Oncology Flashcards

1
Q

Give 5 examples of inherited conditions that can cause cancer?

A
  1. neurofibromatosis (6+ cafe au lait spots)
  2. adenomatous polyposis coli
  3. Von Hippel Lindau syndrome
  4. Li Fraumeni syndrome (mutation in p53)
  5. BRCA 1 and 2
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2
Q

How can chemicals cause cancer?

A

damage cellular DNA and produce mutations in oncogenes and tumour suppressor genes

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3
Q

which type of cancer can vinyl chloride cause?

A

angiosarcomas

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4
Q

which type of cancer does benzene cause?

A

leukaemia

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5
Q

Which type of cancer do aromatic amines cause?

A

bladder

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6
Q

which type of cancer does wood dust cause?

A

nasal adenocarcinoma

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7
Q

How does radiation cause cancer?

A

increases DNA damage leading to the accumulation of mutations in tumour suppressor and oncogenes

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8
Q

How does HPV cause cancer?

A

produces E6 which inctivates p53

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9
Q

which types of cancer does HPV cause?

A
  • cervical
  • anal
  • oropharyngeal
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10
Q

Which two strains of HPV are the cancerous ones?

A
  • 16 and 18
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11
Q

which type of cancer can EBV cause?

A

non-hodgkins lymphoma

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12
Q

Which type of cancer is hCG (as a tumour marker) raised in?

A

Testicular

non-seminomatous testicular cancer
seminoma

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13
Q

Which benign conditions can lead to a raise in PSA?

A
  • BPH
  • rectal exam
  • prostatitis
  • UTI
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14
Q

what is the common clinical use of carcinoemryonic antigen (CEA) tumour marker?

i.e. which cancer?

A

colorectal cancer

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15
Q

Which conditions is CA125 raised in?

A
  • ovarian cancer
  • pregnancy
  • pancreatic ca
  • lung cancer
  • colorectal cancer
  • breast cancer
  • endometriosis
  • PID
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16
Q

which cancer is AFP raised in?

A

Hepatocellular carcinoma

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17
Q

For staging cancer which 2 areas do you use CT for and which 4 areas do you use MRI for?

A

CT:

  • chest
  • abdomen

MRI

  • bone
  • soft tissue
  • pelvis
  • posterior cranial fossa
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18
Q

Using imaging- what is the definition of a partial response to treatment?

A

all lesions shrunk by >= 30%

disease is still present

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19
Q

Using imaging- what is the definition of stable disease?

A

<20% increase in size OR

<30% decrease in size

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20
Q

Using imaging- what is the definition of progressive disease?

A

new lesions

lesions increased in size by >20%

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21
Q

what is CT/ what images does it take?

A
  • rotating x-ray tube

- axial cross-sectional images

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22
Q

What is the principle concern with CT?

A

the dose of radiation

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23
Q

MRI is the golf standard for which 4 types of tumours (locations)?

A
  • neurospinal tumours
  • rectal tumours
  • prostate tumours
  • MSK tumours
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24
Q

What is the principle concern with MRI?

A
  • magnetic field

- therefore check pacemakers, metal in body, equipment in the area

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25
Q

What is ultrasound/ how does it work?

A

high frequency sound waves

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26
Q

give 4 uses of ultrasound in cancer care?

A
  1. detecting mets in solid visceral abdo organs
  2. doppler–> assess tumour blood flow
  3. soft tissue
  4. guidance of biopsies and procedures
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27
Q

What is the principle behind bone scintography and what is it most commonly used for?

A
  • radioisotope labelled drugs given IV

- main investigation for skeletal mets

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28
Q

What type of images do PET scans produce and what tracer is commonly used?

A
  • produces functional images
  • tracer used in FDG-18 ( fluorine 18 deoxyglucose)
  • PET has potential to differentiate between malignant and benign pathologies
  • PET usually combined with CT to map functional images to detailed anatomy
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29
Q

4 advantages to screening programmes?

A
  1. reduction of mortality
  2. less radical treatment ( decreases morbidity)
  3. saving health resources by increased cure rates
  4. reassurance given by a negative test
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30
Q

6 disadvantages to screening programmes?

A
  1. increased anxiety if no effective intervention possible
  2. over investigation of false positive cases
  3. over treatment of borderline cases
  4. false reassurance from a false negative
  5. possible harmful side effects of the screening test
  6. cost of screening a large population
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31
Q

for which 3 cancers are there screening programmes in place?

A
  1. cervical
  2. breast
  3. colorectal
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32
Q

What is the current cervical cancer screening programme?

A
  • cervical smears for all women between 25-64
  • every 3 years for women 25-49
  • every 5 years for women 50-64
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33
Q

What is the current breast cancer screening programme?

A
  • mammogram every 3 years for women aged 50-70

- screen younger patients if high risk e.g. FHx

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34
Q

What is the current colorectal cancer screening programme?

A
  • foecal occult blood (FOB) every 2 years 60-69
  • 69-74 can request screening kit
  • high risk patients reviewed regularly e.g. UC
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35
Q

is there a screening programme for prostate cancer?

A
  • no

- but informed choice programme with PSA

36
Q

4 different types of biopsy that can be done to diagnose cancer?

A
  1. fine needle aspiration cytology
  2. tru-cut needle biopsy (under local)
  3. incisional biopsy
  4. excisional biopsy
37
Q

what is cytoreductive surgery?

A

reducing the bulk of the disease

38
Q

What is radiation? when is it used?

A
  • use of ionising radiation in the management of cancer
  • has curative potential in the absence of mets
  • can be used in a neo-adjuvant, adjuvant or palliative setting
39
Q

how is radiotherapy delivered most commonly in UK?

A
  • external beam radiotherapy
  • using photons/ x-rays
  • 3D conformal radiotherapy ( individual tumour mapping to target the tumour)
40
Q

What are the units of radiotherapy?

A
  • gray units (Gy)

- given in small fractions rather than a large single dose

41
Q

What is the mechanism of action of radiotherapy? (4 steps)

A
  1. high energy short wavelength X-rays by a linear accelerator
  2. X-rays penetrate deep into body tissue (sparing overlying skin)
  3. X-rays produce secondary electrons and free radicals (cause DNA damage)
  4. cancer cells defective at repair–> mitotic or apoptotic cell death
42
Q

What 3 things does the success vs toxicity of radiotherapy depend on?

A
  1. treatment issues ( total dose, total volume, overall treatment time)
  2. co-morbidities (diabetes, IBD, smoking)
  3. radio-sensitivity of the cancer
43
Q

What three measurements are taken during a planning CT for tumour mapping before radiotherapy?

A
  1. Gross tumour volume (GTV)
  2. Clinical target volume (CTV)
  3. Planning target volume (PTV)
44
Q

What is the gross tumour volume?

A
  • The tumour is delineated on each CT slice it appears on

- so the tumour on each CT slice

45
Q

What is clinical target volume?

A
  • added margins to allow for microscopic disease spread
46
Q

What is the planning target volume?

A
  • a further margin is added to allow for daily variations in patient and tumour position
47
Q

Is radiotherapy safe in pregnancy?

A

NO

it is teratogenic

48
Q

When do the acute side effects of radiotherapy usually develop?

A
  • during treatment

- usually after the first 5-10 fractions

49
Q

Why do you get the acute side effects of radiotherapy?

A
  • due to damage of normal tissue and the ability of normal cells to repair damage
  • therefore usually completely resolve once treatment has finished
50
Q

3 examples of acute side effects of radiotherapy?

A
  1. localised skin reaction
  2. oral mucositis
  3. diarrhoea
51
Q

When do the late side effects of radiotherapy usually develop and are they reversible?

A
  • usually develop at least 3 months after radiotherapy (can be longer)
  • often irreversible and may get worse over time
52
Q

Why do the late side effects of radiotherapy occur?

A
  • some of the damage to normal cells cannot be repaired

- partly due to development of fibrosis and blood vessel damage within the irradiated tissue

53
Q

what are 4 examples of late side effects of radiotherapy?

A
  1. lung fibrosis
  2. skin atrophy
  3. infertility
  4. risk of second malignany
    - radiotherapy itself is carcinogenic
    - risk is significantly greater in younger patients
54
Q

What is brachytherapy?

A
  • radiation sources placed within or close to tumour
  • localised high dose (intercavity or interstitial)
  • prostate, gynae, oesophageal, head and neck
  • patient is radioactive (risk to others)
55
Q

What is chemotherapy?

A
  • systemic treatment of cancer using cytotoxic agents
56
Q

What is the MOA of chemotherapy?

A
  • most target DNA indirectly or directly
  • agents are preferentially toxic towards actively proliferating cells
  • thus rapidly dividing tumours respond best
57
Q

7 indications/ settings of chemotherapy?

A
  1. radical- curative intent
  2. primary- alone for cure
  3. neo-adjuvant
  4. adjuvant
  5. chemoradiation
  6. palliative
  7. high dose- with bone marrow transplant for stem cell support
58
Q

What does the term ‘cycle’ mean in chemotherapy?

A

e.g. docetaxel IV day 1 every 21 days

59
Q

What does the term ‘course’ mean in chemotherapy?

A

the planned number of cycles

60
Q

How do you calculate the dose for chemotherapy?

A
  • using body surface area most commonly
  • DuBois formula
  • also according to renal function
61
Q

immediate side effects of chemotherapy?

A
  • nausea and vomiting
  • myelosuppression
  • diarrhoea and constipation
  • alopecia
  • ototoxicity
  • neuropathy
  • nephrotoxicity
  • arrhythmia
  • transient rise in LFTs
  • skin changes (pigmentation)
  • lethargy
  • myalgia
62
Q

long term complications of chemotherapy?

A
  • second malignancies
  • reduced fertility
  • pulmonary fibrosis
  • cardiac fibrosis
63
Q

What is the definition of neutropenic sepsis?

A
  • absolute neutrophil count of <1 x10 9 /L

AND

  • single temperature over 38.5 OR
  • sustained temperature over 38 OR
  • clinical signs
64
Q

How many days post chemo is neutropenic sepsis more common?

A

7-14 days post chemo

65
Q

Which examinations should you avoid in a person with suspected neutropenic sepsis?

A
  • rectal

- vaginal

66
Q

Investigations for a person with suspected neutropenic sepsis?

A
  • BUFALO
  • FBC, U and Es, LFTs
  • paired blood cultures (x2 anaerobes and aerobes, culture all lines or if no lines –> 2 peripheral cultures)
  • swabs
  • sputum culture
  • urinalysis and MSU
  • stool analysis and culture
  • CXR if respiratory signs (? atypical pneumonia serology)
67
Q

Which type of organism is more likely to cause neutropenic sepsis (70%)?

A

Gram positive

68
Q

Give three examples of gram positive organisms that may cause neutropenic sepsis?

A
  • staph aureus
  • coagulase negative staph
  • alpha and beta haemolytic strep
69
Q

What is the management of neutropenic sepsis?

A

Broad spec antibiotics (trust guidelines) within 1 hr

  • e.g. tazocin (tazobactam and piperacillin)
  • continue until afebrile for 72 hours OR
  • 5 days course and neutrophils >0.5 x 10 9
70
Q

What is the MASCC score?

A

a scoring system for identifying low-risk (of complications) cancer patients with febrile neutropenia

71
Q

Which 5 cancers are more commonly associated with metastatic cord compression?

A
  • prostate
  • breast
  • lung
  • myeloma
  • lymphoma
72
Q

Which region of the spinal cord does metastatic cord compression most commonly affect?

A

2/3 in the thoracic spine

73
Q

Presentation of MSCC?

A
  • back pain (alone in 90%)
  • leg weakness
  • sensory loss
  • bowel/bladder dysfunction (incontinence or retention)
  • saddle anaesthesia
  • loss of anal tone
74
Q

Management of metastatic spinal cord compression?

A
  • lie flat
  • 16mg dexamethasone (PPI cover)
  • urgent MRI full spine within 24hrs
  • contact local spinal cord co-ordinator
  • consider neurological intervention
  • ? radiotherapy
75
Q

3 broad causes of superior vena cava obstruction?

A
  1. extrinsic compression
  2. thrombosis
  3. invasion
76
Q

What is the most common cause of SVCO and by which two types of cancer?

A
  • extensive lymphadenopathy in upper mediastinum

- lung and lymphoma

77
Q

5 benign causes of SVCO?

A
  • goitre
  • mediastinal fibrosis
  • infection (TB)
  • aortic aneurysm
  • thrombus
78
Q

Presentation of SVCO?

A
  • breathlessness
  • headache - worse on coughing, “fullness”
  • facial/ neck/ arm swelling
  • distended neck and chest veins
  • cyanosis
  • visual disturbance
79
Q

Investigations for SVCO?

A
  • CXR
  • contrast CT
  • consider: tumour markers, bronchoscopy, OGD (if oesophageal cancer suspected, biopsy)
80
Q

Management of SVCO?

A
  • 16mg dexamethasone (PPI cover)

- depending on the cause (stenting under radiological guidance, radiotherapy, chemotherapy, LMWH if thrombosis)

81
Q

why do you get hypercalcaemia in cancer?

A
  • cancer of bones or bone mets

- due to an imbalance between bone resorption and calcium excretion

82
Q

What is the most common cause of hypercalcaemia (before cancer)?

A

primary hyperparathyroidism

83
Q

Cancers that cause hypercalcaemia?

A
  • NSCLC
  • breast
  • prostate
  • renal cell carcinoma
  • myeloma/ lymphoma
84
Q

Key investigation for hypercalcaemia?

A
  • serum calcium

- CORRECTED FOR SERUM ALBUMIN

85
Q

Presentation of hypercalcaemia?

A

General

  • dehydration
  • weakness
  • fatigue
  • bone pain

CNS

  • confusion
  • seizures
  • proximal neuropathy
  • hyporeflexia
  • coma

GI

  • weight loss
  • N and V
  • abdo pain
  • constipation
  • ileus
  • dyspepsia