Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Mailman School of Public Health, Columbia University, New York, New York.
JAMA Oncol. 2021 Apr 1;7(4):585-592. doi: 10.1001/jamaoncol.2020.7995.
Women with pathogenic variants in BRCA1 and BRCA2 are at high risk of developing breast and ovarian cancers. They usually undergo intensive cancer surveillance and may also consider surgical interventions, such as risk-reducing mastectomy or risk-reducing salpingo-oophorectomy (RRSO). Risk-reducing salpingo-oophorectomy has been shown to reduce ovarian cancer risk, but its association with breast cancer risk is less clear.
To assess the association of RRSO with the risk of breast cancer in women with BRCA1 and BRCA2 pathogenic variants.
DESIGN, SETTING, AND PARTICIPANTS: This case series included families enrolled in the Breast Cancer Family Registry between 1996 and 2000 that carried an inherited pathogenic variant in BRCA1 (498 families) or BRCA2 (378 families). A survival analysis approach was used that was designed specifically to assess the time-varying association of RRSO with breast cancer risk and accounting for other potential biases. Data were analyzed from August 2019 to November 2020.
Risk-reducing salpingo-oophorectomy.
In all analyses, the primary end point was the time to a first primary breast cancer.
A total of 876 families were evaluated, including 498 with BRCA1 (2650 individuals; mean [SD] event age, 55.8 [19.1] years; 437 White probands [87.8%]) and 378 with BRCA2 (1925 individuals; mean [SD] event age, 57.0 [18.6] years; 299 White probands [79.1%]). Risk-reducing salpingo-oophorectomy was associated with a reduced risk of breast cancer for BRCA1 and BRCA2 pathogenic variant carriers within 5 years after surgery (hazard ratios [HRs], 0.28 [95% CI, 0.10-0.63] and 0.19 [95% CI, 0.06-0.71], respectively), whereas the corresponding HRs were weaker after 5 years postsurgery (HRs, 0.64 [95% CI, 0.38-0.97] and 0.99 [95% CI; 0.84-1.00], respectively). For BRCA1 and BRCA2 pathogenic variant carriers who underwent RRSO at age 40 years, the cause-specific cumulative risk of breast cancer was 49.7% (95% CI, 40.0-60.3) and 52.7% (95% CI, 47.9-58.7) by age 70 years, respectively, compared with 61.0% (95% CI, 56.7-66.0) and 54.0% (95% CI, 49.3-60.1), respectively, for women without RRSO.
Although the primary indication for RRSO is the prevention of ovarian cancer, it is also critical to assess its association with breast cancer risk in order to guide clinical decision-making about RRSO use and timing. The results of this case series suggest a reduced risk of breast cancer associated with RRSO in the immediate 5 years after surgery in women carrying BRCA1 and BRCA2 pathogenic variants, and a longer-term association with cumulative breast cancer risk in women carrying BRCA1 pathogenic variants.
重要性:携带 BRCA1 和 BRCA2 种系致病性变异的女性发生乳腺癌和卵巢癌的风险很高。她们通常会接受密集的癌症监测,也可能考虑进行手术干预,如降低风险的乳房切除术或降低风险的输卵管卵巢切除术(RRSO)。已经证明降低风险的输卵管卵巢切除术可以降低卵巢癌的风险,但它与乳腺癌风险的关联不太清楚。
目的:评估 RRSO 与携带 BRCA1 和 BRCA2 种系致病性变异的女性乳腺癌风险的相关性。
设计、地点和参与者:本病例系列研究纳入了 1996 年至 2000 年间参加乳腺癌家族登记处的家族,这些家族携带 BRCA1(498 个家族)或 BRCA2(378 个家族)的遗传性致病性变异。采用了一种专门设计的生存分析方法,旨在评估 RRSO 与乳腺癌风险的时间变化相关性,并考虑其他潜在的偏倚。数据的分析时间是从 2019 年 8 月到 2020 年 11 月。
暴露:降低风险的输卵管卵巢切除术。
主要结局和测量:在所有分析中,主要终点是首次原发性乳腺癌的发病时间。
结果:共评估了 876 个家族,其中 498 个家族携带 BRCA1(2650 人;平均[标准差]发病年龄,55.8[19.1]岁;437 名白人先证者[87.8%]),378 个家族携带 BRCA2(1925 人;平均[标准差]发病年龄,57.0[18.6]岁;299 名白人先证者[79.1%])。RRSO 后 5 年内,BRCA1 和 BRCA2 种系致病性变异携带者的乳腺癌风险降低(风险比[HR],0.28[95%CI,0.10-0.63]和 0.19[95%CI,0.06-0.71]),而术后 5 年以上的 HR 较弱(HR,0.64[95%CI,0.38-0.97]和 0.99[95%CI,0.84-1.00])。对于在 40 岁时接受 RRSO 的 BRCA1 和 BRCA2 种系致病性变异携带者,乳腺癌的特定病因累积风险分别为 49.7%(95%CI,40.0-60.3)和 52.7%(95%CI,47.9-58.7),而未接受 RRSO 的女性分别为 61.0%(95%CI,56.7-66.0)和 54.0%(95%CI,49.3-60.1)。
结论和相关性:虽然 RRSO 的主要适应证是预防卵巢癌,但评估其与乳腺癌风险的相关性对于指导 RRSO 使用和时机的临床决策也至关重要。本病例系列研究的结果表明,BRCA1 和 BRCA2 种系致病性变异携带者在 RRSO 后 5 年内乳腺癌风险降低,而在携带 BRCA1 种系致病性变异的女性中,与乳腺癌累积风险的长期相关性。