The efficacy and safety of weekly vinorelbine in relapsed malignant pleural mesothelioma

被引:118
|
作者
Stebbing, Justin [1 ]
Powles, Thomas [1 ]
McPherson, Kirsty [1 ]
Shamash, Jonathan [1 ]
Wells, Paula [2 ]
Sheaff, Michael T. [3 ]
Slater, Sarah [1 ]
Rudd, Robin M. [1 ]
Fennell, Dean [1 ]
Steele, Jeremy P. C. [1 ]
机构
[1] St Bartholomews Hosp, Dept Med Oncol, London EC1A 7BE, England
[2] St Bartholomews Hosp, Dept Radiotherapy, London EC1A 7BE, England
[3] Royal London Hosp, Dept Pathol, Inst Cell & Mol Sci, London E1 1BB, England
关键词
Mesothelioma; Relapsed; Vinorelbine; Second-line; NATIONAL-CANCER-INSTITUTE; RANDOMIZED PHASE-III; LUNG-CANCER; PERITONEAL MESOTHELIOMA; 2ND-LINE CHEMOTHERAPY; CISPLATIN; COMBINATION; THERAPY; GEMCITABINE; OXALIPLATIN;
D O I
10.1016/j.lungcan.2008.04.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant pleural mesothelioma (MPM) is a rapidly progressive invariably lethal tumor. Treatment options remain limited and the outcome in relapsed disease is poor warranting new therapeutic options. Following our previous experience in the first-line setting, we conducted a phase 2 open-label non-comparative study to assess the safety and efficacy of weekly vinorelbine chemotherapy, each cycle consisting of 30 mg/m(2) for 6 weeks, in patients with previous exposure to chemotherapy. In 63 individuals with relapsed MPM who had not received previous vinorelbine, we observed an objective response rate of 16% and an overall survival of 9.6 months (95% confidence interval 7.3-11.8 months). The main grade III/IV toxicity observed was neutropenia and toxicity was similar to weekly vinorelbine when used in the first-line setting. Weekly vinorelbine appeared to have a reasonable response rate with an acceptable toxicity profile in the second-line treatment of MPM. Its use should be prospectively evaluated in a randomised trial in the first or second-line therapy of MPM. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:94 / 97
页数:4
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