Hôpital Jean-Minjoz, Centre Hospitalier Universitaire INSERM 1098, Boulevard Fleming, 25030 Besançon, France.
Georges-François Leclerc, 1 Rue du Professeur Marion, 21000 Dijon, France.
Eur J Cancer. 2017 Aug;81:151-160. doi: 10.1016/j.ejca.2017.05.020. Epub 2017 Jun 16.
Adjuvant clinical trials in early human epidermal growth factor receptor 2 (HER2)-positive breast cancer have assessed either sequential or concomitant incorporation of trastuzumab with chemotherapy; only the North Central Cancer Treatment Group (NCCTG)-N9831 trial prospectively compared both modalities. In routine trastuzumab has been incorporated into a concurrent regimen with taxane chemotherapy instead of sequential modality on the basis of a positive risk-benefit ratio. This present study assessed sequential versus concomitant administration of adjuvant trastuzumab.
A population combining patients from Protocol for Herceptin as Adjuvant therapy with Reduced Exposure (PHARE) a randomised phase III clinical trial (NCT00381901) and SIGNAL (RECF1098) a prospective study specifically designed for Genome-wide Association Studies (GWAS) analyses was studied. In this cohort with 58 months of median follow-up, the comparison in the HER2-positive group of adjuvant trastuzumab and chemotherapy modalities was based on a propensity score methodology. Treatment modalities were based on physician's choice and comparisons adjustment were made by a propensity score methodology. Overall Survival (OS) and Disease-Free Survival (DFS) were estimated using the Kaplan-Meier method, and comparisons between groups were based on the log rank test.
The SIGNAL/PHARE cohort included 11,728 breast cancer cases treated in adjuvant setting; some 5502 of them with HER2-positive tumour: 34.5% (1897/5502) were treated by sequential and 65.5% (3605/5502) by concomitant modality of administration for taxane-chemotherapy and trastuzumab. The adjusted comparison found similar OS (HR = 1.01; 95% CI: 0.86-1.19) and similar DFS (HR = 1.08; 95% CI: 0.96-1.21).
These results suggest that the sequential administration of trastuzumab given after the completion of adjuvant chemotherapy might be as valid as the concomitant administration of trastuzumab and taxane chemotherapy in the adjuvant setting.
早期人类表皮生长因子受体 2(HER2)阳性乳腺癌的辅助临床试验评估了曲妥珠单抗与化疗的序贯或同时应用;只有北中央癌症治疗组(NCCTG)-N9831 试验前瞻性地比较了这两种方法。在常规治疗中,基于阳性风险效益比,曲妥珠单抗已与紫杉烷化疗同时应用,而不是序贯应用。本研究评估了辅助曲妥珠单抗的序贯与同时给药。
对来自 Herceptin 作为辅助治疗与减少暴露的协议(PHARE)的患者进行了人群研究,这是一项随机 III 期临床试验(NCT00381901),以及 SIGNAL(RECF1098),这是一项专门设计用于全基因组关联研究(GWAS)分析的前瞻性研究。在这项中位随访时间为 58 个月的队列研究中,基于倾向评分方法比较了 HER2 阳性组中辅助曲妥珠单抗和化疗方案的效果。治疗方案基于医生的选择,通过倾向评分方法进行调整。使用 Kaplan-Meier 方法估计总生存(OS)和无病生存(DFS),并通过对数秩检验比较组间差异。
SIGNAL/PHARE 队列包括 11728 例接受辅助治疗的乳腺癌病例;其中 5502 例为 HER2 阳性肿瘤:34.5%(1897/5502)接受序贯治疗,65.5%(3605/5502)接受同时治疗,即紫杉烷化疗和曲妥珠单抗。调整后的比较发现,OS 相似(HR=1.01;95%CI:0.86-1.19),DFS 相似(HR=1.08;95%CI:0.96-1.21)。
这些结果表明,辅助化疗完成后给予曲妥珠单抗的序贯给药与辅助治疗中曲妥珠单抗和紫杉烷化疗的同时给药一样有效。