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曲妥珠单抗辅助治疗 ERBB2 阳性乳腺癌 9 周或 1 年的长期疗效:一项 SOLD 随机临床试验的二次分析。

Long-Term Outcomes of Adjuvant Trastuzumab for 9 Weeks or 1 Year for ERBB2-Positive Breast Cancer: A Secondary Analysis of the SOLD Randomized Clinical Trial.

机构信息

Department of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

出版信息

JAMA Netw Open. 2024 Aug 1;7(8):e2429772. doi: 10.1001/jamanetworkopen.2024.29772.

Abstract

IMPORTANCE

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.

OBJECTIVE

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.

INTERVENTION

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.

MAIN OUTCOMES AND MEASURES

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.

RESULTS

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.

CONCLUSIONS AND RELEVANCE

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.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT00593697.

摘要

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。

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