Comparison of the efficacy of trastuzumab emtansine between patients with metastatic human epidermal growth factor receptor 2-positive breast cancers previously treated with combination trastuzumab and pertuzumab and with trastuzumab only in Japanese population

被引:19
作者
Noda-Narita, Shoko [1 ]
Shimomura, Akihiko [1 ]
Kawachi, Asuka [1 ]
Sumiyoshi-Okuma, Hitomi [1 ]
Sudo, Kazuki [1 ]
Shimoi, Tatsunori [1 ]
Noguchi, Emi [1 ]
Yonemori, Kan [1 ]
Shimizu, Chikako [1 ,2 ]
Fujiwara, Yasuhiro [1 ]
Tamura, Kenji [1 ]
机构
[1] Natl Canc Ctr, Dept Breast & Med Oncol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Natl Ctr Global Hlth & Med, Dept Breast Med Oncol, Shinjuku Ku, 1-21-1 Toyama, Tokyo 1628655, Japan
关键词
Trastuzumab emtansine; Metastatic breast cancer; Human epidermal growth factor 2; Trastuzumab; Pertuzumab; OPEN-LABEL; PHYSICIANS CHOICE; RESISTANCE; DOCETAXEL; TH3RESA;
D O I
10.1007/s12282-019-00949-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundTrastuzumab emtansine (T-DM1) has been approved since 2013 for patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC) who had received trastuzumab (Tmab) and taxane. However, no clinical trial has evaluated the efficacy of T-DM1 in those who have previously received pertuzumab (Pmab). This study aimed to compare the efficacy of T-DM1 between patients who had received Tmab and Pmab and those who hadreceived Tmab only in Japanese population.MethodsWe identified all patients with HER2-positive MBC who received T-DM1 between April 1, 2014 and February 28, 2017 in our institution. The patients were divided into the Tmab group (i.e., those who received only Tmab before T-DM1 treatment) and the Tmab/Pmab group (i.e., those who received Tmab and Pmab before T-DM1 treatment), and progression-free survival (PFS) and best response were compared between the two groups.ResultsA total of 42 patients were enrolled for outcome analysis. The median follow-up period was 4.8 months, and the median number of prior chemotherapy regimens for metastatic disease before T-DM1 was 1 (range 1-2) in the Tmab/Pmab group and 2 (range 0-6) in the Tmab group. The median PFS was 2.8 months in the Tmab/Pmab group (95% confidence interval [CI] 1.7-4.8 months) and 7.8 months in the Tmab group (95% CI 5.5-15.9 months) (p=0.0030). The best response was lower in the Tmab/Pmab group (11.1% vs. 25.0%).ConclusionsPatients with HER2-positive MBC who received Tmab and Pmab treatment before T-DM1 have fewer benefits from T-DM1.
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收藏
页码:492 / 498
页数:7
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