Ixabepilone, Mitoxantrone, and Prednisone for Metastatic Castration-Resistant Prostate Cancer After Docetaxel-Based Therapy A Phase 2 Study of the Department of Defense Prostate Cancer Clinical Trials Consortium

被引:9
作者
Harzstark, Andrea L. [1 ]
Rosenberg, Jonathan E. [2 ]
Weinberg, Vivian K.
Sharib, Jeremy
Ryan, Charles J.
Smith, David C. [3 ]
Pagliaro, Lance C. [4 ]
Beer, Tomasz M. [5 ]
Liu, Glenn [6 ]
Small, Eric J.
机构
[1] Univ Calif San Francisco, Dept Med, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Univ Michigan, Ann Arbor, MI 48109 USA
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[5] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97201 USA
[6] Univ Wisconsin, Carbone Canc Ctr, Madison, WI USA
关键词
prostate cancer; chemotherapy; metastatic; mitoxantrone; ixabepilone; docetaxel; EPOTHILONE-B ANALOG; ADVANCED BREAST-CANCER; WORKING GROUP; BMS-247550; RECOMMENDATIONS; ANTHRACYCLINE; CHEMOTHERAPY; ANTIGEN; TAXANE;
D O I
10.1002/cncr.25810
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Mitoxantrone plus prednisone and ixabepilone each have modest activity as monotherapy for second-line chemotherapy in patients with docetaxel-refractory castration-resistant prostate cancer. Clinical noncross-resistance was previously observed. Phase 1 testing determined the maximum tolerated dose and dose-limiting toxicities with the combination regimen; a phase 2 study was conducted to evaluate the activity of the combination. METHODS: Patients with metastatic progressive castration-resistant prostate cancer during or after 3 or more cycles of taxane-based chemotherapy enrolled in a phase 2 multicenter study of ixabepilone 35 mg/m(2) and mitoxantrone 12 mg/m(2) administered on Day 1 every 21 days with pegfilgrastim support, along with prednisone 5 mg twice daily. Patients were evaluated for disease response and toxicity. RESULTS: Results are reported for the 56 evaluable patients. Twenty-five (45%; 95% confidence interval [CI], 31%-59%) experienced confirmed >= 50% prostate-specific antigen (PSA) declines, 33 (59%; 95% CI, 45%-72%) experienced confirmed >= 30% PSA declines, and 8 of 36 patients (22%; 95% CI, 10%-39%) with measurable disease experienced objective responses. Median time to PSA or objective progression was 4.4 months (95% CI, 3.5-5.6), and median progression-free survival was also 4.4 months (95% CI, 3.0-6.0). Median overall survival was 12.5 months (95% CI, 10.2-15.9). Thirty-two percent of patients experienced grade 3 of 4 neutropenia, and 11% experienced grade 3 or higher neutropenic infections, including 1 treatment-related death. Grade 2 and 3 neuropathy occurred in 11% and 12.5% of patients, respectively. CONCLUSIONS: These results suggest that the combination of ixabepilone and mitoxantrone is both feasible and active in castration-resistant prostate cancer and requires dosing with pegfilgrastim. Cancer 2011; 117: 2419-25. (C) 2010 American Cancer Society.
引用
收藏
页码:2419 / 2425
页数:7
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