Capecitabine in Addition to Anthracycline- and Taxane-Based Neoadjuvant Treatment in Patients With Primary Breast Cancer: Phase III GeparQuattro Study

被引:176
|
作者
von Minckwitz, Gunter
Rezai, Mahdi
Loibl, Sibylle
Fasching, Peter A.
Huober, Jens
Tesch, Hans
Bauerfeind, Ingo
Hilfrich, Joern
Eidtmann, Holger
Gerber, Bernd
Hanusch, Claus
Kuehn, Thorsten
du Bois, Andreas
Blohmer, Jens-Uwe
Thomssen, Christoph
Costa, Serban Dan
Jackisch, Christian
Kaufmann, Manfred
Mehta, Keyur
Untch, Michael
机构
[1] German Breast Grp, Neu Isenburg, Germany
[2] Luisenkrankenhaus, Dusseldorf, Germany
[3] Onkol Bethanien, Frankfurt, Germany
[4] Univ Klinikums, Frauenklin, Erlangen, Germany
[5] Univ Tubingen Hosp, Tubingen, Germany
[6] Univ Munich, Klinikum Grosshadern, D-8000 Munich, Germany
[7] Klinikum Zum Roten Kreuz, Munich, Germany
[8] Frauenklin Henriettenstiftung, Hannover, Germany
[9] Univ Frauenklin, Kiel, Germany
[10] Univ Frauenklin, Rostock, Germany
[11] Frauenklinikum Gifhorn, Wiesbaden, Germany
[12] Dr Horst Schmidt Klin, Wiesbaden, Germany
[13] St Gertrauden Hosp, Berlin, Germany
[14] Univ Frauenklin, Halle, Germany
[15] Univ Frauenklin, Magdeburg, Germany
[16] HELIOS Klin, Berlin, Germany
关键词
RANDOMIZED GEPARTRIO; PLUS DOCETAXEL; TRIAL; CYCLOPHOSPHAMIDE; DOXORUBICIN; CHEMOTHERAPY; SURVIVAL;
D O I
10.1200/JCO.2009.23.8303
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Capecitabine can be integrated either concomitantly or sequentially to anthracycline-plus-taxane-based regimens. Patients and Methods Patients with large operable or locally advanced tumors, with hormone receptor-negative tumors, or with receptor-positive tumors but also clinically node-positive disease were recruited to receive preoperatively four cycles of epirubicin plus cyclophosphamide (EC; epirubicin 90 mg/m(2) and cyclophosphamide 600 mg/m(2)). Patients were then randomly assigned to four cycles of docetaxel (100 mg/m(2)), four cycles of docetaxel + capecitabine (TX; docetaxel 75 mg/m(2) plus capecitabine 1,800 mg/m(2)), or four cycles of docetaxel (75 mg/m(2)) followed by four cycles of capecitabine (1,800 mg/m(2); T-X). Patients with human epidermal growth factor receptor 2 (HER-2)-positive tumors received trastuzumab concomitantly with all cycles. Primary objectives were to assess the effect of docetaxel by comparing EC plus docetaxel versus EC plus TX and to assess the effect of duration by comparing EC plus TX versus EC plus T-X on pathologic complete response (pCR, without invasive/noninvasive breast tumor, regardless of nodal status) at surgery, irrespective of trastuzumab treatment. Results Of 1,509 patients starting EC, 1,421 were randomly assigned to docetaxel (n = 471), TX (n = 471), or T-X (n = 479). At surgery, pCR rates were 22.3%, 19.5%, and 22.3%, respectively; the difference for docetaxel (EC plus docetaxel v EC plus TX) was 2.8% (95% CI, -2.4% to 8.0%; P = .298). The difference for duration was -2.8% (95% CI, -8.0% to 2.4%; P = .298). Breast conservation rates were 70.1%, 68.4%, and 65.3%, respectively (P = .781 for docetaxel; P = .270 for duration). Concomitant but not sequential treatment with docetaxel was associated with more diarrhea; nail changes, and hand-foot-syndrome, but it was associated with less edema. Conclusion Adding capecitabine to or prolonging duration of neoadjuvant EC plus docetaxel does not result in higher efficacy at surgery. J Clin Oncol 28: 2015-2023. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:2015 / 2023
页数:9
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