Oncology - General Flashcards

1
Q

Neo-adjuvant Chemo - Indications

A

Pre-operative

Make tumour smaller to decrease extent of surgery
Minimise occult metastasis

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2
Q

Primary Chemo

A

Initial treatment if unoperable tumour

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3
Q

Adjuvant

A

Following surgery

Treat occult mets

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4
Q

Adjuvant - Used for what cancers?

A

Breast

Colorectal

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5
Q

Palliative

A

Alleviation of symptoms, no intention of cure

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6
Q

Curative - What cancers?

A

Germ cell

Hodgkins

Non-hodgkins

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7
Q

Prophylactic Example

A

Tamoxifen for in situ breast cancer

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8
Q

Three Principles of Chemo Combo Therapy

A
  1. Different classes have different actions: synergism
  2. less chance of drug resistance
  3. Dose maintained due to differing toxicities in different drugs
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9
Q

Chemo - Cycles

A

Every 3-4 weeks

Allows recovery of normal cells e.g. stem cells and GI tract

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10
Q

Chemo - Treatment length

A

Max effectiveness = 6 months

Then resistance and increased toxicity

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11
Q

Conventional Dose - Involves?

A

Outpatient setting, tolerable side effects

Use drug known to be toxic against specific Ca

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12
Q

High Dose - Involves?

A

May need support e.g. bone marrow rescue

Justified if high chance of cure

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13
Q

High Dose - Curative?

A

Hodgkin’s Disease

Ewing’s sarcoma

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14
Q

Maintenance Chemo?

A

Only if good evidence

e.g. childhood leukaemia - for 18 months following remission

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15
Q

Chemo - Oral Route

A

No hospital

Reduced toxicity

Only certain drugs

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16
Q

Chemo - Oral Drugs

A

Cyclophosphamide

Tamoxifen

17
Q

Chemo - IV route

A

Majority

By infusion bolus

Lines - Central, tunnelled (PICC)

18
Q

Chemo - Regional examples

A

Intravesical - bladder Ca

Intraperitoneal - transcolaemic e.g. ovarian

Intra-arterial e.g. hepatic artery for liver mets

19
Q

Chemo - Dose calculation

A

Dubois and Dubois Surface area calculation

Carboplatin from renal function!

20
Q

Radiotherapy - Dose

A
Unit Gray (Gy)
Increased dose if radical treatment
21
Q

Radiotherapy - Factors affecting success

A
  1. Treatment dose/total volume/overall treatment time
  2. Comorbitities (diabetes IBD)
  3. Radiosensitivity of tumour (Seminoma and hodgekins = very sensative)
22
Q

Delivery - GTV

A

Gross tumour volume

  • Directly attacked
23
Q

Delivery - CTV

A

Clinical target volume

allows margin for microspread of tumour

24
Q

Delivery - PTV

A

Planned target volume

allows margin for patient movement

25
Q

RT - Total target area

A

Gross + Clinical + Planned target volume

26
Q

RT - Side Effects (Acute)

A

After 5-10 treatments, peaks following completion

Reversible but require management

E.g.

  • Oral mucositosis
  • Diarrhoea
  • Local skin reaction (can be v. severe)
27
Q

RT - Side Effects (Chronic)

A

More than 3 months after course ends, maybe years
- irreversible and progressive

E.g.

  • Lung fibrosis
  • Skin atrophy
  • Infertility
28
Q

RT - Malignancy Risk

A

Increased risk if good prognosis Ca, as higher dose given

Breast cancer = 4 in 10000 Ca after RT

29
Q

RT - In pregnancy?

A

Teratogenic, avoid!

30
Q

Bracytherapy

A
  1. Intracavity
    - Uterus/cervix
  2. Interstitial
    - Prostate, into tumour directly
31
Q

Radioisotopes

A

Radioactive iodine, thyroid Ca

  • Selective to thyroid
  • Must stay in lead room for protection of others
32
Q

Markers - CEA

A

Colorectal

Increased in
- Smokers, IBD, Hepatitis, Pancreatitis, Gastritis

33
Q

Markers - Ca-125

A

Ovarian Ca (82% will have high)

Raised in pancreatic, lung, colorectal and breast Ca.

34
Q

Markers - AFP

A

High in teratoma, hepatocellular Ca

  • usually undetectable after age of 12 months
35
Q

Markers - bHCG

A

Non-seminomatous Ca

36
Q

Markers - PSA

A

Prostate Ca and BPH,

may rise in DRE, UTI etc.

Can be used to monitor response to treatment

37
Q

RECIST - Treatment response on imaging

A

CR - Complete response (no tumour seen)

PR - Partial (shrunk by >30%)

SR - Stable (increase <20, Decrease less than 30%)

PD - Progressive >20% increase or new lesions