A Phase II Trial of Nab-Paclitaxel (ABI-007) and Carboplatin in Patients With Unresectable Stage IV Melanoma A North Central Cancer Treatment Group Study, N057E

被引:78
|
作者
Kottschade, Lisa A. [1 ]
Suman, Vera J. [1 ]
Amatruda, Thomas, III [2 ]
McWilliams, Robert R. [1 ]
Mattar, Bassam I. [3 ]
Nikcevich, Daniel A. [4 ]
Behrens, Robert [5 ]
Fitch, Tom R. [6 ]
Jaslowski, Anthony J. [7 ]
Markovic, Svetomir N. [1 ]
机构
[1] Mayo Clin, Rochester, MN 55905 USA
[2] Metro Minnesota Community Clin Oncol Program, St Louis Pk, MN USA
[3] Wichita Community Clin Oncol, Wichita, KS USA
[4] Duluth CCOP, Duluth, MN USA
[5] Iowa Oncol Res Assoc CCOP, Des Moines, IA USA
[6] Mayo Clin, Scottsdale, AZ USA
[7] St Vincent Reg Canc Ctr CCOP, Green Bay, WI USA
关键词
metastatic melanoma; nab-paclitaxel; carboplatin; chemotherapy; stage IV; unresectable; ALBUMIN-BOUND PACLITAXEL; METASTATIC MELANOMA; MALIGNANT-MELANOMA; 2ND-LINE THERAPY; DACARBAZINE; COMBINATION; CISPLATIN; BEVACIZUMAB; TAMOXIFEN; REGIMEN;
D O I
10.1002/cncr.25659
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: There is increasing evidence that paclitaxel and carboplatin are clinically active in the treatment of metastatic melanoma (MM). ABI-007 is an albumin-bound formulation of paclitaxel that has demonstrated single-agent activity against metastatic melanoma. METHODS: A parallel phase II trial was conducted in patients with unresectable stage IV melanoma who were either chemotherapy naive (CN) or previously treated (PT). The treatment regimen consisted of ABI-007 (100 mg/m(2)) and carboplatin area under the curve (AUC2) administered on days 1, 8, and 15 every 28 days. The primary aim of this study was objective response rate (RECIST). RESULTS: Seventy-six patients (41 CN and 35 PT) were enrolled between November 2006 and July 2007. Three patients withdrew consent prior to starting treatment. The median number of treatment cycles was 4. There were 10 (25.6%) responses (1 complete response [CR] and 9 partial responses [PRs]) in the CN cohort (90% CI, 16.7%-42.3%) and 3 (8.8%) responses (3 PRs) in the PT cohort (90% CI, 2.5%-21.3%). Median progression-free survival was 4.5 months in the CN cohort and 4.1 months in the PT cohort. Median overall survival (OS) was 11.1 months in the CN group and 10.9 months in the PT group. Severe toxicities in both groups (Common Terminology Criteria for Adverse Effects v.3.0 >= grade 3) included neutropenia, thrombocytopenia, neurosensory problems, fatigue, nausea, and vomiting. CONCLUSIONS: The weekly combination of ABI-007 and carboplatin appears to be moderately well tolerated, with promising clinical activity as therapy in patients who are chemotherapy naive and with modest antitumor activity in those previously treated. Cancer 2011;117:1704-10. (C) 2010 American Cancer Society.
引用
收藏
页码:1704 / 1710
页数:7
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