Suppr超能文献

慢性淋巴细胞白血病的 Richter 转化——我们是否取得了进展?

Richter Transformation of Chronic Lymphocytic Leukemia-Are We Making Progress?

机构信息

Division of Hematology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.

出版信息

Curr Hematol Malig Rep. 2023 Oct;18(5):144-157. doi: 10.1007/s11899-023-00701-y. Epub 2023 Jun 9.

Abstract

PURPOSE OF REVIEW

The treatment paradigm of chronic lymphocytic leukemia (CLL) has dramatically changed with the advent of novel targeted agents over the past decade. Richter transformation (RT), or the development of an aggressive lymphoma from a background of CLL, is a well-recognized complication of CLL and carries significantly poor clinical outcomes. Here, we provide an update on current diagnostics, prognostication, and contemporary treatment of RT.

RECENT FINDINGS

Several genetic, biologic, and laboratory markers have been proposed as candidate risk factors for the development of RT. Although a diagnosis of RT is typically suspected based on clinical and laboratory findings, tissue biopsy is essential for histopathologic confirmation of diagnosis. The standard of care for RT treatment at this time remains chemoimmunotherapy with the goal of proceeding to allogeneic stem cell transplantation in eligible patients. Several newer treatment modalities are being studied for use in the management of RT, including small molecules, immunotherapy, bispecific antibodies, and chimeric antigen receptor T-cell (CAR-T) therapy. The management of patients with RT remains a challenge. Ongoing trials show enormous promise for newer classes of therapy in RT, with the hope being that these agents can synergize, and perhaps supersede, the current standard of care in the near future.

摘要

目的综述

在过去十年中,随着新型靶向药物的出现,慢性淋巴细胞白血病(CLL)的治疗模式发生了巨大变化。Richter 转化(RT),即从 CLL 背景发展为侵袭性淋巴瘤,是 CLL 的一种公认并发症,临床结局极差。本文就 RT 的当前诊断、预后和现代治疗方法进行更新。

最近的发现

已提出几种遗传、生物学和实验室标志物作为 RT 发生的候选危险因素。尽管根据临床和实验室发现通常怀疑 RT 的诊断,但组织活检对于诊断的组织病理学确证至关重要。目前,RT 的治疗标准仍然是化疗免疫治疗,目标是使符合条件的患者接受异基因干细胞移植。目前正在研究几种新的治疗方法,包括小分子药物、免疫疗法、双特异性抗体和嵌合抗原受体 T 细胞(CAR-T)疗法,用于 RT 的管理。RT 患者的管理仍然是一个挑战。正在进行的试验表明,新型治疗药物在 RT 中有巨大的应用前景,希望这些药物能够协同作用,并可能在不久的将来取代目前的标准治疗。

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