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利妥昔单抗在急性淋巴细胞白血病治疗中的应用。

Rituximab in the management of acute lymphoblastic leukemia.

机构信息

a Department Hematology-Oncology , Azienda Ospedaliera Pugliese-Ciaccio , Catanzaro , Italy.

出版信息

Expert Opin Biol Ther. 2018 Feb;18(2):221-226. doi: 10.1080/14712598.2018.1425389. Epub 2018 Jan 17.

Abstract

The anti-CD20 chimeric monoclonal antibody rituximab has revolutionized the treatment of B-cell malignancies, significantly improving patient clinical outcome. Recently, some single-group studies have suggested that adding rituximab to chemotherapy can improve the outcome of CD20-positive B-cell acute lymphoblastic leukemia (ALL) patients. Areas covered: An overview of the current insights of rituximab in adult ALL patients is presented here. In particular, we focused on results of multicenter randomized phase III trial (GRAALL-2005 - Group for Research on Adult Acute Lymphoblastic Leukemia) that evaluated the benefit of associating rituximab to chemotherapy in Ph-negative, B-lineage ALL expressing the CD20 antigen. Expert opinion: Data from clinical trials confirm that rituximab enhances the efficacy of chemotherapy without additive toxicity in ALL. However, results of GRAAL 2005 study represent only a modest incremental improvement in the treatment of ALL. Other promising compounds as single agent or in combination with chemotherapy are currently in different stages of clinical development. The GRAALL 2005 study sets the stage for other prospective studies which will further elucidate the role of monoclonal antibodies in the management of ALL.

摘要

抗 CD20 嵌合单克隆抗体利妥昔单抗彻底改变了 B 细胞恶性肿瘤的治疗方法,显著改善了患者的临床预后。最近,一些单组研究表明,在化疗中加入利妥昔单抗可以改善 CD20 阳性 B 细胞急性淋巴细胞白血病(ALL)患者的预后。

涵盖领域

本文介绍了利妥昔单抗在成人 ALL 患者中的最新研究进展。特别关注了多中心随机 III 期试验(GRAALL-2005 - 成人急性淋巴细胞白血病研究组)的结果,该试验评估了在 Ph 阴性、表达 CD20 抗原的 B 细胞 ALL 中联合使用利妥昔单抗与化疗的益处。

专家意见

临床试验数据证实,利妥昔单抗在不增加化疗毒性的情况下增强了 ALL 的疗效。然而,GRAAL 2005 研究的结果仅代表 ALL 治疗的适度增量改善。其他有前途的化合物作为单一药物或与化疗联合使用,目前处于不同的临床开发阶段。GRAALL 2005 研究为其他前瞻性研究奠定了基础,这些研究将进一步阐明单克隆抗体在 ALL 治疗中的作用。

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