S. Barni et al., CLINICAL EFFICACY OF THE AROMATASE INHIBITOR ANASTROZOLE IN RELATION TO PROLACTIN SECRETION IN HEAVILY PRETREATED METASTATIC BREAST-CANCER, Tumori, 84(1), 1998, pp. 45-47
Aims and background: It is known that the aromatase inhibitors may act
by decreasing estrogen levels. Moreover, it is known that estrogens m
ay stimulate the release of prolactin (PRL), which is a growth factor
for breast cancer. This phase II study was performed to evaluate the e
ffects of the never aromatase inhibitor anastrozole on PRL secretion i
n metastatic breast cancer and the possible influence of PRL pretreatm
ent levels on the efficacy of therapy. Methods: The study involved 14
pretreated metastatic breast cancer patients with a poor clinical stat
us. Anastrozole was given orally once a day at 1 mg/day for at least 2
months. To evaluate PRL secretion, venous blood samples were collecte
d before treatment and at 1-monthly intervals during treatment. Result
s: The clinical response consisted of partial response (PR) in 2, stab
le disease (SD) in 5 and progressive disease (PD) in the remaining 7 p
atients. Abnormally high pretreatment levers of PRL were seen in 5/14
(36%) patients. Progressing patients showed significantly higher pretr
eatment levels of PRL than those who achieved PR or SD. None of the pa
tients with high PRL pretreatment levers showed a decline in PRL lever
s on treatment with anastrozole. Conclusions: This preliminary study s
uggests that anastrotole has no inhibitory effect on PRL secretion in
metastatic breast cancer and that the evidence of abnormally elevated
concentrations of PRL prior to therapy is generally associated with a
lack of efficacy.