Department of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
JAMA Netw Open. 2024 Aug 1;7(8):e2429772. doi: 10.1001/jamanetworkopen.2024.29772.
The standard adjuvant treatment for patients with ERRB2-positive breast cancer is chemotherapy plus 1 year of trastuzumab. Shorter durations of trastuzumab administration improve cardiac safety, but more information is needed about their effect on survival.
To compare survival outcomes after 9-week vs 1-year administration of trastuzumab with the same adjuvant chemotherapy.
DESIGN, SETTING, AND PARTICIPANTS: This post hoc secondary analysis of an open-label, multicenter, noninferiority-design randomized clinical trial included women aged 18 years or older with early ERBB2-positive, axillary node-negative or axillary node-positive breast cancer who were enrolled from January 3, 2008, to December 16, 2014, at 65 centers in 7 European countries. The current exploratory analysis was conducted after achieving the maximum attainable follow-up data when the last patient enrolled had completed the last scheduled visit in December 2022.
Chemotherapy consisted of 3 cycles of docetaxel administered at 3-week intervals followed by 3 cycles of fluorouracil, epirubicin, and cyclophosphamide at 3-week intervals. Trastuzumab was administered in both groups for 9 weeks concomitantly with docetaxel. In the 9-week group, no further trastuzumab was administered after chemotherapy, whereas in the 1-year group, trastuzumab was continued after chemotherapy to complete 1 year of administration.
The primary objective was disease-free survival (DFS). Distant DFS and OS were secondary objectives. Survival between groups was compared using the Kaplan-Meier method and log-rank test or univariable Cox proportional hazards regression.
Among the 2174 women analyzed, median age was 56 years (IQR, 48-64 years). The median follow-up time was 8.1 years (IQR, 8.0-8.9 years); 357 DFS events and 176 deaths occurred. Trastuzumab for 9 weeks was associated with shorter DFS compared with trastuzumab for 1 year (hazard ratio [HR], 1.36; 90% CI, 1.14-1.62); 10-year DFS was 80.3% in the 1-year group vs 78.6% in the 9-week group. The 5-year and 10-year OS rates were comparable between the 9-week and 1-year groups (95.0% vs 95.9% and 89.1% vs 88.2%, respectively; HR for all time points, 1.20; 90% CI, 0.94-1.54). In multivariable analyses, 9-week treatment was associated with shorter DFS compared with 1-year treatment (HR for recurrence or death, 1.36; 95% CI, 1.10-1.68; P = .005), but there was no between-group difference in OS (HR, 1.22; 95% CI, 0.90-1.64; P = .20). Only 4 patients (0.2%) died of a cardiac cause.
In this secondary analysis of a randomized clinical trial, 1-year vs 9-week adjuvant trastuzumab was associated with improved DFS among patients with ERRB2-positive breast cancer receiving chemotherapy, but there was no significant difference in OS between the groups.
ClinicalTrials.gov Identifier: NCT00593697.
重要性:对于 ERBB2 阳性乳腺癌患者,标准辅助治疗是化疗加 1 年曲妥珠单抗治疗。曲妥珠单抗给药时间缩短可改善心脏安全性,但关于其对生存的影响还需要更多的信息。
目的:比较接受相同辅助化疗的 9 周与 1 年曲妥珠单抗给药的生存结局。
设计、地点和参与者:这是一项多中心、开放性、非劣效性随机临床试验的事后二次分析,纳入了年龄在 18 岁及以上的早期 ERBB2 阳性、腋窝淋巴结阴性或腋窝淋巴结阳性乳腺癌患者,于 2008 年 1 月 3 日至 2014 年 12 月 16 日在 7 个欧洲国家的 65 个中心入组。目前的探索性分析是在最后一名入组患者完成 2022 年 12 月最后一次预定访视时达到最大可获得随访数据后进行的。
干预措施:化疗包括 3 个周期的多西他赛,每 3 周给药 1 次,随后是 3 个周期的氟尿嘧啶、表柔比星和环磷酰胺,每 3 周给药 1 次。在这两组中,曲妥珠单抗均与多西他赛同时给药 9 周。在 9 周组中,化疗后不再给予曲妥珠单抗,而在 1 年组中,化疗后继续给予曲妥珠单抗,完成 1 年的给药。
主要结果和测量:主要终点是无病生存(DFS)。远处 DFS 和 OS 是次要终点。使用 Kaplan-Meier 方法和对数秩检验或单变量 Cox 比例风险回归比较组间生存。
结果:在分析的 2174 名女性中,中位年龄为 56 岁(IQR,48-64 岁)。中位随访时间为 8.1 年(IQR,8.0-8.9 年);发生 357 例 DFS 事件和 176 例死亡。与 1 年曲妥珠单抗相比,9 周曲妥珠单抗与较短的 DFS 相关(风险比 [HR],1.36;90%CI,1.14-1.62);10 年 DFS 在 1 年组为 80.3%,在 9 周组为 78.6%。9 周和 1 年组的 5 年和 10 年 OS 率相当(5 年分别为 95.0% vs 95.9%和 89.1% vs 88.2%;所有时间点的 HR,1.20;90%CI,0.94-1.54)。多变量分析显示,与 1 年治疗相比,9 周治疗与较短的 DFS 相关(复发或死亡的 HR,1.36;95%CI,1.10-1.68;P = 0.005),但两组间 OS 无差异(HR,1.22;95%CI,0.90-1.64;P = 0.20)。仅 4 例(0.2%)患者因心脏原因死亡。
结论和相关性:在这项随机临床试验的二次分析中,与接受化疗的 ERBB2 阳性乳腺癌患者接受 1 年 vs 9 周辅助曲妥珠单抗治疗相比,DFS 得到改善,但两组间 OS 无显著差异。
试验注册:ClinicalTrials.gov 标识符:NCT00593697。