Suppr超能文献

含利妥昔单抗的缓解诱导疗法显著改善了初治成熟B细胞淋巴瘤的治疗效果。

Remission induction therapy containing rituximab markedly improved the outcome of untreated mature B cell lymphoma.

作者信息

Nagai Hirokazu, Yano Takahiro, Watanabe Tomoyuki, Uike Naokuni, Okamura Seiichi, Hanada Shuichi, Kawano Fumio, Sunami Kazutaka, Inoue Nobumasa, Sawamura Morio, Nishiura Tetsuo, Hotta Tomomitsu, Horibe Keizo

机构信息

Clinical Research Centre, National Hospital Organization Nagoya Medical Centre, Nagoya, Japan.

出版信息

Br J Haematol. 2008 Dec;143(5):672-80. doi: 10.1111/j.1365-2141.2008.07390.x. Epub 2008 Oct 20.

Abstract

Many controlled clinical trials have proven that rituximab improves the clinical outcome of patients with mature B cell lymphoma. This study was conducted to assess the contribution of rituximab in the actual clinical practice. Patients with newly diagnosed mature B cell lymphoma treated at 20 National Hospital Organization hospitals from January 2000 to December 2004 were consecutively registered. Rituximab was approved in September 2002 for indolent B cell lymphoma and in September 2003 for aggressive B cell lymphoma in Japan. The patients were divided into two groups depending on whether they received induction therapy containing rituximab. The endpoint was to evaluate the rituximab benefit based on 2-year progression-free survival (PFS) and 2-year overall survival (OS). A total 1126 patients received chemotherapies. Of these, 762 were diagnosed as diffuse large B cell lymphoma (DLBCL) and 215 as follicular lymphoma (FL). PFS and OS were markedly improved in the rituximab group compared with the non-rituximab group in patients with DLBCL (both P < 0.001) and in patients with FL (P < 0.001 and P = 0.003 respectively). Rituximab, when used for remission induction therapy, significantly improved the clinical outcome of the mature B cell lymphoma patient in actual clinical practice.

摘要

许多对照临床试验已证明利妥昔单抗可改善成熟B细胞淋巴瘤患者的临床结局。本研究旨在评估利妥昔单抗在实际临床实践中的作用。对2000年1月至2004年12月期间在20家国立医院机构接受治疗的新诊断成熟B细胞淋巴瘤患者进行连续登记。在日本,利妥昔单抗于2002年9月被批准用于惰性B细胞淋巴瘤,2003年9月被批准用于侵袭性B细胞淋巴瘤。根据患者是否接受含利妥昔单抗的诱导治疗将其分为两组。终点是基于2年无进展生存期(PFS)和2年总生存期(OS)评估利妥昔单抗的益处。共有1126例患者接受了化疗。其中,762例被诊断为弥漫性大B细胞淋巴瘤(DLBCL),215例为滤泡性淋巴瘤(FL)。在DLBCL患者(均P<0.001)和FL患者中(分别为P<0.001和P = 0.003),利妥昔单抗组的PFS和OS与非利妥昔单抗组相比均有显著改善。在实际临床实践中,利妥昔单抗用于缓解诱导治疗时,可显著改善成熟B细胞淋巴瘤患者的临床结局。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验