Treatment- Chemotherapy, Radiotherapy Flashcards

1
Q

What are the stages of tumour growth?

A

Dysplasia
Cancer in situ
Invasion (detection threshold)
Onset of metastases

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2
Q

Cancer treatment- and what percentage for cure

solid tumours- not haematological

A

Chemotherapy (10%)
Radiotherapy (40%)
Surgery (50%)

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3
Q

What is the biological basis for radiotherapy

A

Damages DNA, destroying their ability to repair/ reproduce

Cancer cells have less ability to repair the damage than normal cells (tolerance)

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4
Q

How does radiotherapy protect normal healthy cells?

A

Fractionation
Dividing the total dose into daily fractions
Allows normal tissues to repair themselves better longer-term whilst ensuring damage to cancer cells

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5
Q

What beams are used in radiotherapy?

A

High powered Xrays
Millions MV of volts
The high beam x-ray is absorbed equally by bone and tissue

Electrons - skin
Protons- good for radiotherapy in sensitive areas (such as spine?)

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6
Q

What is palliative radiation therapy?

A

not curative or radical
relieve pain from bone metastases

spinal cord compression
vascular compression (SVC syndrome)
bronchial obstruction
bleeding from GI / gynaecological tumours
oesophagus obstruction (Cancer is causing an obstruction of food so this can provide some relief) (Alternative use is a stent)

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7
Q

Explain use of Palliative CT

A

DRR- computer removes the bone density imaging from the CT scan to degenerate an Xray which helps orientate and plan the radiation

to hit the target- treat one vertebra above and one below.

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8
Q

What dose is used in Palliative fractionation (Gy)

A

a small number of large fractions (the overall total dose is not high enough to cause significant damage)
(patient will not live long enough to get long term side effects- palliative)

single 8Gy (gray)
200G 5fractions
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9
Q

What dose is used in Radical / curative fractionation (Gy)

A

high dose spread over many fractions

65Gy 30fractions
70Gy 35fractions

longer duration of acute side effects but lower long term damage to organs

put in the same position for weeks. reference marks / tattoo.

CT simulation images are fused with MRI and PET to improve identification of cancer location.

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10
Q

What is a multi-leaf collimator?

A

plates that can be controlled by a computer. move them and ensure a treatment field which conforms to the SHAPE of cancer. (e.g square= catch healthy cells and damage them)

*avascular necrosis of head of the femur.

e.g. circle around the bladder, rectum for prostate cancer. volume in the bladder will change the prostate shape.
must be below 50 Gy.

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11
Q

Intensity Modulated Radiotherapy (IMRT)

A

A beam that arcs around the patient which avoids the critical structures and reduces side effects.

uses a changing beam intensity to achieve that.

uses MLC (multi-leaf collimator)

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12
Q

How does a proton beam design work?

A

When the beam enters the body, it delivers the dose at the same place. There is no exit dose because there is no energy left in the beams. Reduces side effects.

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13
Q

What are some common radiation side effects?

A
  • Breast- swelling, skin redness
  • Abdo- nausea, vomiting, diarrhoea
  • Chest- cough, SOB, oesophagal irritation
  • Head and neck- taste alt, dry mouth, mucositis, skin red
  • Brain- hair loss, scalp redness, long term demyelination (somelence= dopey 4-6 weeks after tx)
  • Pelvis- diarrhoea, cramping, urinary frequency, vaginal irritation
  • Prostate- impotence, urinary symptoms, diarrhoea
  • Fatigue.

*chemotherapy - systemic side effects.

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14
Q

Neoadjuvant induction treatment (chemo)

A

Curative/radical treatment categories:

  • neo-adjuvant/induction tx = before the main treatment (shrinks- reduces the area so less risk of side effects to nearby structures with radiotherapy) (decreases the area of hypoxic tissue, increasing your chance of cure).
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15
Q

What are the four main types of curative/radical chemotherapy?

A
  • neo-adjuvant / induction
  • primary - unusual for solid tumours
  • adjuvant = after the main treatment
  • concurrent = with Radiotherapy (RT)
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16
Q

Concurrent chemotherapy

A

Chemotherapy given the same time as radiotherapy. Improves survival by 5-8%
Makes side effects worse but no long term difference in side effects
70-75% of the full dose of chemotherapy

17
Q

Adjuvant chemotherapy

A

Chemo after surgery/ treatment

4/100 survive?

18
Q

Palliative chemotherapy

A

Improve the quality of life (not curative)

Shrink cancer and improve symptoms

19
Q

How does chemotherapy work?

A

Affects the replicating cell cycle
G=- cancer cell is resting phase (resistant to chemotherapy)
G1= interphase
S= DNA synthesis
G2= DNA synthesis ceases, protein and RNA synthesis, mitotic spindle production
M= mitosis, genetic material segregated into daughter cells.

chemo kills of rapidly dividing cells (caner) and healthy rapidly dividing cells (gut surface= diarrhoea, bone marrow) so leave a gap for the normal tissues to recover. this however does give time for cancer cells to recover.

in each cycle, there are less ‘vulnerable’ cancer cells and more resistant ones

20
Q

explain the cell cycle

A

G=- cancer cell is resting phase
G1= interphase
S= DNA synthesis
G2= DNA synthesis ceases, protein and RNA synthesis, miotic spindle production
M= mitosis, genetic material segregated into daughter cells.

21
Q

Resistance to chemotherapy

A

Acquired
?
?
Pharmacological (gut) (do not absorb oral drugs) (liver)
Biochemical: development of drug-resistant proteins. (body has evolved to remove toxic proteins)

22
Q

Targeted therapies

A

target specific molecules involved with tumour growth (surface) (secondary messenger pathways)

interfere with cell proliferation
focus on proteins involved in cell signalling
mabs work on cell surface: (mabs= monoclonal antibodies: desoumab, transtuzumab)
nibs works on secondary messenger pathways (penetrate the cytoplasm/nucleus): nibs (erlotinib, gefitinib)

induce programme cell death (apoptosis)

23
Q

Class 1: Tyrosine kinase inhibitors

A

enzymes responsible for activation of proteins by signal transduction cascades

24
Q

Class 2: Anti-angiogenic therapies

A

Drugs that block the growth of blood vessel tumour. inhibit angiogenesis.

25
Q

Class 3: immune modulator

A

targeted therapies which help the immune system destroy cancer cells.
rituximab (MAB-CD20- B cell NHL)
Ipilimumab (MAB- cytotoxic T lymphocyte associated antigen 3- CTLA-$ melanoma

gets the t-cells do not be down-regulated by the cancer cells.

*iplimumab toxicity!
cause auto immune attack of any organ in the body. lots of gas under the diaphragm- perforation
auto immune colitis causing a toxic mega-colon from ipilimuab causing perforation