Phase I/II study of ixabepilone plus capecitabine in anthracycline-pretreated/resistant and taxane-resistant metastatic breast cancer

被引:49
作者
Bunnell, Craig [1 ]
Vahdat, Linda [2 ]
Schwartzberg, Lee [3 ]
Gralow, Julie [4 ]
Klimovsky, Judith [5 ]
Poulart, Valerie [6 ]
Peck, Ronald [6 ]
Thomas, Eva [7 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Weill Cornell Breast Ctr, New York, NY USA
[3] W Canc Clin, Memphis, TN USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[5] Merck & Co Inc, Somerset, NJ USA
[6] Bristol Myers Squibb Co, Res & Dev, Oakland, CA USA
[7] Kaiser Permanente, Oakland, CA USA
关键词
epothilones; maximum tolerated dose; microtubule inhibitors;
D O I
10.3816/CBC.2008.n.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this study was to determine the safety, maximum tolerated dose (MTD), recommended phase II dose, and efficacy of the epothilone B analogue ixabepilone plus capecitabine in anthracycline-pretreated/resistant and taxane-resistant metastatic breast cancer (MBC). Patients and Methods: A total of 106 patients were enrolled. The study consisted of a dose-escalation phase (phase I) and a tumor response rate evaluation phase (phase II). Seventy-four patients were treated in phase I with schedule A (ixabepilone 40 mg/m(2) intravenously on day 1 plus capecitabine 1650-2000 mg/m(2) on days 1-14 of a 21-day cycle) or schedule B (ixabepilone 8-10 mg/m(2) on days 1-3 plus capecitabine 1650 mg/m(2) on days 1-14 of a 21-day cycle). Results: No dose-limiting toxicities (DLTs) were observed in the 8/1650 mg/m(2) and 10/1650 mg/m(2) cohorts; 1 of 30 patients in the 40/1650 mg/m(2) cohort and 2 of 30 patients in the 40/2000 mg/m(2) cohort had a DLT consisting of grade 3 plantar-palmar erythrodysesthesia (PPE). The 40/2000 mg/m(2) dose was defined as the MTD for schedule A, and a total of 62 patients were treated for the phase II portion of the trial, which examined tumor response. The objective response rate was 30%, median time-to-response was 6 weeks, median duration of response was 6.9 months, and median progression-free survival was 3.8 months. Grade 3/4 treatment-related events in phase II included fatigue (34%), PPE (34%), myalgia (23%), nausea (16%), peripheral neuropathy (19%), and diarrhea/vomiting (10%). Grades 3/4 neutropenia (69%) and leukopenia (55%) were managed primarily by dose reduction/treatment interruption. Conclusion: Ixabepilone plus capecitabine demonstrated clinical activity and an acceptable safety profile in patients with anthracycline-pretreated/resistant and taxane-resistant MBC. Ixabepilone was recently approved in the United States for the treatment of resistant/refractory locally advanced or MBC.
引用
收藏
页码:234 / 241
页数:8
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