Blue Book: Hormone Therapy for Cancer Flashcards

1
Q

When can hormone therapy be used?

A

For ‘hormone-dependent’ cancers: rate of growth is influenced by levels of hormones, interfering with those hormones may lead to growth arrest and tumour regression.

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2
Q

Which cancers are hormone sensitive?

A
Hormonal tissue cancers:
Sex hormones:
Prostate
Breast
Endometrium
Corticosteroids:
Lymphocytic Malignancies (lymphoma, leukaemia and myeloma:
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3
Q

When can hormonal treatment be used?

A

Neo-Adjuvant (shrink primary)
Instead of surgery (primary)
Prevent/delay growth of micro mets after surgery (adjacent)
Shrink established mets (palliative)

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4
Q

How can you remove the source of growth-promoting hormone?

A

Bilateral oophorectomy in pre-menopausal women/ bilateral orchidectomy in men. Remove sex hormones.

Permanent ovarian ablation induced by radiotherapy.

Medical castration: long-acting LHRH analogues. (goserelin): down regulate pituitary block LH and FSH production. This is not suitable in postmenopausal women as sex hormone is mainly extra-gonadal in fat and adrenals.

Aromatase inhibitors (prevent rate limiting step in oestrogen production) in post menopausal women occurs in fat/liver: anastrozole/exemestane/letrozole

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5
Q

Function and examples of hormone inhibitors.

1 x female
2 x male

A

Block binding of hormones to tumour cell.
Eg Tamoxifen anti-oestrogen

Anti-androgens:

  1. Steroidal ant-androgens: cyproterone acetate
    - inhibit androgen receptor and substitute testosterone in hypothalamus= negative feedback
  2. Non-steroidal anti-androgens: bicalutamide
    - inhibit testosterone in tumour cells and hypothalamus (causes rise in serum test) = give LHRH analogue
    - used in prostate cancer
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6
Q

When is increasing hormones level helpful?

3 scenarios.

A

Glucocorticoids in high concentrations induce apoptosis in malignant lymphoid cells.

Hormone supplementation in some sex-sensitive cancers to induce negative feedback loop.

Progestogens: orally high dose in progesterone sensitive tissues (breast & endometrium). Inhibit tumour growth by binding to PR and also produce negative feedback on pituitary/gonadal axis.

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