Effects of fertility drugs on cancers other than breast and gynecologic malignancies
Ovulation-stimulating drugs were unrelated to lung or colorectal cancer risks, but possibly related to slight risk increases for melanomas and thyroid cancers, supporting the need for further evaluation of these cancers.
Louise A. Brinton, Ph.D., Kamran S. Moghissi, M.D., Bert Scoccia, M.D., Emmet J. Lamb, M.D., Britton Trabert, Ph.D., Shelley Niwa, M.A., David Ruggieri, B.S., Carolyn L. Westhoff, M.D.
Volume 104, Issue 4, Pages 980-988
To examine the relationship of ovulation-stimulating drugs to risk of cancers other than breast and gynecologic malignancies.
Retrospective cohort study, with additional follow-up since initial report.
Five US reproductive endocrinology practices.
Among a cohort of 12,193 women evaluated for infertility between 1965 and 1988, a total of 9,892 women (81.1% of the eligible population) were followed through 2010, via passive and active (questionnaire) approaches.
Main Outcome Measure(s):
Hazard ratios (HRs) and 95% confidence intervals (CIs) for various fertility treatment parameters for select cancers.
During 30.0 median years of follow-up (285,332 person-years), 91 colorectal cancers, 84 lung cancers, 55 thyroid cancers, and 70 melanomas were diagnosed among study subjects. Clomiphene citrate (CC), used by 38.1% of patients, was not associated with colorectal or lung cancer risks, but was related significantly to melanoma (HR = 1.95; 95% CI: 1.18–3.22), and non-significantly to thyroid cancer risks (HR = 1.57; 95% CI: 0.89–2.75). The highest melanoma risks were seen among those with the lowest drug exposure levels, but thyroid cancer risk was greatest among the heavily exposed patients (HR = 1.96; 95% CI: 0.92–4.17) for those receiving >2,250 mg. Clomiphene citrate–associated risks for thyroid cancer were somewhat higher among nulligravid, compared with gravid, women, but did not differ according to distinct causes of infertility. Gonadotropins, used by only 9.7% of subjects, were not related to risk of any of the assessed cancers.
Our results provide support for continued monitoring of both melanoma and thyroid cancer risk among patients receiving fertility drugs.
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