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.
引用
收藏
页码:492 / 498
页数:7
相关论文
共 14 条
[11]   Dual Targeting of HER2-Positive Cancer with Trastuzumab Emtansine and Pertuzumab: Critical Role for Neuregulin Blockade in Antitumor Response to Combination Therapy [J].
Phillips, Gail D. Lewis ;
Fields, Carter T. ;
Li, Guangmin ;
Dowbenko, Donald ;
Schaefer, Gabriele ;
Miller, Kathy ;
Andre, Fabrice ;
Burris, Howard A., III ;
Albain, Kathy S. ;
Harbeck, Nadia ;
Dieras, Veronique ;
Crivellari, Diana ;
Fang, Liang ;
Guardino, Ellie ;
Olsen, Steven R. ;
Crocker, Lisa M. ;
Sliwkowski, Mark X. .
CLINICAL CANCER RESEARCH, 2014, 20 (02) :456-468
[12]   Pertuzumab, trastuzumab, and docetaxel for HER2-positive metastatic breast cancer (CLEOPATRA study): overall survival results from a randomised, double-blind, placebo-controlled, phase 3 study [J].
Swain, Sandra M. ;
Kim, Sung-Bae ;
Cortes, Javier ;
Ro, Jungsil ;
Semiglazov, Vladimir ;
Campone, Mario ;
Ciruelos, Eva ;
Ferrero, Jean-Marc ;
Schneeweiss, Andreas ;
Knott, Adam ;
Clark, Emma ;
Ross, Graham ;
Benyunes, Mark C. ;
Baselga, Jose .
LANCET ONCOLOGY, 2013, 14 (06) :461-471
[13]   Trastuzumab Emtansine for HER2-Positive Advanced Breast Cancer [J].
Verma, Sunil ;
Miles, David ;
Gianni, Luca ;
Krop, Ian E. ;
Welslau, Manfred ;
Baselga, Jose ;
Pegram, Mark ;
Oh, Do-Youn ;
Dieras, Veronique ;
Guardino, Ellie ;
Fang, Liang ;
Lu, Michael W. ;
Olsen, Steven ;
Blackwell, Kim .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (19) :1783-1791
[14]   A retrospective multicentric observational study of trastuzumab emtansine in HER2 positive metastatic breast cancer: a real-world experience [J].
Vici, Patrizia ;
Pizzuti, Laura ;
Michelotti, Andrea ;
Sperduti, Isabella ;
Natoli, Clara ;
Mentuccia, Lucia ;
Di Lauro, Luigi ;
Sergi, Domenico ;
Marchetti, Paolo ;
Santini, Daniele ;
Magnolfi, Emanuela ;
Iezzi, Laura ;
Moscetti, Luca ;
Fabbri, Agnese ;
Cassano, Alessandra ;
Grassadonia, Antonino ;
Omarini, Claudia ;
Piacentini, Federico ;
Botticelli, Andrea ;
Bertolini, Ilaria ;
Scinto, Angelo Fedele ;
Zampa, Germano ;
Mauri, Maria ;
D'Onofrio, Loretta ;
Sini, Valentina ;
Barba, Maddalena ;
Maugeri-Sacca, Marcello ;
Rossi, Ernesto ;
Landucci, Elisabetta ;
Tomao, Silverio ;
Alberti, Antonio Maria ;
Giotta, Francesco ;
Ficorella, Corrado ;
Adamo, Vincenzo ;
Russo, Antonio ;
Lorusso, Vito ;
Cannita, Katia ;
Barni, Sandro ;
Laudadio, Lucio ;
Greco, Filippo ;
Garrone, Ornella ;
Della Giulia, Marina ;
Marolla, Paolo ;
Sanguineti, Giuseppe ;
Di Cocco, Barbara ;
Ciliberto, Gennaro ;
De Maria, Ruggero ;
Gamucci, Teresa .
ONCOTARGET, 2017, 8 (34) :56921-56931