Weekly paclitaxel with trastuzumab and pertuzumab in patients with HER2-overexpressing metastatic breast cancer: overall survival and updated progression-free survival results from a phase II study

被引:23
作者
Smyth, L. M. [1 ]
Iyengar, N. M. [1 ]
Chen, M. F. [1 ]
Popper, S. M. [1 ]
Patil, S. [2 ]
Wasserheit-Lieblich, C. [3 ]
Argolo, D. F. [4 ]
Singh, J. C. [1 ]
Chandarlapaty, S. [1 ]
Sugarman, S. M. [1 ]
Comen, E. A. [1 ]
Drullinsky, P. R. [1 ]
Traina, T. A. [1 ]
Troso-Sandoval, T. [1 ]
Baselga, J. [1 ]
Norton, L. [1 ]
Hudis, C. A. [1 ]
Dang, C. T. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Breast Serv, Div Solid Tumor Oncol, Dept Med, 300 E 66th St, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY USA
[3] NewYork Presbyterian Lawrence Hosp, New York, NY USA
[4] CLION, Salvador, BA, Brazil
关键词
Breast cancer; Metastatic; HER2; positive; Pertuzumab; Trastuzumab; Paclitaxel; PLUS TRASTUZUMAB; CARDIAC SAFETY; DOCETAXEL; AMPLIFICATION; THERAPY; GROWTH; WOMEN; ERBB2;
D O I
10.1007/s10549-016-3851-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We previously reported progression-free survival (PFS) results on a phase II trial of weekly paclitaxel, trastuzumab, and pertuzumab in patients with human epidermal growth factor receptor 2(HER2)-positive metastatic breast cancer (MBC) treated in the first-and second-line setting. Here, we report results for overall survival (OS) and updated PFS after an additional year of follow-up. Patients with HER2-positive MBC with 0-1 prior treatment were eligible. Treatment consisted of paclitaxel (80 mg/m(2)) weekly, and trastuzumab (loading dose 8 mg/kg -> 6 mg/kg) and pertuzumab (loading dose 840 mg -> 420 mg) every 3 weeks, all given intravenously. Primary endpoint was 6-month PFS. Secondary endpoints included median PFS, 6-month and median OS. Evaluable patients received at least one full dose of treatment. From January 2011 to December 2013, 69 patients were enrolled: 51 (74 %) and 18 (26 %) treated in first-and second-line metastatic settings, respectively. As of July 1, 2015, the median follow-up was 33 months (range 3-49 months; 67 patients were evaluable for efficacy). The median OS was 44 months (95 % CI 37.5-NR) overall and 44 months (95 % CI 38.3-NR) and 37.5 months (95 % CI 30.3-NR) for patients with 0 and 1 prior metastatic treatment, respectively; 6-month OS was 98 % (95 % CI 90-1). The 6-month PFS was 86 % (95 % CI 75-93) overall and 89 % (95 % CI 76-95) and 78 % (95 % CI 51-91) for patients with 0 and 1 prior therapy, respectively; and median PFS was 21.4 months (95 % CI 14.1-NR) overall and 25.7 months (95 % CI 14.1-NR) and 16.9 months (95 % CI 8.5-NR) for patients with 0-1 prior treatment, respectively. Treatment was well tolerated. Updated analysis demonstrates that weekly paclitaxel, when added to trastuzumab and pertuzumab, is associated with a favorable OS and PFS and offers an alternative to docetaxel-based therapy. http://www.ClinicalTrials.gov NCT0127604
引用
收藏
页码:91 / 97
页数:7
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