...
首页> 外文期刊>Drug Design, Development and Therapy >Brentuximab vedotin for treatment of relapsed or refractory malignant lymphoma: results of a systematic review and meta-analysis of?prospective studies
【24h】

Brentuximab vedotin for treatment of relapsed or refractory malignant lymphoma: results of a systematic review and meta-analysis of?prospective studies

机译:Brentuximab vedotin治疗复发或难治性恶性淋巴瘤的系统评价和前瞻性研究的荟萃分析

获取原文
           

摘要

Background: Recently, brentuximab vedotin has become a promising therapeutic approach for CD30-positive hematological malignancies, but its role in other relapsed or refractory malignant lymphoma needs to be proven. Brentuximab vedotin was demonstrated effective, but no study has summarized the concrete effect of brentuximab vedotin in malignant lymphoma. To truly know the role of brentuximab vedotin, we performed a systematic review of the literature and a meta-analysis of all known prospective trials, to assess the value of brentuximab vedotin for patients with relapsed and refractory malignant lymphoma.Methods and materials: This was a systematic review of publications indexed in the PubMed, Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and ISI Web of Knowledge performed on February?10, 2015. Six studies, including 302 patients were identified. Meta-analyses were carried out to calculate the objective response rate (ORR), complete response rate (CRR), and partial response rate (PRR) of brentuximab vedotin for malignant lymphoma. Results: In patients with malignant lymphoma, ORR was 0.61, CRR was 0.38, and PRR was 0.51. High heterogeneity between studies was observed, and funnel plots were not symmetrical, which means that publication bias existed. Brentuximab vedotin was generally well-tolerated by patients reported in the included studies; adverse effects also occurred, but they were considered manageable.Conclusion: Our analysis revealed a promising benefit of brentuximab vedotin in the treatment of relapsed and refractory malignant lymphoma. Larger sample of randomized controlled clinical trials are needed in the future.
机译:背景:近来,brentuximab vedotin已成为CD30阳性血液学恶性肿瘤的一种有前途的治疗方法,但它在其他复发或难治性恶性淋巴瘤中的作用有待证明。证明了布伦妥昔单抗维多汀有效,但尚无研究总结出布伦妥昔单抗维多汀在恶性淋巴瘤中的具体作用。为了真正了解brentuximab vedotin的作用,我们对文献进行了系统的综述,并对所有已知的前瞻性试验进行了荟萃分析,以评估brentuximab vedotin在复发性和难治性恶性淋巴瘤患者中的价值。对2015年2月10日对PubMed,Embase,Cochrane对照试验中心注册(CENTRAL)和ISI Web of Knowledge编制索引的出版物进行了系统的综述。确定了6项研究,包括302例患者。进行荟萃分析以计算布仑替昔单抗维多汀治疗恶性淋巴瘤的客观缓解率(ORR),完全缓解率(CRR)和部分缓解率(PRR)。结果:恶性淋巴瘤患者的ORR为0.61,CRR为0.38,PRR为0.51。研究之间观察到高度异质性,并且漏斗图不对称,这意味着存在出版偏见。纳入研究报告的患者通常对布伦妥昔单抗vedotin耐受良好;结论:结论:我们的分析显示,brentuximab vedotin在复发性和难治性恶性淋巴瘤的治疗中具有广阔的前景。将来需要更大的随机对照临床试验样本。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号