Department of Obstetrics and Gynaecology, Helsinki University Central Hospital, PO Box 140, FI-00029 HUS, Finland.
Gynecol Oncol. 2012 Aug;126(2):241-4. doi: 10.1016/j.ygyno.2012.04.045. Epub 2012 May 2.
Primary fallopian tube carcinoma (PFTC) is a rare malignancy and only sparse data exist on its possible association with postmenopausal hormone therapy (HT). We therefore studied this association in a nationwide cohort of Finnish HT users.
All women> 50 years using systemic estradiol-only therapy (ET) (n=117,820 hysterectomized women) or estradiol-progestin therapy (EPT) (n=247,781 nonhysterectomized women) for ≥ 6 months during 1994-2008 were identified from the national medical reimbursement register. The incidence of PFTC in HT users was compared to that in the comparable background population (standardized incidence ratio, SIR, with 95% confidence interval, CI).
A total of 160 cases of PFTC were encountered in users of ET (n=34) or EPT (n=126). The use of EPT ≥ 5 years was accompanied by an increased risk for PFTC (SIR 2.15; 95% CI 1.66-2.72). The SIR increased further to 3.36 (95% CI 2.02-5.24) when EPT use lasted ≥ 10 years. The EPT-related risk for PFTC was restricted to the sequential EPT and it was not seen for continuous EPT. Two leading progestins in EPT, norethisterone acetate and medroxyprogesterone acetate, associated with comparable risk elevations. ET use was not associated with the risk for PFTC.
The long-term, sequential use of EPT associates with an increased risk for PFTC. In absolute terms, 4 additional cases of PFTC would be detected in 10-year follow-up of 10,000 women who have used EPT for at least 5 years.
原发性输卵管癌(PFTC)是一种罕见的恶性肿瘤,关于其与绝经后激素治疗(HT)的可能关联仅有少量数据。因此,我们在芬兰 HT 使用者的全国性队列中研究了这种关联。
从国家医疗报销登记处确定了所有在 1994 年至 2008 年期间使用系统雌激素(ET)(n=117820 例子宫切除术妇女)或雌孕激素(EPT)(n=247781 例非子宫切除术妇女)治疗至少 6 个月的> 50 岁女性。将 HT 使用者中 PFTC 的发生率与可比背景人群(标准化发病率比[SIR],95%置信区间[CI])进行比较。
在 ET(n=34)或 EPT(n=126)使用者中共发现 160 例 PFTC 病例。EPT 使用≥ 5 年与 PFTC 风险增加相关(SIR 2.15;95%CI 1.66-2.72)。当 EPT 使用时间≥ 10 年时,SIR 进一步增加至 3.36(95%CI 2.02-5.24)。EPT 相关的 PFTC 风险仅限于序贯 EPT,而连续 EPT 则没有这种风险。EPT 中两种主要孕激素醋酸炔诺酮和醋酸甲地孕酮与相当的风险升高相关。ET 使用与 PFTC 风险无关。
长期序贯使用 EPT 与 PFTC 风险增加相关。在绝对意义上,在 10,000 名至少使用 5 年 EPT 的女性的 10 年随访中,将额外发现 4 例 PFTC 病例。