Rossing M A, Daling J R, Weiss N S, Moore D E, Self S G
Department of Epidemiology, School of Public Health and Community Medicine, University of Washington, Seattle.
N Engl J Med. 1994 Sep 22;331(12):771-6. doi: 10.1056/NEJM199409223311204.
Case reports and the results of a recent case-control study have raised questions about the potential neoplastic effects of medications used as treatment for infertility.
We examined the risk of ovarian tumors in a cohort of 3837 women evaluated for infertility between 1974 and 1985 in Seattle. Computer linkage with a population-based tumor registry was used to identify women in whom tumors were diagnosed before January 1, 1992. Data on infertility testing and treatment were abstracted from the medical records of women who had ovarian cancer and those of a randomly selected comparison group. The risk of ovarian tumors associated with exposure to ovulation-inducing medications was assessed through an age-standardized comparison with the rate of ovarian tumors in the general population, and Cox regression analysis was used to compare the risk of cancer among women who received these medications with the risk among infertile women who did not receive them.
There were 11 invasive or borderline malignant ovarian tumors, as compared with an expected number of 4.4 (standardized incidence ratio, 2.5; 95 percent confidence interval, 1.3 to 4.5). Nine of the women in whom ovarian tumors developed had taken clomiphene; the adjusted relative risk among these women, as compared with that among infertile women who had not taken this drug, was 2.3 (95 percent confidence interval, 0.5 to 11.4). Five of the nine women had taken the drug during 12 or more monthly cycles. This period of treatment was associated with an increased risk of ovarian tumors among both women with ovarian abnormalities and those without apparent abnormalities (relative risk, 11.1; 95 percent confidence interval, 1.5 to 82.3), whereas treatment with the drug for less than one year was not associated with an increased risk.
Prolonged use of clomiphene may increase the risk of a borderline or invasive ovarian tumor.
病例报告及近期一项病例对照研究的结果引发了关于用于治疗不孕症的药物潜在致癌作用的疑问。
我们调查了1974年至1985年在西雅图接受不孕症评估的3837名女性队列中卵巢肿瘤的风险。通过与基于人群的肿瘤登记处进行计算机链接,以识别在1992年1月1日前被诊断出患有肿瘤的女性。从患有卵巢癌的女性以及随机选择的对照组女性的病历中提取有关不孕症检查和治疗的数据。通过与一般人群中卵巢肿瘤发生率进行年龄标准化比较,评估与接触促排卵药物相关的卵巢肿瘤风险,并使用Cox回归分析比较接受这些药物治疗的女性患癌风险与未接受这些药物治疗的不孕女性患癌风险。
共有11例侵袭性或交界性恶性卵巢肿瘤,而预期数量为4.4例(标准化发病率比为2.5;95%置信区间为1.3至4.5)。发生卵巢肿瘤的9名女性服用过克罗米芬;与未服用此药的不孕女性相比,这些女性经调整后的相对风险为2.3(95%置信区间为0.5至11.4)。9名女性中有5名在12个或更多月经周期内服用过该药。这段治疗时间与卵巢异常女性和无明显异常女性的卵巢肿瘤风险增加相关(相对风险为11.1;95%置信区间为1.5至82.3),而用药少于一年与风险增加无关。
长期使用克罗米芬可能会增加交界性或侵袭性卵巢肿瘤的风险。