Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan.
Eastern Hepatobiliary Surgery Hospital, Second Military Medical University.
Medicine (Baltimore). 2021 Mar 12;100(10):e24995. doi: 10.1097/MD.0000000000024995.
Adjuvant trastuzumab improves survival outcomes of human epidermal receptor 2 positive early breast cancer patients. Currently, administration of 12 months adjuvant trastuzumab is the standard therapy. However, whether 6 months treatment is non-inferior to the standard 12 months treatment remains controversial.
Relevant records were searched in PubMed, Cochrane Library, Web of Science, and EMBASE through Jan 14, 2020. Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) for disease-free survival (DFS) and overall survival (OS) were meta-analyzed. The primary endpoint was DFS with a non-inferiority hazard margin of 1.2 and the second was OS with 1.43.
Three randomized clinical studies met the inclusion criteria, including 3974 patients in 6 months group and 3976 in 12 months group. HR for DFS was 1.18 (95% CI 0.97-1.44, P = .09), with the non-inferiority margin comprised in the 95% CI. HR for OS was 1.14 (95% CI 0.98-1.32, P= .08), whereas the upper limit of 95% CI did not exceed the non-inferiority hazard margin.
Our analysis failed to show that 6 months treatment was non-inferior to 12 months treatment in improving the DFS. Although the non-inferiority of the 6-month adjuvant trastuzumab treatment was found for OS, considering that breast cancer patients should receive additional systematic therapies when disease progression or relapse happens, we suggest that 12 months adjuvant trastuzumab treatment should remain the standard therapeutic strategy for patients with early human epidermal receptor 2 positive breast cancer.
曲妥珠单抗辅助治疗可改善人表皮生长因子受体 2 阳性早期乳腺癌患者的生存结局。目前,曲妥珠单抗辅助治疗 12 个月是标准治疗。然而,6 个月治疗是否不劣于标准 12 个月治疗仍存在争议。
检索 2020 年 1 月 14 日前 PubMed、Cochrane Library、Web of Science 和 EMBASE 中相关记录。采用荟萃分析评估无病生存(DFS)和总生存(OS)的风险比(HR)和 95%置信区间(CI)。主要终点为 DFS 非劣效性 HR 界值为 1.2,次要终点为 OS 的 HR 界值为 1.43。
纳入 3 项随机临床试验,6 个月组 3974 例,12 个月组 3976 例。DFS 的 HR 为 1.18(95% CI 0.97-1.44,P=0.09),非劣效性 HR 界值包含在 95% CI 内。OS 的 HR 为 1.14(95% CI 0.98-1.32,P=0.08),但 95% CI 的上限未超过非劣效性 HR 界值。
本分析结果未能表明 6 个月治疗在改善 DFS 方面不劣于 12 个月治疗。虽然 6 个月辅助曲妥珠单抗治疗在 OS 方面具有非劣效性,但考虑到乳腺癌患者在疾病进展或复发时需要接受额外的系统治疗,我们建议 12 个月曲妥珠单抗辅助治疗仍然是早期人表皮生长因子受体 2 阳性乳腺癌患者的标准治疗策略。