Cancer Chemotherapy Flashcards

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1
Q

What is the fractional cell kill hypothesis?

A

The balance between tumour cells and bone marrow cells, used to help decide when to give next chemotherapy treatment. Chemotherapy hits both tumour cells and normal cells but bone marrow cells return to normal quicker than tumour cells - therefore want to give next dose of chemotherapy when bone marrow cells are normal but tumour cells are still low.

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2
Q

Name a cancer that is highly sensitive to chemotherapy, moderately sensitive and has low sensitivity.

A

Highly sensitive - lymphomas, neuroblastoma
Moderately sensitive - breast, cervical
Low sensitivity - prostate, renal cell

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3
Q

Name the 3 categories of chemotherapy drugs.

A

1) alkylating agents
2) antimetabolites
3) spindle poisons

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4
Q

Name an alkylating agent used for chemotherapy and its MOA of action.

A

Cisplatin (platinum compound)

Attaches an alkyl group to DNA, leads to DNA damage and inhibition of DNA synthesis.

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5
Q

Name 2 antimetabolites used for chemotherapy.

A

Methotrexate

5-fluorouracil

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6
Q

What is the mechanism of action of methotrexate when used for chemotherapy?

A

Inhibits dihydrofolate reductase (enzyme in folate pathway) - inhibits cell growth and division as you need folate to make purines.

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7
Q

What is 5-fluorouracil used for and what is its mechanism of action?

A

Chemotherapy
Inhibits thymidylate synthase enzyme (enzyme in folate pathway) - inhibits cell growth and division as folate is needed to produced purines.

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8
Q

Which DNA bases are purines and which are pyrimidines?

A

Purines (2 rings) - adenine, guanine

Pyrimidines (1 ring) - cytosine, thymine, uracil

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9
Q

Name the 2 types of spindle poisons used for chemotherapy and the mechanism of action of each.

A
  • vinca alkaloids e.g. Vincristine - inhibit microtubule assembly
  • taxanes e.g. Paclitaxel - inhibit microtubule polymerisation
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10
Q

What is the most common route of administration for chemotherapy?

A

IV - through a PICC line (in the arm) or Hickman line (in the chest).

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11
Q

Side effects of chemotherapy are very systemic (affect the whole body), why is this?

A

Because chemotherapy targets any organ system that has dividing cells.

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12
Q

What is the mechanism of action of spindle poisons in chemotherapy.

A

Inhibit normal microtubule function, interrupting mitosis.

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13
Q

How can chemotherapy lead to peritonitis?

A

If the tumour is in the GI tract, a hole can be left after the tumour dissolves, if food gets into the peritoneum through this hole then you can get peritonitis.

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14
Q

State the main side effects of chemotherapy.

A
  • renal failure
  • vomiting
  • alopecia
  • skin toxicity - local irritation or thrombophlebitis (clot formation in veins)
  • lung toxicity - pulmonary fibrosis
  • mucositis - sore mouth/thorat, diarrhoea, GI bleeds or oral thrush
  • myelosuppression
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15
Q

How can chemotherapy lead to renal failure?

A

Rapid tumour lysis leads to release of lots of toxins such as urea. Hyperuricaemia can lead to urate crystals forming in the kidneys, causing renal failure.

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16
Q

Name an infection that people having chemotherapy are particularly susceptible to.

A

Candida infections by Candida albicans.

17
Q

How might protein binding affect chemotherapy?

A

Low albumin/low protein binding can lead to toxicity due to increased free drug - therefore the dose needs to be reduced.

18
Q

Name 3 ways in which chemotherapy treatment is monitored.

A
  • response of cancer - radiological imaging, tumour marker blood tests
  • drug levels - measuring drug levels to ensure clearance from the body
  • checking for organ damage e.g. Measuring creatinine clearance
19
Q

Name 2 tumour markers for testicular cancer.

A

Alpha-fetoprotein

Beta hcg

20
Q

Name a tumour marker for prostate cancer.

A

Prostate specific antigen (PSA).

21
Q

Name a tumour marker for ovarian cancer.

A

Alpha-fetoprotein

22
Q

Name some tumour markers for breast cancer.

A

HER-2
Oestrogen receptors
Progesterone receptors