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利妥昔单抗在类固醇难治性慢性移植物抗宿主病中的疗效:一项系统评价和荟萃分析。

Efficacy of rituximab in the setting of steroid-refractory chronic graft-versus-host disease: a systematic review and meta-analysis.

作者信息

Kharfan-Dabaja Mohamed A, Mhaskar Asmita R, Djulbegovic Benjamin, Cutler Corey, Mohty Mohamad, Kumar Ambuj

机构信息

Department of Blood and Marrow Transplantation, Moffitt Cancer Center, Tampa, Florida, USA.

出版信息

Biol Blood Marrow Transplant. 2009 Sep;15(9):1005-13. doi: 10.1016/j.bbmt.2009.04.003. Epub 2009 Jun 10.

Abstract

Increased insight into the role of B lymphocytes in the pathophysiology of graft-versus-host disease has led to a number of studies assessing the efficacy of the anti-CD20 monoclonal antibody (mAb) rituximab in treating steroid-refractory chronic graft-versus-host disease (cGVHD). Findings vary greatly among these studies, however. We conducted a systematic review to summarize the totality of evidence on the efficacy of rituximab in steroid-refractory cGVHD. We performed a PubMed search and contacted experts in the field to identify relevant studies. Endpoints included overall response rate (including organ-specific) and ability of rituximab to allow dosage reduction of immunosuppressive therapies. Data were pooled under a random-effects model. Seven studies (3 prospective and 4 retrospective, with a total of 111 patients) met the inclusion criteria. The pooled proportion of overall response was 0.66 (95% confidence interval=0.57 to 0.74). There was no heterogeneity among the pooled studies. Response rates were 13% to 100% for cGVHD of the skin, 0 to 83% for cGVHD of the oral mucosa, 0 to 66% for cGVHD of the liver, and 0 to 38% for cGVHD of the lung. Common adverse events were related to infusion reactions or infectious complications. The relatively small number of patients and the varying criteria for reporting organ response and dosage reduction of steroids, among other limitations, hinders our ability to reach definitive conclusions on the overall efficacy of rituximab for cGVHD involving other organs.

摘要

对B淋巴细胞在移植物抗宿主病病理生理学中作用的深入了解,促使了多项研究评估抗CD20单克隆抗体(mAb)利妥昔单抗治疗类固醇难治性慢性移植物抗宿主病(cGVHD)的疗效。然而,这些研究的结果差异很大。我们进行了一项系统综述,以总结利妥昔单抗治疗类固醇难治性cGVHD疗效的全部证据。我们在PubMed上进行了检索,并联系了该领域的专家以确定相关研究。终点指标包括总缓解率(包括器官特异性缓解率)以及利妥昔单抗使免疫抑制治疗剂量减少的能力。数据采用随机效应模型进行汇总。七项研究(3项前瞻性研究和4项回顾性研究,共111例患者)符合纳入标准。汇总后的总缓解比例为0.66(95%置信区间=0.57至0.74)。汇总研究之间不存在异质性。皮肤cGVHD的缓解率为13%至100%,口腔黏膜cGVHD的缓解率为0至83%,肝脏cGVHD的缓解率为0至66%,肺部cGVHD的缓解率为0至38%。常见的不良事件与输液反应或感染并发症有关。除其他局限性外,患者数量相对较少以及报告器官反应和类固醇剂量减少的标准各不相同,这妨碍了我们就利妥昔单抗对涉及其他器官的cGVHD的总体疗效得出明确结论。

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