C. Lhomme et al., ARE THERE ANY ARGUMENTS TO PROSCRIBE HORM ONE REPLACEMENT THERAPY IN WOMEN TREATED FOR OVARIAN ADENOCARCINOMA, Bulletin du cancer, 84(10), 1997, pp. 981-986
The hormonal status of 95% of the women treated for epithelial ovarian
carcinoma is menopausal either naturally or after treatment This rais
es the important question of the hormonal replacement therapy (HRT) am
ong these patients. Several retrospective studies have explored the po
tentiel positive or negative influence of HRT on the genesis of ovaria
n adenocarcinoma. Although somehow contradictory, these studies taken
all together fail to show any favouring nor protective role of HRT. In
vitro, estrogens have been shown to induce the proliferation of ovari
an cancer cell lines. On the opposite, progesterone and antiestrogens
have antiproliferative effects. Both types of effects are mediated by
intracellular steroid hormone receptors (ER, PgR). Although high dose
progesterone derivatives and antiestrogens have been shown to obtain t
herapeutic responses in patients carrying advanced ovarian carcinoma,
response rates were usually less than 20%, and no clinico-biological c
orrelation (with ER, PgR status) could be demonstrated. There is there
fore no evidence for a clinical significance of the presence of hormon
al receptors in these tumors. A single retrospective study explored th
e possible influence of HRT on the prognosis of patients treated for o
varian carcinoma, and did not demonstrate any deleterious effect. This
review of recent epidemiological, biological and clinical data fails
to find any argument against the prescription of HRT in patients treat
ed for ovarian adenocarcinoma, in the absence of other contra-indicati
ons.