Suppr超能文献

新型药物对T细胞淋巴瘤患者异基因造血细胞移植的影响

Impact of Novel Agents on Allogeneic Hematopoietic Cell Transplantation in Patients with T-Cell Lymphomas.

作者信息

Inoue Yoshitaka, Yasunaga Jun-Ichirou

机构信息

Blood and Marrow Transplant Program, Division of Hematology and Oncology, Penn State Cancer Institute, Hershey, PA 17033, USA.

Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.

出版信息

Cells. 2025 Aug 23;14(17):1306. doi: 10.3390/cells14171306.

Abstract

T-cell lymphomas (TCLs) are generally associated with a poorer prognosis compared to B-cell lymphomas, and allogeneic hematopoietic cell transplantation (allo-HCT) is often considered for eligible patients. One of the primary reasons for the inferior outcomes in TCLs has been the lack of effective novel agents for many years, resulting in a continued reliance on traditional cytotoxic chemotherapy regimens. However, over the past decade, several novel agents with promising efficacy against TCLs have been developed. Notably, many of these agents not only exert direct anti-tumor effects but also modulate host immune function, raising clinical questions regarding the optimal integration of these agents with allo-HCT. In this review, we aim to summarize how the use of novel agents that are approved for the treatment of TCLs-such as mogamulizumab, brentuximab vedotin, lenalidomide, histone deacetylase inhibitors, enhancer of zeste homolog inhibitors, and immune checkpoint inhibitors-before or after allo-HCT may impact transplantation outcomes in patients with TCLs.

摘要

与B细胞淋巴瘤相比,T细胞淋巴瘤(TCLs)的预后通常较差,符合条件的患者常考虑进行异基因造血细胞移植(allo-HCT)。多年来,TCLs疗效较差的主要原因之一是缺乏有效的新型药物,导致持续依赖传统的细胞毒性化疗方案。然而,在过去十年中,已经开发出几种对TCLs有显著疗效的新型药物。值得注意的是,其中许多药物不仅具有直接抗肿瘤作用,还能调节宿主免疫功能,这就引发了关于这些药物与allo-HCT最佳联合使用的临床问题。在这篇综述中,我们旨在总结在allo-HCT之前或之后使用已获批用于治疗TCLs的新型药物,如莫加莫拉单抗、本妥昔单抗、来那度胺、组蛋白去乙酰化酶抑制剂、EZH2抑制剂和免疫检查点抑制剂,如何影响TCLs患者的移植结局。

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