Randomized phase III trial of pegylated liposomal doxorubicin versus vinorelbine or mitomycin C plus vinblastine in women with taxane-refractory advanced breast cancer

被引:167
作者
Keller, AM
Mennel, R
Georgoulias, VA
Nabholtz, JM
Erazo, A
Lluch, A
Vogel, CL
Kaufmann, M
von Minckwitz, G
Henderson, IC
Mellars, L
Alland, L
Tendler, C
机构
[1] US Oncol Inc, Canc Care Associates, Tulsa, OK 74136 USA
[2] US Oncol, Dallas, TX USA
[3] Univ Hosp Herakl, Iraklion, Crete, Greece
[4] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[5] Ctr Med Nacl, ISSSTE, Mexico City, DF, Mexico
[6] Univ Valencia, Hosp Clin, Valencia, Spain
[7] Aventura Concorde Ctr 2, Aventura, FL USA
[8] Univ Frankfurt, Dept Gynecol & Obstet, D-6000 Frankfurt, Germany
[9] Univ Calif San Francisco, San Francisco, CA 94143 USA
[10] Schering Plough Res Inst, Kenilworth, NJ USA
关键词
D O I
10.1200/JCO.2004.08.157
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To compare the efficacy of pegylated liposomal doxorubicin (PLD) with that of a common salvage regimen (comparator) in patients with taxane-refractory advanced breast cancer. Patients and Methods Following failure of a first- or second-line taxane-containing regimen for metastatic disease, 301 women were randomly assigned to receive PLD (50 mg/m(2) every 28 days); or comparator-vinorelbine (30 mg/m(2) weekly) or mitomycin C (10 mg/m(2) day 1 and every 28 days) plus vinblastine (5 mg/m(2) day 1, day 14, day 28, and day 42) every 6 to 8 weeks. Patients were stratified before random assignment based on number of previous chemotherapy regimens for metastatic disease and presence of bone metastases only. Results Progression-free survival (PFS) and overall survival (OS) were similar for PLD and comparator (PFS: hazard ratio [HR], 1.26; 95% Cl, 0.98 to 1.62; P = .11; median, 2.9 months [PLD] and 2.5 months [comparator]; OS: HR, 1.05; 95% Cl, 0.82 to 1.33; P = .71; median, 11.0 months [PLD] and 9.0 months [comparator]). In anthracycline-naive patients, PFS was somewhat longer with PLD, relative to the comparator (n = 44; median PFS, 5.8 v 2.1 months; HR, 2.40; 95% Cl, 1.16 to 4.95; P = .01). Most frequently reported adverse events were nausea (23% to 31%), vomiting (17% to 20%), and fatigue (9% to 20%) and were similar among treatment groups. PLD-treated patients experienced more palmar-plantar erythrodysesthesia (37%; 18% grade 3, 1 patient grade 4) and stomatitis (22%; 5% grades 3/4). Neuropathy (11%), constipation (16%), and neutropenia (14%) were more common with vinorelbine. Alopecia was low in both the PLD and vinorelbine groups (3% and 5%). Conclusion PLD has efficacy comparable to that of common salvage regimens in patients with taxane-refractory metastatic breast cancer, thereby representing a useful therapeutic option. (C) 2004 by American Society of Clinical Oncology.
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页码:3893 / 3901
页数:9
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