Beth Israel Deaconess Medical Center, Boston, MA.
Mayo Clinic, Rochester, MN.
J Clin Oncol. 2020 Jun 20;38(18):2080-2106. doi: 10.1200/JCO.20.00299. Epub 2020 Apr 3.
To develop recommendations for management of patients with breast cancer (BC) with germline mutations in BC susceptibility genes.
The American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology convened an Expert Panel to develop recommendations based on a systematic review of the literature and a formal consensus process.
Fifty-eight articles met eligibility criteria and formed the evidentiary basis for the local therapy recommendations; six randomized controlled trials of systemic therapy met eligibility criteria.
Patients with newly diagnosed BC and / mutations may be considered for breast-conserving therapy (BCT), with local control of the index cancer similar to that of noncarriers. The significant risk of a contralateral BC (CBC), especially in young women, and the higher risk of new cancers in the ipsilateral breast warrant discussion of bilateral mastectomy. Patients with mutations in moderate-risk genes should be offered BCT. For women with mutations in / or moderate-penetrance genes who are eligible for mastectomy, nipple-sparing mastectomy is a reasonable approach. There is no evidence of increased toxicity or CBC events from radiation exposure in / carriers. Radiation therapy should not be withheld in carriers. For patients with germline mutations, mastectomy is advised; radiation therapy is contraindicated except in those with significant risk of locoregional recurrence. Platinum agents are recommended versus taxanes to treat advanced BC in carriers. In the adjuvant/neoadjuvant setting, data do not support the routine addition of platinum to anthracycline- and taxane-based chemotherapy. Poly (ADP-ribose) polymerase (PARP) inhibitors (olaparib and talazoparib) are preferable to nonplatinum single-agent chemotherapy for treatment of advanced BC in / carriers. Data are insufficient to recommend PARP inhibitor use in the early setting or in moderate-penetrance carriers. Additional information available at www.asco.org/breast-cancer-guidelines.
制定管理携带乳腺癌易感基因种系突变的乳腺癌患者的建议。
美国临床肿瘤学会、美国放射肿瘤学会和外科肿瘤学会召集专家小组,根据文献系统评价和正式共识过程制定建议。
符合条件的 58 篇文章为局部治疗建议提供了证据基础;符合条件的 6 项系统治疗随机对照试验。
新诊断为乳腺癌且携带 或 突变的患者可考虑保乳治疗(BCT),索引癌的局部控制与非携带者相似。对侧乳腺癌(CBC)的风险显著增加,尤其是年轻女性,以及同侧乳房新发癌症的风险较高,需要讨论双侧乳房切除术。携带中度风险基因的突变患者应提供 BCT。对于有 或中度外显率基因突变且有乳房切除术资格的女性,保留乳头的乳房切除术是一种合理的方法。携带 突变的患者没有辐射暴露增加毒性或 CBC 事件的证据。不应拒绝对 携带者进行放射治疗。对于携带种系 突变的患者,建议行乳房切除术;除局部区域复发风险显著增加的患者外,不建议进行放射治疗。铂类药物推荐用于治疗 携带者的晚期乳腺癌,优于紫杉烷类药物。在辅助/新辅助治疗中,数据不支持常规将铂类药物添加到蒽环类和紫杉烷类化疗中。聚(ADP-核糖)聚合酶(PARP)抑制剂(奥拉帕尼和他拉唑帕尼)是治疗 携带者晚期乳腺癌的首选药物,优于非铂类单药化疗。数据不足以推荐在早期或中度外显率携带者中使用 PARP 抑制剂。更多信息可在 www.asco.org/breast-cancer-guidelines 上获取。