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首页> 外文期刊>The Lancet >Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial.
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Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial.

机译:在有或没有化疗的情况下对症状性活动进行控制以治疗恶性胸膜间皮瘤(MS01):一项多中心随机试验。

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BACKGROUND: Malignant pleural mesothelioma is almost always fatal, and few treatment options are available. Although active symptom control (ASC) has been recommended for the management of this disease, no consensus exists for the role of chemotherapy. We investigated whether the addition of chemotherapy to ASC improved survival and quality of life. METHODS: 409 patients with malignant pleural mesothelioma, from 76 centres in the UK and two in Australia, were randomly assigned to ASC alone (treatment could include steroids, analgesic drugs, bronchodilators, palliative radiotherapy [n=136]); to ASC plus MVP (four cycles of mitomycin 6 mg/m2, vinblastine 6 mg/m2, and cisplatin 50 mg/m2 every 3 weeks [n=137]); or to ASC plus vinorelbine (one injection of vinorelbine 30 mg/m2 every week for 12 weeks [n=136]). Randomisation was done by minimisation, with stratification for WHO performance status, histology, and centre. Follow-up was every 3 weeks to 21 weeks after randomisation, and every 8 weeks thereafter. Because of slow accrual, the two chemotherapy groups were combined and compared with ASC alone for the primary outcome of overall survival. Analysis was by intention to treat. This study is registered, number ISRCTN54469112. FINDINGS: At the time of analysis, 393 (96%) patients had died (ASC 132 [97%], ASC plus MVP 132 [96%], ASC plus vinorelbine 129 [95%]). Compared with ASC alone, we noted a small, non-significant survival benefit for ASC plus chemotherapy (hazard ratio [HR] 0.89 [95% CI 0.72-1.10]; p=0.29). Median survival was 7.6 months in the ASC alone group and 8.5 months in the ASC plus chemotherapy group. Exploratory analyses suggested a survival advantage for ASC plus vinorelbine compared with ASC alone (HR 0.80 [0.63-1.02]; p=0.08), with a median survival of 9.5 months. There was no evidence of a survival benefit with ASC plus MVP (HR 0.99 [0.78-1.27]; p=0.95). We observed no between-group differences in four predefined quality-of-life subscales (physical functioning, pain, dyspnoea, and global health status) at any of the assessments in the first 6 months. INTERPRETATION: The addition of chemotherapy to ASC offers no significant benefits in terms of overall survival or quality of life. However, exploratory analyses suggested that vinorelbine merits further investigation.
机译:背景:恶性胸膜间皮瘤几乎总是致命的,很少有治疗选择。尽管已建议采用主动症状控制(ASC)来治疗该疾病,但对于化疗的作用尚无共识。我们调查了在ASC中添加化疗是否可以改善生存率和生活质量。方法:将来自英国76个中心和澳大利亚两个中心的409例恶性胸膜间皮瘤患者随机分配至ASC(治疗可包括类固醇,镇痛药,支气管扩张药,姑息性放疗[n = 136]); ASC加MVP(每3周进行四个周期的丝裂霉素6 mg / m2,长春碱6 mg / m2和顺铂50 mg / m2 [n = 137]);或ASC加长春瑞滨(长春瑞滨30毫克/平方米每星期注射一次,持续12周[n = 136])。通过最小化进行随机分组,并根据WHO的表现状态,组织学和中心进行分层。随机分组后每3周至21周进行一次随访,此后每8周进行一次随访。由于进展缓慢,因此将两个化疗组合并,并与单独的ASC进行比较,以求出总体生存率的主要结果。分析是按意向进行的。该研究已注册,编号ISRCTN54469112。结果:在分析时,有393名(96%)患者死亡(ASC 132 [97%],ASC加MVP 132 [96%],ASC加长春瑞滨129 [95%])。与单独的ASC相比,我们注意到ASC加化学疗法的生存获益很小,并不显着(危险比[HR] 0.89 [95%CI 0.72-1.10]; p = 0.29)。单纯ASC组中位生存期为7.6个月,ASC加化疗组中位生存期为8.5个月。探索性分析表明,与单独使用ASC相比,ASC加长春瑞滨具有生存优势(HR 0.80 [0.63-1.02]; p = 0.08),中位生存期为9.5个月。没有证据显示ASC加MVP有生存益处(HR 0.99 [0.78-1.27]; p = 0.95)。我们在头6个月的任何评估中都没有观察到四个预定义的生活质量分量表(身体功能,疼痛,呼吸困难和整体健康状况)的组间差异。解释:在ASC中增加化疗对总体生存或生活质量没有明显的益处。然而,探索性分析表明长春瑞滨值得进一步研究。

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