Comprehensive Cancer Center Vienna, Medical University of Vienna, Austria ; Department of Medicine 1, Clinical Division of Oncology, Medical University of Vienna, Austria.
Comprehensive Cancer Center Vienna, Medical University of Vienna, Austria ; Department of Pathology, Medical University of Vienna, Austria.
Breast Care (Basel). 2014 Oct;9(5):344-8. doi: 10.1159/000368330.
This retrospective analysis was planned as a direct comparison of taxanes plus trastuzumab to the less toxic combination of oral vinorelbine (OV) plus trastuzumab as a first-line therapy for metastatic HER2-positive breast cancer.
Patients (n = 76) receiving either taxanes (group A) or OV (group B) in combination with trastuzumab were identified from a breast cancer database. Progression-free survival (PFS) was defined as the primary study endpoint; secondary endpoints were overall survival (OS), response rate (RR), incidence of brain metastases, and brain metastases-free survival (BMFS).
36 patients received taxanes and 40 patients OV in combination with trastuzumab. At a median follow-up of 47.5 months, median PFS was 7 months (group A) and 9 months in group B (log-rank; non-significant), respective numbers for OS were 49 and 59 months (p = 0.033). The incidence of brain metastases did not differ significantly between the 2 treatment groups, whereas BMFS was significantly longer in patients receiving OV.
OV plus trastuzumab yielded similar results in terms of PFS and RR and was superior in terms of OS and BMFS. These results add to the growing body of evidence that vinorelbine is a viable alternative to taxanes in HER2-positive metastatic breast cancer.
本回顾性分析旨在直接比较紫杉烷类药物联合曲妥珠单抗与毒性较低的长春瑞滨(OV)联合曲妥珠单抗作为 HER2 阳性转移性乳腺癌一线治疗的方案。
从乳腺癌数据库中确定了接受紫杉烷类药物(A 组)或 OV(B 组)联合曲妥珠单抗治疗的患者。无进展生存期(PFS)被定义为主要研究终点;次要终点包括总生存期(OS)、缓解率(RR)、脑转移发生率和脑转移无进展生存期(BMFS)。
36 例患者接受紫杉烷类药物联合曲妥珠单抗治疗,40 例患者接受 OV 联合曲妥珠单抗治疗。中位随访 47.5 个月时,A 组的中位 PFS 为 7 个月,B 组为 9 个月(对数秩检验;无统计学意义),OS 的相应数字分别为 49 个月和 59 个月(p=0.033)。两组患者的脑转移发生率无显著差异,而接受 OV 治疗的患者 BMFS 显著延长。
OV 联合曲妥珠单抗在 PFS 和 RR 方面的结果相似,但在 OS 和 BMFS 方面具有优势。这些结果增加了越来越多的证据,表明长春瑞滨在 HER2 阳性转移性乳腺癌中是紫杉烷类药物的可行替代药物。