Althuis Michelle D, Scoccia Bert, Lamb Emmet J, Moghissi Kamran S, Westhoff Carolyn L, Mabie Jerome E, Brinton Louise A
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Am J Obstet Gynecol. 2005 Sep;193(3 Pt 1):668-74. doi: 10.1016/j.ajog.2005.01.091.
This study was undertaken to evaluate melanoma, thyroid, colon, and cervical cancer risks after clomiphene or gonadotropins.
Retrospective cohort of 8422 women (155,527 women-years) evaluated for infertility (1965-1988). Through 1999, cancers were ascertained by questionnaire, cancer and death registries. Poisson regression estimated adjusted rate ratios (RRs).
Clomiphene use did not significantly increase risk of melanoma (RR=1.66; 95% CI, 0.9-3.1), thyroid (RR=1.42; 95% CI, 0.5-3.7), cervical (RR=1.61; 95% CI, 0.5-4.7), or colon cancer (RR=0.83; 95% CI, 0.4-1.9). We found no relationship between clomiphene dose or cycles of use and cancer risk at any site. Clomiphene use may impart stronger effects on risks of melanoma (RR=2.00; 95% CI, 0.9-4.6) and thyroid cancer among women who remained nulliparous (RR=4.23; 95% CI, 1.0-17.1). Gonadotropins did not increase cancer risk for these sites.
Fertility drugs do not appear to have strong effects on these cancers. Nonetheless, follow-up should be pursued to assess long-term risks and to monitor effects among women who remain nulliparous.
本研究旨在评估克罗米芬或促性腺激素治疗后发生黑色素瘤、甲状腺癌、结肠癌和宫颈癌的风险。
对8422名女性(155,527人年)进行回顾性队列研究,这些女性在1965年至1988年期间因不孕症接受评估。截至1999年,通过问卷调查、癌症和死亡登记处确定癌症情况。采用泊松回归估计调整后的率比(RRs)。
使用克罗米芬并未显著增加黑色素瘤(RR = 1.66;95%可信区间[CI],0.9 - 3.1)、甲状腺癌(RR = 1.42;95% CI,0.5 - 3.7)、宫颈癌(RR = 1.61;95% CI,0.5 - 4.7)或结肠癌(RR = 0.83;95% CI,0.4 - 1.9)的风险。我们发现克罗米芬的剂量或使用周期与任何部位的癌症风险之间均无关联。在未生育的女性中,使用克罗米芬可能对黑色素瘤(RR = 2.00;95% CI,0.9 - 4.6)和甲状腺癌风险产生更强的影响(RR = 4.23;95% CI,1.0 - 17.1)。促性腺激素并未增加这些部位的癌症风险。
生育药物似乎对这些癌症没有强烈影响。尽管如此,仍应进行随访以评估长期风险,并监测未生育女性中的影响。