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慢性淋巴细胞白血病Richter转化的分子遗传学与治疗进展

Advances in the understanding of molecular genetics and therapy of Richter transformation in chronic lymphocytic leukemia.

作者信息

Deodato Marina, Frustaci Anna Maria, Zappaterra Arianna, Rapella Alberto, Gambacorti-Passerini Carlo, Cairoli Roberto, Montillo Marco, Tedeschi Alessandra

机构信息

Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Department of Hematology and Bone Marrow Transplantation Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

出版信息

Leuk Lymphoma. 2024 Dec;65(14):2096-2107. doi: 10.1080/10428194.2024.2398660. Epub 2024 Sep 2.

DOI:10.1080/10428194.2024.2398660
PMID:39219481
Abstract

Richter's transformation (RT) is defined as the evolution of chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) into an aggressive lymphoma, most commonly diffuse large B-cell lymphoma. This complication is rare and aggressive, with poor prognosis and dismal survival. Clonal relationship with the underlying CLL/SLL, observed in ∼80% of cases, represents one of the main factors affecting prognosis. Treatment has been historically based on chemoimmunotherapy, but frequent mutations in genes involved in cell survival and proliferation-such as TP53, NOTCH1, MYC, CDKN2A-confer resistance to standard treatments. During the last years, advances in the knowledge of the biological mechanisms underlying RT allowed to identify genetic and molecular lesions that can potentially be targeted by novel selective agents. Pathway and checkpoint inhibitors, bispecific antibodies and CAR T-cell therapy are currently under investigation and represent promising treatment options. This review summarizes current biological evidence and available data on novel therapeutic agents.

摘要

里氏转化(RT)被定义为慢性淋巴细胞白血病(CLL)或小淋巴细胞淋巴瘤(SLL)演变为侵袭性淋巴瘤,最常见的是弥漫性大B细胞淋巴瘤。这种并发症罕见且具有侵袭性,预后不良,生存率极低。在约80%的病例中观察到与潜在的CLL/SLL存在克隆关系,这是影响预后的主要因素之一。历史上,治疗一直基于化疗免疫疗法,但参与细胞存活和增殖的基因(如TP53、NOTCH1、MYC、CDKN2A)频繁发生突变,导致对标准治疗产生耐药性。在过去几年中,对RT潜在生物学机制的认识取得了进展,从而能够识别可能被新型选择性药物靶向的基因和分子损伤。通路和检查点抑制剂、双特异性抗体以及嵌合抗原受体(CAR)T细胞疗法目前正在研究中,是很有前景的治疗选择。本综述总结了当前的生物学证据以及关于新型治疗药物的现有数据。

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