nab-Paclitaxel plus carboplatin or gemcitabine versus gemcitabine plus carboplatin as first-line treatment of patients with triple-negative metastatic breast cancer: results from the tnAcity trial

被引:92
|
作者
Yardley, D. A. [1 ,2 ]
Coleman, R. [3 ]
Conte, P. [4 ,5 ]
Cortes, J. [6 ,7 ]
Brufsky, A. [8 ]
Shtivelband, M. [9 ]
Young, R. [10 ]
Bengala, C. [11 ]
Ali, H. [12 ]
Eakel, J. [13 ]
Schneeweiss, A. [14 ]
de la Cruz-Merino, L. [15 ]
Wilks, S. [16 ]
O'Shaughnessy, J. [17 ]
Gluck, S. [18 ]
Li, H. [19 ]
Miller, J. [20 ]
Barton, D. [20 ]
Harbeck, N. [21 ]
机构
[1] Sarah Cannon Res Inst, Nashville, TN USA
[2] Tennessee Oncol PLLC, Med Oncol, Nashville, TN USA
[3] Univ Sheffield, Weston Pk Hosp, Dept Oncol & Metab, Sheffield, S Yorkshire, England
[4] Univ Padua, Dept Surg Oncol & Gastroenterol, Padua, Italy
[5] Ist Oncol Veneto, Med Oncol 2, Padua, Italy
[6] Ramon y Cajal Univ Hosp, Med Oncol, Madrid, Spain
[7] Vall dHebron Inst Oncol, Barcelona, Spain
[8] Univ Pittsburgh, Sch Med, Dept Med, Hematol Oncol, Pittsburgh, PA 15213 USA
[9] Ironwood Phys PC, Med Oncol, Chandler, AZ USA
[10] Ctr Canc & Blood Disorders, Med Oncol, Ft Worth, TX USA
[11] Misericordia Gen Hosp, Med Oncol, Grosseto, Italy
[12] Henry Ford Hlth Syst, Med Oncol, Detroit, MI USA
[13] Florida Canc Specialists, Hematol & Oncol, Sarasota, FL USA
[14] Heidelberg Univ Hosp, Gynecol & Med Oncol, Heidelberg, Germany
[15] Hosp Univ Virgen Macarena, Clin Oncol, Seville, Spain
[16] Texas Oncol, Hematol & Med Oncol, San Antonio, TX USA
[17] Texas Oncol, US Oncol, Baylor Sammons Canc Ctr, Hematol,Med Oncol, Dallas, TX USA
[18] Celgene Corp, GMA Early Assets, Summit, NJ USA
[19] Celgene Corp, Dept Biostat, Summit, NJ USA
[20] Celgene Corp, Clin Res & Dev, Hematol Oncol, Summit, NJ USA
[21] Univ Munich, Breast Canc Ctr, Munich, Germany
关键词
chemotherapy; triple-negative breast cancer; nab-paclitaxel; gemcitabine; PHASE-III TRIAL; CHEMOTHERAPY; COMBINATION; BEVACIZUMAB; THERAPY; MODELS;
D O I
10.1093/annonc/mdy201
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Metastatic triple-negative breast cancer (mTNBC) has a poor prognosis and aggressive clinical course. tnAcity evaluated the efficacy and safety of first-line nab-paclitaxel plus carboplatin (nab-P/C), nab-paclitaxel plus gemcitabine (nab-P/G), and gemcitabine plus carboplatin (G/C) in patients with mTNBC. Patients and methods: Patients with pathologically confirmed mTNBC and no prior chemotherapy for metastatic BC received (1 : 1 : 1) nab-P 125 mg/m(2) plus C AUC 2, nab-P 125 mg/m(2) plus G 1000 mg/m(2), or G 1000 mg/m(2) plus C AUC 2, all on days 1, 8 q3w. Phase II primary end point: investigator-assessed progression-free survival (PFS); secondary end points included overall response rate (ORR), overall survival (OS), percentage of patients initiating cycle 6 with doublet therapy, and safety. Results: In total, 191 patients were enrolled (nab-P/C, n = 64; nab-P/G, n = 61; G/C, n = 66). PFS was significantly longer with nab-P/C versus nab-P/G [median, 8.3 versus 5.5 months; hazard ratio (HR), 0.59 [95% CI, 0.38-0.92]; P = 0.02] or G/C (median, 8.3 versus 6.0 months; HR, 0.58 [95% CI, 0.37-0.90]; P = 0.02). OS was numerically longer with nab-P/C versus nab-P/G (median, 16.8 versus 12.1 months; HR, 0.73 [95% CI, 0.47-1.13]; P = 0.16) or G/C (median, 16.8 versus 12.6 months; HR, 0.80 [95% CI, 0.52-1.22]; P = 0.29). ORR was 73%, 39%, and 44%, respectively. In the nab-P/C, nab-P/G, and G/C groups, 64%, 56%, and 50% of patients initiated cycle 6 with a doublet. Grade >= 3 adverse events were mainly hematologic . Conclusions: First-line nab-P/C was active in mTNBC and resulted in a significantly longer PFS and improved risk/benefit profile versus nab-P/G or G/C.
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收藏
页码:1763 / 1770
页数:8
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