Docetaxel-cisplatin might be superior to docetaxel-capecitabine in the first-line treatment of metastatic triple-negative breast cancer

被引:75
作者
Fan, Y.
Xu, B. H. [1 ]
Yuan, P.
Ma, F.
Wang, J. Y.
Ding, X. Y.
Zhang, P.
Li, Q.
Cai, R. G.
机构
[1] Chinese Acad Med Sci, Canc Inst & Hosp, Dept Med Oncol, Beijing 100021, Peoples R China
基金
中国国家自然科学基金;
关键词
capecitabine; cisplatin; mBC; triple-negative; PLATINUM-BASED CHEMOTHERAPY; PHASE-II; BRCA1; TRIAL; COMBINATION; EPIRUBICIN; EFFICACY; THERAPY;
D O I
10.1093/annonc/mds603
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Triple-negative breast cancer (TNBC) may be more sensitive to platinum. This study was to compare platinum-based regimen with nonplatinum regimen in the first-line treatment of advanced TNBC. Patients and methods: Eligible metastatic TNBC (mTNBC) women without prior treatment for advanced disease were randomized (1 : 1) to receive either docetaxel-cisplatin (TP) or docetaxel -capecitabine (TX) q3w for up to 6 cycles, until disease progression or unacceptable toxicity. The primary end point was objective response rate (ORR) and the secondary end points included progression-free survival (PFS) and overall survival (OS). In total 53 patients were enrolled. Results: The median follow-up was 24 months. ORR was higher in the TP group than in the TX group (63.0% versus 15.4%, P = 0.001). PFS was more than doubled (10.9 months versus 4.8 months, P < 0.001) and median OS was also greatly improved (32.8 months versus 21.5 months, P = 0.027). Toxic effects were not different except G3/4 vomiting and G2/3 hand-foot syndrome. Conclusions: This study suggested that cisplatin-based chemotherapy was superior to capecitabine-based regimen in the first-line treatment of mTNBC, as measured by ORR, PFS and OS. Further large-scale study should be warranted. These results are not sufficient to change clinical practice.
引用
收藏
页码:1219 / 1225
页数:8
相关论文
共 31 条
[1]   Docetaxel and cisplatin combination chemotherapy in metastatic breast cancer patients with previous exposure to anthracyclines [J].
Ahn, JH ;
Kim, SB ;
Sohn, HJ ;
Lee, JS ;
Kang, YK ;
Kim, WK .
BREAST, 2005, 14 (04) :304-309
[2]  
[Anonymous], 2003, COMM TERM CRIT ADV E
[3]   Descriptive analysis of estrogen receptor (ER)negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype - A population-based study from the California Cancer Registry [J].
Bauer, Katrina R. ;
Brown, Monica ;
Cress, Rosemary D. ;
Parise, Carol A. ;
Caggiano, Vincent .
CANCER, 2007, 109 (09) :1721-1728
[4]   The breast cancer susceptibility gene BRCA1 is required for subnuclear assembly of Rad51 and survival following treatment with the DNA cross-linking agent cisplatin [J].
Bhattacharyya, A ;
Ear, US ;
Koller, BH ;
Weichselbaum, RR ;
Bishop, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23899-23903
[5]   Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients [J].
Byrski, T. ;
Huzarski, T. ;
Dent, R. ;
Gronwald, J. ;
Zuziak, D. ;
Cybulski, C. ;
Kladny, J. ;
Gorski, B. ;
Lubinski, J. ;
Narod, S. A. .
BREAST CANCER RESEARCH AND TREATMENT, 2009, 115 (02) :359-363
[6]   Pattern of metastatic spread in triple-negative breast cancer [J].
Dent, Rebecca ;
Hanna, Wedad M. ;
Trudeau, Maureen ;
Rawlinson, Ellen ;
Sun, Ping ;
Narod, Steven A. .
BREAST CANCER RESEARCH AND TREATMENT, 2009, 115 (02) :423-428
[7]   CISPLATIN IN THE TREATMENT OF METASTATIC BREAST-CARCINOMA - A PROSPECTIVE RANDOMIZED TRIAL OF 2 DOSAGE SCHEDULES [J].
FORASTIERE, AA ;
HAKES, TB ;
WITTES, JT ;
WITTES, RE .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1982, 5 (03) :243-247
[8]   Preoperative weekly cisplatin-epirubicin-paclitaxel with G-CSF support in triple-negative large operable breast cancer [J].
Frasci, G. ;
Comella, P. ;
Rinaldo, M. ;
Iodice, G. ;
Di Bonito, M. ;
D'Aiuto, M. ;
Petrillo, A. ;
Lastoria, S. ;
Siani, C. ;
Comella, G. ;
D'Aiuto, G. .
ANNALS OF ONCOLOGY, 2009, 20 (07) :1185-1192
[9]   Adjuvant Capecitabine, Docetaxel, Cyclophosphamide, and Epirubicin for Early Breast Cancer: Final Analysis of the Randomized FinXX Trial [J].
Joensuu, Heikki ;
Kellokumpu-Lehtinen, Pirkko-Liisa ;
Huovinen, Riikka ;
Jukkola-Vuorinen, Arja ;
Tanner, Minna ;
Kokko, Riitta ;
Ahlgren, Johan ;
Auvinen, Paivi ;
Paija, Outi ;
Helle, Leena ;
Villman, Kenneth ;
Nyandoto, Paul ;
Nilsson, Greger ;
Pajunen, Marjo ;
Asola, Raija ;
Poikonen, Paula ;
Leinonen, Mika ;
Kataja, Vesa ;
Bono, Petri ;
Lindman, Henrik .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (01) :11-18
[10]   The role of BRCA1 in the cellular response to chemotherapy [J].
Kennedy, RD ;
Quinn, JE ;
Mullan, PB ;
Johnston, PG ;
Harkin, DP .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (22) :1659-1668