Swerdlow A J, Jones M E
Section of Epidemiology, Institute of Cancer Research, Sutton, Surrey, UK.
Br J Cancer. 2007 Mar 12;96(5):850-5. doi: 10.1038/sj.bjc.6603605. Epub 2007 Feb 6.
As tamoxifen stimulates ovarian steroidogenesis in premenopausal women, induces ovulation and increases the incidence of benign ovarian cysts, there has been concern that it might also increase ovarian cancer risk in women treated premenopausally. In a national case-control study in Britain, treatment histories were collected for 158 cases of ovarian cancer after breast cancer diagnosed at ages under 55 years and 464 controls who had breast cancer at these ages without subsequent ovarian cancer. Risk of ovarian cancer was not raised for women overall who had taken tamoxifen (odds ratio (OR)=0.9, 95% confidence interval (CI) 0.6-1.3) or for those treated when premenopausal (OR=1.0, 95% CI 0.6-1.6) or perimenopausal (OR=0.7, 95% CI 0.2-2.4). There was also no relation of risk to daily dose, duration or cumulative dose of tamoxifen, or time since last use. There was, however, a significantly raised risk in relation to non-hormonal chemotherapy. The results suggest that tamoxifen treatment of premenopausal or perimenopausal women does not materially affect ovarian cancer risk, but that non-hormonal chemotherapy might increase risk.
由于他莫昔芬可刺激绝经前女性的卵巢甾体激素生成,诱发排卵并增加良性卵巢囊肿的发生率,因此人们担心它可能也会增加绝经前接受治疗女性患卵巢癌的风险。在英国的一项全国性病例对照研究中,收集了158例55岁以下乳腺癌诊断后发生卵巢癌的病例以及464例这些年龄段患乳腺癌但随后未发生卵巢癌的对照的治疗史。总体而言,服用他莫昔芬的女性(比值比(OR)=0.9,95%置信区间(CI)0.6 - 1.3)、绝经前接受治疗的女性(OR=1.0,95%CI 0.6 - 1.6)或围绝经期接受治疗的女性(OR=0.7,95%CI 0.2 - 2.4)患卵巢癌的风险并未升高。风险与他莫昔芬的每日剂量、疗程或累积剂量,或末次使用后的时间也无关。然而,与非激素化疗相关的风险显著升高。结果表明,他莫昔芬治疗绝经前或围绝经期女性对卵巢癌风险没有实质性影响,但非激素化疗可能会增加风险。