Institut Curie, Department of Genetics, PSL Research University, Paris, France.
CHU, Department of Genetics, Lille, France.
Eur J Hum Genet. 2022 Sep;30(9):1060-1066. doi: 10.1038/s41431-022-01049-2. Epub 2022 Feb 25.
Women with pathogenic germline BRCA1 or BRCA2 variants have a higher risk of breast cancer than in the general population. International guidelines recommend specific clinical and radiological breast follow-up. This specific breast screening program has already been shown to be of clinical benefit, but no information is available concerning the use of prognostic factors or specific survival to guide follow-up decisions. We evaluated "high-risk" screening in a retrospective single-center study of 520 women carrying pathogenic germline variants of the BRCA1 or BRCA2 gene treated for breast cancer between January 2000 and December 2016. We compared two groups of women: the incidental breast cancer group (IBCG) were followed before breast cancer diagnosis (N = 103), whereas the prevalent breast cancer group (PBCG) (N = 417) had no specific follow-up for high risk before breast cancer diagnosis. Breast cancers were diagnosed at an earlier stage in the IBCG than in the PBCG: T0 in 64% versus 19% of tumors, (p < 0.00001), and N0 in 90% vs. 75% (p < 0.00001), respectively. Treatment differed significantly between the 2 groups: less neoadjuvant chemotherapy (7.1% vs. 28.5%, p < 0.00001), adjuvant chemotherapy (47.7% vs. 61.9%, p = 0.004) and more mastectomies (60% vs. 42% p < 0.0001) in the IBCG vs PBCG groups respectively. Overall and breast cancer-specific mortality were similar between the two groups. However, the patients in the IBCG had a significantly longer metastasis-free survival than those in the PBCG, at three years (96.9% [95% CI 93.5-100] vs. 92.30% [95% CI 89.8-94.9]; p = 0.02), suggesting a possible long-term survival advantage.
携带致病性 BRCA1 或 BRCA2 种系变异的女性患乳腺癌的风险高于普通人群。国际指南建议进行特定的临床和放射学乳房随访。已经证明这种特定的乳腺癌筛查方案具有临床益处,但尚无关于使用预后因素或特定生存指导随访决策的信息。我们评估了 2000 年 1 月至 2016 年 12 月期间接受乳腺癌治疗的 520 名携带 BRCA1 或 BRCA2 种系致病性变异的女性的回顾性单中心研究中的“高危”筛查。我们比较了两组女性:偶然发现乳腺癌组(IBCG)在乳腺癌诊断前接受随访(n=103),而在乳腺癌诊断前无高危因素特定随访的常见乳腺癌组(PBCG)(n=417)。IBCG 中的乳腺癌诊断分期更早:T0 期占 64%,而 PBCG 中 T0 期占 19%(p<0.00001),N0 期分别为 90%和 75%(p<0.00001)。两组之间的治疗差异显著:IBCG 中接受新辅助化疗的比例较低(7.1% vs. 28.5%,p<0.00001),辅助化疗(47.7% vs. 61.9%,p=0.004)和更多的乳房切除术(60% vs. 42%,p<0.0001)。两组的总生存率和乳腺癌特异性生存率相似。然而,IBCG 患者的无转移生存率明显长于 PBCG 患者,三年时分别为 96.9%(95%CI 93.5-100)和 92.30%(95%CI 89.8-94.9);p=0.02),表明可能有长期生存优势。