary
- BRCA1 or BRCA2
- Women with 2 or more first-degree relatives with breast or ovarian cancer have more than 50% risk of developing BC
- Personal history (women who already have had breast cancer)
- Certain benign breast conditions
- Not breastfeeding
- Breastfeeding lowers BC risk
- Drinking alcohol
- Being overweight
- Physical inactivity
- Smoking
- Risk factors which cause increased oestrogen exposure
- Not having children
- Early menarche
- Late menopause
- Using hormone replacement therapy
- Female gender
- Genetic testing for hereditary breast cancer is indicated in:
- Women diagnosed with early stage breast cancer
- Genetic result will determine the treatment
- Women with metastatic breast cancer
- Genetic result will determine the treatment
- Healthy women who are suspected to have BRCA1 or BRCA2 mutation
- For example, healthy women with close relatives with breast or ovarian cancer
- Women diagnosed with early stage breast cancer
- Pathology
- Histological subtypes
- Invasive ductal carcinoma – 80% of cases
- Originates from a milk duct of the breast
- Invasive lobular carcinoma – 10% of cases
- Originates from a breast lobule
- Other – 10% of cases
- Invasive ductal carcinoma – 80% of cases
- Molecular subtypes
- Hormone receptor positive or negative
- Oestrogen receptor and/or progesterone receptor
- 60% are hormone receptor positive
- Hormone receptor positivity indicates better prognosis
- HER2 positive or negative
- HER2 positivity is due to amplification of the HER2 gene
- 20 % are HER2 positive
- HER2 positivity indicates a more aggressive cancer, but because we have targeted therapy against HER2 the prognosis of HER2 positive cancers is the same as HER2 negative
- Presence of HER2 can be detected by FISH (most accurate) or IHC
- If all three are negative the cancer is known as “triple negative”
- 15% are triple negative
- Triple negativity indicates poorer prognosis
- Hormone receptor positive or negative
- Histological subtypes
- Clinical features
- Many are asymptomatic – screening is important
- Lump in the breast
- Stages
- Early breast cancer
- Stage 0 – non-invasive
- Survival 100%
- Stage 1 – tumour is < 2 cm, no spread
- Survival 98%
- Stage 2 – tumour is > 2 cm, may have spread to nearby lymph nodes
- Survival 93%
- 30% of early BC relapse into metastatic BC
- Stage 0 – non-invasive
- Advanced breast cancer
- Stage 3 (locally advanced BC) – cancer spread beyond nearby lymph nodes but not to other organs
- Survival 72%
- Stage 4 (metastatic BC) – cancer spread to other organs
- Survival 22%
- Metastases to bone, brain, liver or lung
- Stage 3 (locally advanced BC) – cancer spread beyond nearby lymph nodes but not to other organs
- Early breast cancer
- Diagnosis
- Mammography
- Ultrasound of breast and nearby lymph nodes
- MRI
- For women with dense breasts, silicone implant or BRCA mutation
- Biopsy
- Core needle biopsy, FNAB, or excisional
- Mandatory for diagnosis
- Work-up after diagnosis
- Determination of histological and molecular subtypes
- Biopsy of suspicious lymph nodes
- CT chest, abdomen, pelvis
- Treatment
- Multidisciplinary teams (oncological teams) are used in the treatment of breast cancer
- Surgical treatment
- Some form of surgery is performed in all cases which are operable
- Mastectomy
- Radical or modified mastectomy
- Breast reconstruction can be performed in the same surgery as the mastectomy or at a later point
- Breast reconstruction can be achieved by implants, by autologous tissue implantation, or both
- Breast-conserving surgery
- Sometimes called lumpectomy
- Must always be followed up by radiotherapy
- Staging of axillary lymph nodes
- Must be performed during all surgeries
- By biopsy or lymph node dissection
- Radiotherapy
- Treatment planning is always based on CT to minimize heart and lung radiation
- The standard is to deliver whole-breast radiation
- Systemic therapy
- The molecular subtype determines the systemic therapy
- Chemotherapy
- Anthracycline
- Taxanes
- Hormonal therapy
- Hormonal therapy is indicated in most hormone positive patients
- Selective oestrogen receptor modulators
- Tamoxifen
- Aromatase inhibitors
- Fulvestrant
- Targeted therapy
- Anti-HER2
- For most HER2+ patients
- Trastuzumab
- PARP inhibitors
- For BRCA-positive advanced BC
- Anti-HER2
- Immune therapy
- Atezolizumab (PD-L1 inhibitor)
- For triple-negative breast cancer
- For early breast cancer (stage 0 – 2)
- Without BRCA mutation
- Breast-conserving surgery + adjuvant radiotherapy
- With BRCA mutation
- Mastectomy
- Prophylactic contralateral mastectomy
- Prophylactic bilateral salpingo-oopherectomy
- Without BRCA mutation
- For locally advanced breast cancer (stage 3)
- Neoadjuvant systemic therapy + surgical resection + adjuvant systemic therapy
- For metastatic breast cancer (stage 4)
- The cancer is generally not curable, but it is treatable
- Neoadjuvant systemic therapy + surgical resection and/or radiotherapy
- With BRCA mutation – PARP inhibitors
16. Cancer of the oesophagus and the stomach
- Oesophageal cancer
- Epidemiology
- Etiology
- GERD
- Smoking
- Poor diet
- Obesity
- Alcohol
- Pathology
- Adenocarcinoma
- Develops from Barrett’s oesophagus
- Rising incidence
- Squamous cell carcinoma
- The most common type, but incidence is declining
- The absence of tunica serosa in parts of the oesophagus causes oesophageal cancer to metastasize early
- Adenocarcinoma
- Clinical features
- Asymptomatic early
- Dysphagia
- Retrosternal pain
- Diagnosis
- Oesophageal endoscopy (oesophagogastroduodenoscopy)
- Best initial and confirmatory test
- Biopsy can be performed
- Oesophageal endoscopy (oesophagogastroduodenoscopy)
- Work-up after diagnosis
- Endoscopic ultrasound
- To assess T and N stage
- CT chest, abdomen
- To assess M stage
- Endoscopic ultrasound
- Treatment
- Surgery
- Endoscopic submucosal resection
- For very early localized disease
- Subtotal or total oesophagectomy
- Most commonly performed surgery
- Endoscopic submucosal resection
- Systemic therapy
- Chemotherapy
- Commonly used in oesophageal cancer
- FLOT
- Targeted therapy
- Trastuzumab – anti-HER2
- Immunotherapy
- Pembrolizumab
- Chemotherapy
- Radiotherapy
- Often used with chemotherapy
- Localized disease
- Surgery
- May be sufficient in early localized disease
- Neoadjuvant chemotherapy or radiochemotherapy
- Adjuvant chemotherapy
- Surgery
- Advanced disease
- Palliative
- Radiochemotherapy
- Targeted or immunotherapy
- Oesophageal stent placement
- Surgery
- Gastric cancer
- Epidemiology
- Male > female
- Old age
- High incidence in Korea, Japan
- Declining incidence in the west
- Etiology
- Foods rich in nitrates
- Salty food
- Nicotine use
- Atrophic gastritis
- H. pylori
- Gastric ulcers
- Pathology
- According to histological cell type
- Adenocarcinoma (90%)
- Signet ring cell carcinoma
- According to the Lauren classification
- Intestinal type
- Diffuse type
- At diagnosis 75% already have metastases
- According to histological cell type
- Clinical features
- Often asymptomatic in early stages
- General signs
- Iron deficiency anaemia
- Due to chronic blood loss
- Weakness
- Iron deficiency anaemia
- Abdominal pain
- Nausea, vomiting
- Painful, movable mass in epigastric region
- Diagnosis
- Faecal blood test
- Positive in some cases
- Gastroscopy (= upper endoscopy) with biopsy
- Biopsy confirms diagnosis
- Faecal blood test
- Work-up after diagnosis
- Endoscopic ultrasound
- Chest, abdominal and pelvic CT
- Bone scintigraphy
- If suspected bone metastasis
- Laparoscopy
- If suspected peritoneal carcinosis
- Treatment
- Surgery
- Radical gastrectomy and lymphadenectomy
- Systemic therapy
- Chemotherapy
- FLOT
- ECX
- Targeted therapy
- Trastuzumab – anti-HER2
- Ramucirumab – anti-VEGF
- Immunotherapy
- Pembrolizumab – anti-PD-1
- Chemotherapy
- Localized disease
- Surgery
- Both neoadjuvant and adjuvant chemotherapy or radiochemotherapy are often used
- Advanced disease
- Palliative
- Perioperative chemotherapy + surgery
- Targeted therapy and immunotherapy are options
- Surgery
- Epidemiology
17. Cancer of the pancreas and the liver
- Pancreatic cancer
- Epidemiology
- The 10th most frequent cancer, but the fourth leading cause of cancer-related death
- Etiology
- Smoking
- Chronic hepatitis
- Diabetes
- Obesity
- Pathology
- Responds poorly to chemotherapy
- Aggressive growth
- 2/3 in head
- 1/3 in tail
- 95% are adenocarcinomas
- Clinical features
- Asymptomatic early
- Belt-like epigastric pain
- Jaundice
- Weight loss
- Trousseau syndrome
- A paraneoplastic syndrome
- Causes superficial thrombophlebitis
- Courvoisier sign
- Enlarged gallbladder + painless jaundice
- Stages
- Resectable disease
- 15% present in this stage
- Median survival of 20 – 24 months
- Locally advanced (unresectable) disease
- 25% present in this stage
- Median survival of 8 – 12 months
- Metastatic disease
- 50% present in this stage
- Median survival of 6 – 12 months
- Overall 5-year survival for all patients is < 5%
- Resectable disease
- Diagnosis
- Abdominal US
- If positive -> CT with contrast
- CT with contrast or MRI
- Sufficient for diagnosis
- Also provides information for staging
- Biopsy is required to establish diagnosis
- However, if there is high clinical suspicion, a biopsy is not necessary
- Abdominal US
- Work-up after diagnosis
- CT chest
- PET
- Treatment
- Surgery
- Surgery is the only potentially curative treatment
- “Whipple procedure” (= pancreaticoduodenectomy)
- If pancreatic head tumour
- Distal resection
- If pancreatic body or tail tumour
- Systemic therapy
- Chemotherapy
- Gemcitabine
- 5-FU
- Albumin-bound paclitaxel
- Targeted therapy
- Erlotinib
- Chemotherapy
- Radiotherapy
- Not so frequently used
- Resectable disease
- Surgery + adjuvant chemotherapy or chemoradiotherapy
- If the tumour is borderline resectable -> neoadjuvant chemotherapy
- Non-resectable disease
- Palliative treatment
- Surgery to relieve bile tract obstruction, ileus, etc.
- Chemotherapy
- Enrolment into clinical trials
- Surgery
- Epidemiology
- Hepatocellular carcinoma
- Epidemiology
- Men > women
- Old age
- Most common in southeast Asia and Africa
- Etiology
- Cirrhosis
- 80% of HCC cases are preceded by cirrhosis
- Risk factors independent of cirrhosis
- Hep B, C
- Alcohol liver disease
- Non-alcoholic steatohepatitis
- Haemochromatosis
- Aflatoxin
- Cirrhosis
- Clinical features
- Usually asymptomatic
- Patient may have symptoms from underlying disease (cirrhosis, hepatitis)
- General symptoms
- Weight loss
- Weakness
- Abdominal pain
- Usually asymptomatic
- Diagnosis
- AFP
- Abdominal US
- Initial test
- Focal lesions in a cirrhotic liver are primary liver cancer until proven otherwise
- Abdominal CT
- Confirmatory test
- Liver biopsy
- Not necessary if definitive diagnosis is established with above tests
- Carries risk of bleeding and tumor spread
- Stages
- Many staging systems for HCC exist, and none are universally accepted
- It appears that POTE uses the Barcelona Clinic Liver Cancer (BCLC) staging
- This system stages the cancer based on liver function (Child-Pugh score), patient performance status (ECOG PS) and tumor morphology
- Liver function is scored according to Child-Pugh score
- This score checks multiple parameters that reflect liver function and gives points and a final score
- Child-Pugh A – good liver function
- Child-Pugh B
- Child-Pugh C – poor liver function
- Bilirubin
- Albumin
- Prothrombin time
- INR
- Presence of ascites
- Presence of hepatic encephalopathy
- This score checks multiple parameters that reflect liver function and gives points and a final score
- Very early stage (stage 0)
- Solitary lesion < 2 cm
- ECOG PS 0
- Child-Pugh A
- Early stage (stage A)
- Solitary lesion < 2 cm or 3 nodules < 3 cm
- ECOG PS 0
- Child-Pugh A or B
- Intermediate stage (stage B)
- Multifocal disease
- ECOG PS 0
- Child-Pugh A or B
- Advanced stage (stage C)
- Portal invasion or extrahepatic spread
- ECOG PS 1 – 2
- Child-Pugh A or B
- Terminal stage (stage D)
- ECOG PS 3 – 4
- Child-Pugh C
- Treatment
- Targeted therapy
- Sorafenib
- Multi protein kinase inhibitor
- Inhibits VEGFR, PDGFR, RAF, etc.
- Sorafenib
- Very early or early stage tumor
- Surgical resection
- Early stage tumor
- Liver transplantation
- Intermediate stage tumor
- TACE (transarterial chemoembolization)
- Advanced stage tumor
- Sorafenib
- Terminal stage tumor
- Palliative care
- Targeted therapy
- Prevention
- Patients with high risk for HCC (cirrhosis, hep B or C) should be regularly screening with AFP
- Epidemiology
18. Colorectal cancer
- Epidemiology
- 3rd most common malignancy
- 2nd most common cause of cancer-related death
- Average age – 60s
- 90% of CRC are sporadic, 10% are hereditary
- Etiology
- Old age
- Positive family history
- IBD
- Lifestyle factors
- Smoking
- Alcohol
- Obesity
- Diets high in meat, fat and low in fibre
- Low level of physical activity
- Hereditary CRC
- Familial adenomatous polyposis
- 100% risk of CRC
- Germline APC mutation
- Hereditary nonpolyposis colorectal cancer (Lynch syndrome)
- 80% risk of CRC
- DNA mismatch repair gene germline mutation
- Familial adenomatous polyposis
- Pathology
- Most CRC arise from adenomatous polyp
- Normal epithelium -> hyperproliferation -> adenomatous polyp -> invasive carcinoma
- Adenocarcinoma accounts for 95% of all CRC
- RAS, APC, p53 are all involved in carcinogenesis
- Incidence according to location
- Right-side colon – 1/4 of cases
- Left-side colon – 1/3 of cases
- Rectum – 40% of cases
- Metastases
- Colon cancer
- Mesenteric, paraaortic, retroperitoneal lymph nodes
- Liver
- Ovary (Krukenberg tumour)
- Lung
- Bone
- Rectal cancer
- Pararectal lymph nodes
- Liver
- Lung
- Bone
- Colon cancer
- Most CRC arise from adenomatous polyp
- Clinical features
- Often asymptomatic until late stages
- General symptoms
- Weight loss
- Fatigue
- Abdominal discomfort
- Right-sided carcinomas
- Iron deficiency anaemia
- Is very suspicious for CRC in elderly and postmenopausal women
- Melena
- Iron deficiency anaemia
- Left-sided carcinomas
- Changes in bowel habits
- Rectum and sigmoid
- Haematochezia
- Thin stools
- Rectal pain
- Stages
- Stage I
- T1 or T2, N0, M0
- Only invasion of submucosa
- Stage II
- T3 or T4, N0, M0
- Invasion of muscularis propria but N0, M0
- Stage III
- Any T, N1 or N2, M0
- Invasion of subserosa or beyond but M0
- Stage IV
- Any T, any N, M1
- Invasion or visceral peritoneum or adjacent organs
- Stage I
- Diagnosis
- Colonoscopy with biopsy
- Gold standard for diagnosis
- It is mandatory to survey the whole colon, as multiple cancers may be present simultaneously
- (Barium enema)
- May show a filling defect reminiscent of an apple-core
- (Digital rectal examination)
- Can only detect 10% of cancers
- Colonoscopy with biopsy
- Work-up after diagnosis
- Transrectal ultrasound – for T and N stage
- Chest, abdominal and pelvic CT
- For staging
- Lab
- Elevated CA19-9, CEA
- Histological evaluation
- Tumour grading
- Mismatch repair gene mutations
- HER2 mutation
- Treatment of colon cancer
- Surgical therapies
- Depends on exact localization of tumor
- Segment resection with intraabdominal anastomosis
- Rectal extirpation with colostomy
- Left or right hemicolectomy
- Lymphadenectomy
- Always performed, for pathologic staging
- Resection of metastases in the liver and/or lung
- One of the few cancers in which it is benificial to resect metastases
- Depends on exact localization of tumor
- Chemotherapeutical regimens
- Chemotherapy
- FOLFOX
- FOLFIRI
- Biological therapy
- Usually added in stage IV tumors
- Anti-VEGF – bevacizumab
- Anti-EGFR – cetuximab/panitumumab
- Targeted therapy
- Multi-tyrosine kinase inhibitors like regorafenib
- Chemotherapy
- Radiation therapies
- Radiation is not used for colon cancer (or any intraabdominal cancer) because the small bowel is very sensitive to radiation
- Radiation can be used for rectal cancer, as it lies in the pelvic region
- Stage I
- Curative treatment
- Surgical resection
- Stage II and III
- Curative treatment
- Surgical resection + adjuvant (6 months postoperative) chemotherapy
- 5-FU or FOLFOX
- Stage IV
- Palliative treatment
- Indicated in bleeding or bowel obstruction
- Surgical therapy
- Chemotherapy
- Biological therapy
- Surgical therapies
- Treatment of rectal cancer
- Radiation therapies
- Radiation can be used for rectal cancer, as it lies in the pelvic region
- Stage I
- Curative treatment
- Surgical resection
- Stage II and III
- Curative treatment
- Neoadjuvant radio-chemotherapy + surgical resection + adjuvant chemotherapy
- 5-FU
- Stage IV
- Palliative treatment
- Surgical treatment if bleeding or bowel obstruction
- Radiation therapies
19. Non-melanoma skin cancer
- Etiology
- UVA and UVB
- Cumulative, i.e. total sun exposure
- UVA and UVB
- Pathology
- UVA causes reactive oxygen species formation
- UVB
- Causes direct DNA damage
- Is more carcinogenic, but most of it is absorbed by the stratosphere
- Basal cell carcinoma
- Epidemiology
- Technically the most common cancer, but it is often excluded from data due to its low mortality and morbidity
- BCC accounts for 75% of all skin cancer
- Pathology
- Hedgehog pathway is often mutated
- Types
- Nodular BCC
- Superficial BCC
- Morpheaform BCC
- Naevoid basal cell carcinoma syndrome
- Autosomal dominant disease
- Multiple BCC in young age
- Bone and neurological malformations
- Etc.
- Treatment
- Surgery
- Surgical excision
- Primary treatment is almost all cases
- Radiotherapy
- If surgery is not an option
- Chemotherapy
- Only topical (5-FU)
- Alternatives for superficial and small BCCs
- Cryosurgery
- Photodynamic therapy
- Laser ablation
- Topical chemotherapy
- Topical imiquimod
- Targeted therapy
- Vismodegib or sonidegib
- Hedgehog pathway inhibitors
- For metastatic BCC or BCC which recurs after surgery
- Vismodegib or sonidegib
- Surgery
- Epidemiology
- Squamous cell carcinoma
- Epidemiology
- SCC accounts for 18% of all skin cancer
- Etiology
- UV
- Immunosuppression
- SCC is the most common cause of death in transplant patients
- HPV
- Precursor lesion
- Actinic keratosis
- Treatment
- Surgery
- Surgical excision
- Primary treatment is almost all cases
- Radiotherapy
- If surgery is not an option
- As adjuvant therapy if high-risk features are discovered during pathological staging
- Immune therapy
- For advanced SCC
- Cemiplimab – anti-PD-1
- Alternatives for superficial and small SCCs
- Cryosurgery
- Surgery
- Epidemiology
- Merkel cell carcinoma
- Cancer development related to immune system dysfunction
- Higher incidence and worse prognosis in immunocompromised
- Merkel cell polyomavirus
- Pinkish nodule on sun-exposed areas
- Treatment is surgical excision
- Cancer development related to immune system dysfunction
- Dermatofibrosarcoma protuberans
- Rare tumour, but the most common cutaneous sarcoma
- Translocation between chromosome 17 and 22
- Treatment is surgical excision
- Kaposi sarcoma (KS)
- Etiology
- Immunosuppression
- HHV8
- Types
- Classic
- Endemic (in Africa)
- Associated with non-HIV immunosuppression
- HIV related
- Nonepidemic variant
- Treatment
- Classic KS -> surgery or radiotherapy
- HIV-related KS -> treatment of AIDS alone may cause cancer regression
- KS associated with non-HIV immunosuppression -> changing immunosuppressing drug alone may cause regression
- Etiology
20. Melanoma
- Epidemiology
- Melanoma accounts for 5% of all skin cancer
- Etiology
- UVA and UVB
- Especially high doses over short period, in contrast to non-melanoma skin cancer
- Skin type I and II
- Sunburns in childhood
- Precursor lesions
- Giant (> 20 cm) congenital nevi
- Lentigo maligna
- Dysplastic nevi
- UVA and UVB
- Pathology
- BRAF mutation is found in 50%
- Breslow depth, mitotic rate and presence of ulceration on histology are important prognostic factors
- Types
- Superficial spreading melanoma
- 57% of cases
- Long horizontal spreading phase
- Nodular melanoma
- 21% of cases
- No horizontal spreading phase, just vertical spreading phase
- Poor prognosis
- Lentigo maligna melanoma
- Best prognosis
- Acral lentiginous melanoma
- Superficial spreading melanoma
- Stages
- Localized disease – cancer confined to primary site
- 84% of cases
- 98% 5-year survival
- Regional disease – cancer spread to regional lymph nodes
- 9% of cases
- 63% 5-year survival
- Metastatic disease – cancer has metastasized
- 4% of cases
- 22% 5-year survival
- Localized disease – cancer confined to primary site
- Diagnosis
- Dermoscope
- Full-thickness excisional biopsy
- Removes the entire tumour with a small margin of healthy skin around
- This is both diagnostic and therapeutic
- Check for BRAF mutation
- Treatment
- Surgery
- Immediate complete excision is the gold standard
- A sufficiently large safety margin (1 – 2 cm, depending on Breslow stage) must be used
- Chemotherapy
- Not used in melanoma
- Immunotherapy
- Checkpoint inhibitors are commonly used in advanced disease
- Ipilimumab – anti-CTLA-4
- Nivolumab, pembrolizumab – anti-PD-1
- Atezolizumab – anti-PD-L1
- Targeted therapy
- Vemurafenib – BRAF inhibitor
- MEK inhibitor (trametinib) is given simultaneously to prevent resistance
- Vemurafenib – BRAF inhibitor
- Localized disease
- Surgery is often enough
- Sentinel lymph node biopsy may be performed. If positive -> lymph node dissection and adjuvant immunotherapy or targeted therapy
- Regional and metastatic disease
- Surgery + adjuvant immunotherapy and/or targeted therapy
- Surgery
21. Soft tissue sarcomas and bone tumors
22. Nervous system tumors
- Epidemiology
- CNS malignancies account for 2% of adult malignancies, but 30% of childhood malignancies
- CNS metastases occur in 10% of cancer patients
- Secondary CNS tumours (metastases) are more common than primary
- Often from lung, breast, melanoma, etc.
- Most common CNS tumours
- Meningiomas
- Glioblastoma
- Most common in children – medulloblastoma
- Etiology
- HIV
- Nitrosoureas
- Head irradiation
- Hippel-Lindau syndrome
- Recklinghausen syndrome
- Pathology
- Location
- In adults – most tumours are supratentorial
- In children – most tumours are infratentorial
- Classification of primary CNS tumours
- Neuroepithelial tumours
- Gliomas (most common)
- Astrocytoma
- Ependymoma
- Oligodendroglioma
- Glioblastoma (grade IV)
- Embryonal tumours
- Primitive neuroectodermal tumor (PNET)
- Medulloblastoma
- Pinealomas
- Schwannoma
- etc.
- Gliomas (most common)
- Non-neuroepithelial tumours
- Meningiomas
- Tumours of the choroid plexus
- Germinomas
- Primary CNS lymphomas
- Pituitary adenomas
- etc.
- Neuroepithelial tumours
- Location
- Clinical features
- Seizures
- Most typical symptom of CNS tumour
- Focal neurological disturbances
- Personality changes
- Headache
- Vomiting
- Hypertension (Cushing reflex)
- Seizures
- Risk factors
- Grade
- Most important prognostic factor in CNS tumours
- Age
- Performance state
- Grade
- Diagnosis
- Imaging
- MRI with contrast (best)
- CT
- Imaging
- Treatment
- Neurosurgical intervention
- Very important in neurooncology because the tumour may have to be removed urgently to reduce symptoms
- Surgical resection is performed in nearly all CNS tumours
- Radiotherapy
- Most brain tumour patients receive some form of radiotherapy, often after surgery as adjuvant therapy
- External beam radiotherapy is much more common than brachytherapy
- Advanced techniques like 3DCRT, IMRT and radiosurgery are used to minimize damage to the brain
- Radiosurgery/stereotactic radiotherapy/gamma knife/Cyber knife therapy
- Used for lesions smaller than 3 cm
- Results similar to neurosurgery
- Craniospinal irradiation
- For tumours which often spread to CSF, like medulloblastoma
- The brain and spinal cord are simultaneously irradiated
- Whole brain radiotherapy (WBRT)
- Radiation to the whole brain
- Used for multiple CNS metastases
- Radiotherapy cause oedema -> increased ICP
- Prophylactic anti-oedema drugs like steroids, diuretics
- Chemotherapy
- Drugs has to penetrate BBB to be eligible for use against CNS tumours
- Temozolomide
- Most important drug for CNS tumours
- BCNU (carmustine)
- Methotrexate
- For CNS lymphomas
- For low-grade (I, II) glioma
- Neurosurgery alone
- For high-grade (III, IV) gliomas
- Neurosurgery (tumour debulking, as complete resection is rarely possible) + radiotherapy + chemotherapy (temozolomide)
- For primary CNS lymphoma
- Chemotherapy (methotrexate)
- Neurosurgery is not used as CNS lymphoma is diffuse rather than localized
- For meningiomas, mesenchymal tumours, etc.
- Neurosurgery
- Radiotherapy in case of unresectable or malignant tumours
- For secondary brain tumours
- Solitary tumour – surgery
- Few metastases – radiosurgery
- Multiple lesions – whole brain radiotherapy
- For spinal cord tumours
- Surgery, sometimes radiotherapy
- Neurosurgical intervention
23. Gynaecologic tumors
- Ovarian tumors
- Epidemiology
- Second most common gynaecological cancer
- Highest mortality of all gynaecological cancers
- Primarily a disease of postmenopausal women
- Etiology
- Family history
- BRCA mutation
- Risk factors which increase oestrogen exposure
- Early menarche
- Late menopause
- Obesity
- Nulliparity
- Pathology
- 90% are epithelial
- 10% are stromal or germ-cell
- Clinical features
- Often produces symptoms late
- Abdominal pains
- Ascites
- Symptoms of metastases into bladder, rectum, etc.
- Screening
- No effective screening for general population
- Screening is only for high-risk women
- Family history
- BRCA mutation
- Pelvic examination twice early
- Ultrasound
- Stages
- Stage I – cancer confined to ovary
- Rare
- Stage II – cancer has extended into pelvis
- Stage III – metastases outside pelvis
- Most patients are discovered at this stage
- 20 – 30% 5-year survival
- Stage IV – distant metastases
- The staging is pathological, meaning that the findings during exploratory surgery are what determine the stage
- 70% of cases are discovered in stage III or IV
- Stage I – cancer confined to ovary
- Diagnosis
- Transvaginal US
- Gold standard for suspected ovarian cancer
- Can show the presence of a mass, but cannot distinguish benign from malignant
- FNAB is never performed as it may cause spreading
- Diagnosis is generally made during exploratory surgery
- CA-125 serum marker
- Transvaginal US
- Work-up after diagnosis
- CT abdomen and pelvis
- Vaginal and abdominal US
- Treatment
- Surgery
- Exploratory surgery plays the biggest role in the treatment of ovarian cc and is both diagnostic and therapeutic
- Surgery always involves:
- Total extrafascial hysterectomy
- Bilateral salpingo-oophorectomy
- Pelvic and para-aortic lymphadenectomy
- Omentectomy
- Cytoreduction
- Performed in stage III, IV, when complete resection of the tumour is impossible
- Debulking of any lesions suspicious for metastases
- During the surgery visual assessment of the upper abdomen, peritoneal surfaces, mesentery and other abdominal organs is performed
- Any abnormal findings are biopsied and intraoperatively examined by a pathologist – if they are metastases, they are debulked
- This is part of the surgical staging
- Young, fertile, early-stage patients may receive fertility-preserving surgery instead
- This involves unilateral salpingo-oophorectomy instead of bilateral, and no hysterectomy
- Chemotherapy
- Ovarian cc is chemosensitive
- Chemo is always used after surgery as adjuvant therapy
- Except in stage Ia (rare)
- Paclitaxel + cisplatin/carboplatin
- Targeted therapy
- Bevacizumab
- Radiotherapy
- Rarely used due to low radiosensitivity
- Sometimes as palliative treatment
- Stage I – II
- Complete resection during exploratory surgery + adjuvant chemotherapy
- Stage III – IV
- Cytoreduction during exploratory surgery + adjuvant chemotherapy
- Surgery
- Follow-up
- Tumor marker CA-125 is used for follow-up
- Prognosis
- High incidence, high mortality
- High rate of recurrence
- Prognosis in stage III, IV depends on the degree of cytoreduction which is achieved
- Epidemiology
- Cervical cancer
- Etiology
- HPV 16, 18, 31, 33
- Smoking
- HIV
- Pathology
- Originates from the squamocolumnar junction
- 90% squamous cell
- Originate from the surface of the cervix (ectocervix)
- 10% adenocarcinoma
- Originate from the endocervix
- Worse prognosis than squamous
- Very rare
- Clear cell
- Small cell
- Clinical features
- Asymptomatic in early stages
- Abnormal vaginal discharge or bleeding
- Stages
- FIGO staging system
- Early cervical cancer
- Cancer which has not invaded the parametrium
- Includes stages Ia, Ib, IIa
- Locally advanced cancer
- Cancer which has invaded the parametrium
- Includes stages IIb and III
- Metastatic cancer
- M1
- Stage IV
- CT or MRI for staging
- Screening
- With pap smear
- Annually after sexually active age
- Low risk patients who has had two successive negative smears can perform it less frequently
- Diagnosis
- Pap smear
- High specificity but moderate sensitivity
- Scraping of ectocervix and endocervix with spatula or brush
- Also used for screening
- Colposcopy with biopsy
- Excisional biopsy (conization)
- Pap smear
- Work-up after diagnosis
- Imaging
- CT, MRI, PET
- Bimanual examination
- One finger in vagina and one finger in anus
- Used to palpate for spreading to parametrium
- Creatinine and urea
- Cervical cc can invade the ureters, causing kidney injury
- Cisplatin is nephrotoxic, so knowing the status of the kidney before therapy is important
- CT chest, abdomen, pelvis
- MRI pelvis
- Imaging
- Treatment
- Surgical
- Conservative surgery
- Extrafascial hysterectomy without pelvic adenectomy
- Wertheim operation
- Modified radical hysterectomy + pelvic lymphadenectomy
- Total removal of uterus and its ligaments
- Removal of pelvic lymph nodes on both sides
- Conservative surgery
- Radiation
- Radiation is very effective in all stages of cervical cc
- External beam radiation therapy (EBRT)
- The bladder is sensitive to radiation, so external radiation for cervical cancer should be limited to 50 Gy
- After 50 Gy has been delivered by ERBT, we switch to brachytherapy
- HDR brachytherapy with afterloading
- Chemotherapy
- Not often used in early cervical cancer
- Often used in combination with radiotherapy
- Cisplatin
- Most commonly used chemotherapy in cervical cc
- 5-FU sometimes added
- Microinvasive cervical cancer
- Corresponds to stage Ia1
- Conservative surgery
- Early cervical cancer
- No invasion of parametrium
- Wertheim operation or radiation
- Both surgery and radiation have equal probability of cure but different morbidity
- Postoperative radiochemotherapy, if features that signify high risk for recurrence are discovered during the surgery, like
- Lymph node spread
- Positive surgical margins
- Invasion into parametrium
- Other high-risk features
- Locally advanced cervical cancer
- Invasion of parametrium
- Radiochemotherapy
- Surgery is not used
- Stage IVb or recurrent cc
- Palliative treatment, if there are symptoms like pelvic pain, bleeding
- Radiotherapy or systemic therapy
- Surgical
- Etiology
- Endometrial cancer
- Epidemiology
- Most common gynaecological cancer
- Primarily occurs in postmenopausal women
- Etiology
- Unopposed oestrogen
- Obesity
- Nulliparity
- Infertility
- Diet
- Diabetes
- Hypertension
- Tamoxifen treatment
- Unopposed oestrogen
- Pathology
- Type I – endometrioid type
- In 80% of cases
- Grows slowly
- Hormone-sensitive
- Good prognosis
- Type II – other types
- Not hormone sensitive
- Not from endometrium
- Poor prognosis
- Type I – endometrioid type
- Clinical features
- Early signs and symptoms
- Screening is not needed
- Vaginal discharge
- Abnormal vaginal bleeding
- Early signs and symptoms
- Stages
- Stage I – cancer confined to the uterus
- 72% are diagnosed at this stage
- Stage II – cancer has spread to cervix
- Stage III – cancer has spread beyond uterus but still only in the pelvis
- Stage IV – distant metastases
- 3% are diagnosed at this stage
- Stage I – cancer confined to the uterus
- Diagnosis
- Fractional dilatation and curettage -> histology
- Gold standard for any abnormal bleeding
- Fractional dilatation and curettage -> histology
- Work-up after diagnosis
- MRI abdomen, pelvis
- Chest X-ray
- Treatment
- Surgery
- Total abdominal hysterectomy (TAH) with bilateral salpingo-oopherectomy
- Pelvic and para-aortic lymphadenectomy may also be performed
- Performed in all cases where possible
- The majority of patients with endometrial cancer present with early stage cancer, which is curable with surgery alone
- During the pathological staging, the cancer will be staged as low, intermediate or high-risk for persistence or recurrence, based on factors like
- High tumour grade
- Deep myometrial invasion
- Lymph node involvement
- etc.
- Low-risk disease does not require adjuvant therapy
- Surgery alone is curative in most low-risk patients
- Intermediate-risk disease will be treated by postoperative (adjuvant) radiotherapy
- High-risk disease will be treated by postoperative (adjuvant) chemotherapy
- Total abdominal hysterectomy (TAH) with bilateral salpingo-oopherectomy
- Radiotherapy
- Compared to cervical cancer, endometrial cancer is not so sensitive to radiotherapy
- Primary radiotherapy (without surgery) is reserved for inoperable or palliative patients
- Both external beam radiotherapy and intravaginal brachytherapy are used
- Chemotherapy
- Not commonly used in endometrial cancer
- Platinum-based drugs
- Hormonal therapy
- Progestins are the most commonly used hormonal agents
- Stage I and II
- Surgery (+ postoperative radiotherapy)
- Some patients with stage I may be candidates for hormonal therapy only, which preserves fertility
- Hormonal therapy is less effective than surgery, however
- Stage III and IV
- Treatment is often palliative
- Cytoreductive surgery when feasible
- Cytoreductive surgery increases survival
- Any combination of chemo, radio or hormonal therapy
- Surgery
- Epidemiology
24. Urologic and male genital cancers
- Prostate cancer
- Epidemiology
- The lifetime risk of prostate cancer is 1 in 8
- 64% of men between 60 and 70 have it
- Metastases
- Bone
- Liver
- Bladder
- Risk groups
- The risk for progression to metastatic disease is based on the following factors:
- TNM Stage
- Gleason score
- PSA level
- Diagnosis
- PSA
- New ways to measure PSA may increase the specificity of PSA for prostate cancer
- Free to total PSA radio
- Complexed PSA
- [-2]proPSA percent
- PSA velocity
- PSA density
- PSA is also used for follow-up
- New ways to measure PSA may increase the specificity of PSA for prostate cancer
- Biopsy
- For definitive diagnosis
- Transurethral, transrectal or transperineal
- PSA
- Work-up of diagnosed prostate cancer
- Histopathological examination of biopsy
- Grading according to the Gleason score
- Gleason 2 – 6 = low grade
- Gleason 7 = intermediate grade
- Gleason 8 – 10 = high grade
- Grading according to the Gleason score
- MRI
- Bone scan
- If high grade
- Histopathological examination of biopsy
- Progression of localized prostate cancer
- If cancer is not completely cured during the primary treatment, it will relapse
- Relapsed cancer is often treated with hormone therapy
- Hormone therapy initially helps, as the cancer at this stage is hormone-naïve or castrate-sensitive prostate cancer (CSPC)
- After some time, however, hormone therapy loses its efficacy. The cancer has become castration-resistant prostate cancer (CRPC)
- At this point the testosterone levels are still at castration levels, but the tumour has grown independent of testosterone
- This doesn’t mean that hormone therapy is useless
- CRPC is often metastatic
- Treatment
- Observational strategies
- Many cases of prostate cancer are better left untreated
- Watchful waiting
- Active surveillance
- Surgery
- Radical prostatectomy
- Pelvic lymphadenectomy may be performed
- Radiotherapy
- Prostate cancer requires a very high load of radiation for local control, up to 100 Gy total
- For this reason, EBRT and brachytherapy are often combined
- External beam radiation therapy
- Brachytherapy
- HDR or seeding
- Prostate cancer requires a very high load of radiation for local control, up to 100 Gy total
- Systemic therapy
- Hormonal therapy
- Androgen deprivation therapy (ADT)
- Orchiectomy (surgical castration)
- GnRH agonists or antagonists (chemical or pharmacological castration)
- Antiandrogens
- Never given alone – always combined with castration
- Abiraterone – testosterone synthesis inhibitor
- Enzalutamide – androgen receptor antagonist
- Side effects of hormonal therapy
- Erectile dysfunction
- Osteoporosis
- Metabolic syndrome
- Cognitive loss
- Androgen deprivation therapy (ADT)
- Chemotherapy
- Docetaxel or other taxanes
- Used only in castrate-resistant metastatic disease
- Immunotherapy
- Sipuleucel-T (a cancer vaccine)
- Bone-targeting therapy
- In cases of bone metastases
- Bisphosphonates
- Denosumab
- Radium-223
- This isotope mimics calcium and so is incorporated into areas of bone where bone metastases are forming
- Hormonal therapy
- Low-risk and intermediate-risk localized disease
- Observational strategies
- Surgery or radiotherapy
- High-risk localized and locally advanced disease
- ADT + ERBT or surgery
- Metastatic disease
- Hormone-naive
- ADT + antiandrogens
- Castration-resistant
- ADT + antiandrogens + chemo/immunotherapy
- Radium-223 is often used due to bone metastases
- Hormone-naive
- Observational strategies
- Epidemiology
- Bladder cancer
- Epidemiology
- Most common cancer of the urinary system
- Etiology
- Smoking
- Pathology
- Urothelial carcinoma
- Most common
- Squamous cell carcinoma
- Associated with schistosomiasis, chronic UTI and indwelling catheters
- Urothelial carcinoma
- Clinical features
- Painless gross haematuria
- Most common
- Irritative voiding symptoms
- Dysuria
- Increased frequency
- Urinary urgency
- Painless gross haematuria
- Stages
- Non-muscle invasive bladder cancer (NMIBC) = stage I
- Ta, T1 or Tis
- Muscle-invasive bladder cancer (MIBC) = stage II, III
- T2, T3, T4
- Metastatic bladder cancer = stage IV
- M1
- Non-muscle invasive bladder cancer (NMIBC) = stage I
- Diagnosis
- Urine cytology
- Cystoscopy
- Often combined with photodynamic diagnostics (PDD), which causes tumour cells to fluoresce
- Simple biopsies can be taken
- Transurethral resection of bladder tumour (TUR-B)
- Both diagnostic and therapeutic
- In all (non-metastatic) bladder cancers it’s important to know whether the cancer has invaded the muscular layer or not, which only TUR-B can tell
- Work-up after diagnosis
- If the cancer isn’t muscle-invasive, no further work-up is necessary
- CT urography
- These cancers are often multifocal, so the entire urinary tract must be examined
- CT abdomen and pelvis
- Treatment
- Surgery
- Transurethral resection of bladder tumour (TUR-B)
- The tumour and some surrounding bladder tissue are removed with a transurethral resectoscope
- This is both diagnostic and therapeutic
- After the resection, chemotherapeutical drugs or BCG are instilled into the bladder to reduce any residual cancer cells
- Radical cystectomy
- Bladder preservation therapy
- (Extensive) TUR-B followed by radiochemotherapy
- An alternative to radical cystectomy which preserves the bladder
- Transurethral resection of bladder tumour (TUR-B)
- Radiotherapy
- Inoperable tumours
- As part of bladder preservation therapy
- Systemic therapy
- Chemotherapy
- Gem/cis
- Immunotherapy
- Atezolizumab (anti-PD-L1)
- Pembrolizumab (anti-PD-1)
- BCG vaccine
- Intravesical BCG helps the immune system kill urothelial cancer
- Chemotherapy
- Non-muscle-invasive bladder cancer
- TUR-B alone is often enough
- Intravesical BCG or chemo is instilled after TUR-B
- Muscle-invasive bladder cancer
- Radical cystectomy or bladder preservation therapy
- Metastatic bladder cancer
- TUR-B is not performed
- Palliative
- Chemotherapy or immunotherapy
- Surgery
- Epidemiology
- Renal cell carcinoma (RCC)
- Etiology
- Smoking
- Obesity
- Family history
- Pathology
- These are adenocarcinomas which arise from tubular epithelium
- Urothelial cancers of the renal pelvis (etc.) don’t count as RCC
- 80 – 90% are clear cell carcinoma
- 10 – 15% are papillary carcinoma
- These are adenocarcinomas which arise from tubular epithelium
- Clinical features
- Mostly asymptomatic
- 50% are incidental findings on imaging
- Haematuria
- Anaemia
- Palpable flank mass
- Paraneoplastic syndromes
- Mostly asymptomatic
- Stages
- T1 – tumour < 7 cm
- T2 – tumour > 7 cm
- T3 – Tumour extends into renal vein or perinephric tissues
- T4 – Tumour extends beyond Gerota fascia
- Risk groups
- The risk for progression to metastatic disease is based on the following factors:
- TNM stage
- Tumour size
- Presence of histological necrosis
- Tumour grade
- Abnormal labs (LDH, Hb, Plt, etc.)
- Diagnosis
- CT abdomen with contrast
- Work-up after diagnosis
- CT/MRI thorax
- Treatment
- Surgery
- Nephron-sparing surgery (= partial nephrectomy)
- Preferred, when feasible
- Radical nephrectomy
- Nephron-sparing surgery (= partial nephrectomy)
- Radiotherapy
- Stereotactic radiotherapy
- For inoperable patients
- Systemic therapy
- Targeted therapy
- Anti-VEGF
- Bevacizumab
- mTOR inhibitors
- Everolimus
- Tyrosine kinase inhibitors
- Sunitinib, sorafenib, etc.
- Cabozantinib
- Pazopanib
- Anti-VEGF
- Immunotherapy
- Nivolumab (anti-PD-1)
- Ipilimumab (anti-CTLA-4)
- Targeted therapy
- Localized disease
- Surgery
- Metastatic disease
- Low or intermediate risk -> targeted therapy
- High risk -> immunotherapy
- Surgery
- Etiology
- Testicular cancer
- Epidemiology
- Most common cancers in men 15 – 35
- Surprisingly rare in women
- Etiology
- Cryptorchidism
- Klinefelter syndrome
- Pathology
- Seminomas (50%)
- Very radiosensitive
- Non-seminomas (50%)
- Often a combination of embryonal carcinoma, yolk sac, choriocarcinoma, etc.
- Moderately radiosensitive
- Seminomas (50%)
- Clinical features
- Mostly asymptomatic
- Testicular lump
- Stages
- Limited disease – cancer limited to testicles
- Locally advanced disease – retroperitoneal lymph node involvement
- Metastatic disease – M1
- Diagnosis
- Testicular ultrasound
- Often enough to establish the presence of malignant tumour
- Tumor markers
- LDH
- hCG
- AFP
- Orchidectomy
- Both diagnostic and therapeutic
- Testicular ultrasound
- Work-up after diagnosis
- CT chest, abdomen, pelvis
- Treatment
- Surgery
- Radical (inguinal) orchidectomy
- Performed in all cases
- Retroperitoneal lymph node dissection (RPLND)
- Para-aortic lymph nodes are most commonly affected
- Radical (inguinal) orchidectomy
- Radiotherapy
- External beam radiotherapy
- Generally only used in seminomas, not non-seminomas
- Radiotherapy is less and less used, chemo is more and more preferred instead
- Chemotherapy
- Cisplatin
- Etoposide
- Bleomycin
- Localized disease (stage I)
- Orchidectomy
- Active surveillance
- In low-risk localized disease
- Adjuvant chemotherapy
- In intermediate and high-risk localized disease
- Locally advanced disease (stage II)
- Orchidectomy + adjuvant radio (targeting retroperitoneal lymph nodes) or polychemotherapy or RPLND
- Metastatic disease (stage III)
- Orchidectomy + polychemotherapy
- Surgery
- Epidemiology
Hello 🙂 I think the Krukenberg tumor is arising from gastric ccs only, not CRC as you put in the topic (not 100% sure)
That is in fact not correct, Krukenberg can arise from anywhere but classically from gastric cancer.
😄