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Richter 转化:生物学见解、诊断挑战与新兴疗法

英文原题:Richter transformation: biological insights, diagnostic challenges and emerging therapies.

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Richter transformation: biological insights, diagnostic challenges and emerging therapies.

PubMed 2025/07/04(内容时间) Curr Opin Oncol Q3 · IF 2.4(JCR 2025)

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研究思路按摘要原文分段

本综述旨在强调Richter转化(RT)相关进展日益增多的重要意义,RT是一种侵袭性淋巴瘤,发生于慢性淋巴细胞白血病(CLL)或小淋巴细胞淋巴瘤患者。

测序分析工具和单细胞方法的发展克服了RT中细胞混合的主要挑战,使人们能够更深入地理解驱动CLL向RT转化的基因改变。这些技术还使得在临床发病前很久就能检测到RT克隆。与此同时,针对CLL的新型靶向治疗和针对淋巴瘤的免疫治疗策略正带来新的希望。近期2期研究尤其支持免疫检查点抑制剂和双特异性T细胞衔接器在RT中的潜在作用,而CAR-T 细胞疗法的经验也在不断积累,为改善这一历史上难以治疗疾病的结局带来了希望。总结:近期研究正聚焦于更好地理解转化过程、改善RT的早期检测,以及为RT患者开发新型靶向和免疫治疗及联合方案。

展开英文摘要原文

PURPOSE OF REVIEW: this review aims to underscore the significance of the growing number of advances related to Richter transformation (RT), an aggressive form of lymphoma arising in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma. RECENT FINDINGS: The development of sequencing analytic tools and single-cell approaches has overcome the major challenge of cellular admixture in RT, enabling a deeper understanding of the genetic alterations driving transformation from CLL to RT. These techniques have also made it possible to detect RT clones long before clinical onset.

In parallel, novel targeted therapies for CLL and immunotherapeutic strategies for lymphomas are offering renewed hope. Recent phase 2 studies notably support the potential role of immune checkpoint inhibitors and bispecific T-cell engagers in RT, while experience with chimeric antigen receptor T-cell therapies continues to grow, raising hopes for improved outcomes in this historically difficult-to-treat condition.

SUMMARY: recent research is focusing on better understanding the transformation process, improving the early detection of RT, and developing novel targeted and immunotherapy treatments and combinations for patients with RT.

论文信息

作者
Guièze R
单位
CHU Clermont-Ferrand, Service de Thérapie Cellulaire et d'Hématologie Clinique.
文献类型
综述
期刊
Current opinion in oncology2025 Sep 1
原文标识
PubMed 40621821 · DOI 10.1097/CCO.0000000000001173