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长春瑞滨用于恶性胸膜间皮瘤患者的II期研究。

Phase II study of vinorelbine in patients with malignant pleural mesothelioma.

作者信息

Steele J P, Shamash J, Evans M T, Gower N H, Tischkowitz M D, Rudd R M

机构信息

Department of Medical Oncology, St Bartholomew's Hospital, and the London Lung Cancer Group, London, United Kingdom.

出版信息

J Clin Oncol. 2000 Dec 1;18(23):3912-7. doi: 10.1200/JCO.2000.18.23.3912.

DOI:10.1200/JCO.2000.18.23.3912
PMID:11099320
Abstract

PURPOSE

To evaluate the response rate and impact on quality of life of vinorelbine given as cycles of 30 mg/m(2) weekly for 6 weeks to patients with malignant pleural mesothelioma.

PATIENTS AND METHODS

Twenty-nine patients with histologically proven malignant pleural mesothelioma were enrolled (26 male patients and three female patients; median age, 58 years [range, 29 to 77 years]). Seventeen patients had epithelioid tumors, two had sarcomatoid tumors, and 10 had biphasic tumors. The International Mesothelioma Interest Group staging system was used: one patient had stage Ib disease, 10 had stage II disease, eight had stage III disease, and 10 had stage IV disease. Patients were treated with weekly injections of vinorelbine 30 mg/m(2). A cycle consisted of six weekly injections. The new guidelines to evaluate the response to treatment in solid tumors were used. Responses were measured by spiral computed tomography scan.

RESULTS

All twenty-nine patients had measurable disease and were assessed for response. There were seven partial responses (24% [95% confidence interval, 10% to 44%]), 16 patients had stable disease (55%), and six patients had disease progression on therapy (21%). The median number of vinorelbine injections was 12 (range, 2 to 30). Quality-of-life analyses showed a benefit for vinorelbine therapy.

CONCLUSION

Vinorelbine shows promise in the palliation of patients with malignant pleural mesothelioma. The relatively low toxicity of the drug suggests that trials of vinorelbine in combination with other agents should be feasible.

摘要

目的

评估长春瑞滨以30mg/m²的剂量每周给药一次,共6周,对恶性胸膜间皮瘤患者的缓解率及对生活质量的影响。

患者与方法

纳入29例经组织学证实的恶性胸膜间皮瘤患者(26例男性患者和3例女性患者;中位年龄58岁[范围29至77岁])。17例患者为上皮样肿瘤,2例为肉瘤样肿瘤,10例为双向肿瘤。采用国际间皮瘤兴趣小组分期系统:1例患者为Ib期疾病,10例为II期疾病,8例为III期疾病,10例为IV期疾病。患者接受每周一次30mg/m²长春瑞滨的注射治疗。一个疗程包括6次每周注射。采用实体瘤治疗反应评估新指南。通过螺旋计算机断层扫描测量反应。

结果

所有29例患者均有可测量的疾病并接受反应评估。有7例部分缓解(24%[95%置信区间,10%至44%]),16例患者疾病稳定(55%),6例患者在治疗中疾病进展(21%)。长春瑞滨注射的中位次数为12次(范围2至30次)。生活质量分析显示长春瑞滨治疗有益。

结论

长春瑞滨在恶性胸膜间皮瘤患者的姑息治疗中显示出前景。该药物相对较低的毒性表明长春瑞滨与其他药物联合试验应是可行的。

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