Allan John N, Furman Richard R
Department of Medicine, Division of Hematology & Medical Oncology, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 East 68th Street, New York, NY 10065, USA.
Int J Hematol Oncol. 2019 Jan 8;7(4):IJH09. doi: 10.2217/ijh-2018-0010. eCollection 2018 Dec.
Richter's syndrome (RS) is a life-threatening complication of chronic lymphocytic leukemia (CLL). While previous research has increased our knowledge on the distinct evolutionary patterns of RS and provided a deeper understanding of the risk factors and molecular events predisposing to transformation, there remain few targetable aberrations and treatment is largely ineffective. The ability to obtain deeper remissions, without selecting for deletion 17p, by using novel B-cell receptor (BCR) antagonists and bcl2 inhibition might lead to a decrease in the incidence of RS, but these agents have done little to significantly change outcomes when incorporated into treatment regimens for RS. In this review we highlight the current landscape of molecular lesions specific to RS, review the data on historical treatment options, and look to the horizon for potential opportunities in the future.
里氏综合征(RS)是慢性淋巴细胞白血病(CLL)的一种危及生命的并发症。虽然先前的研究增加了我们对RS独特进化模式的了解,并更深入地理解了导致转化的风险因素和分子事件,但仍存在少数可靶向的异常,且治疗大多无效。通过使用新型B细胞受体(BCR)拮抗剂和抑制bcl2来获得更深的缓解而不选择17p缺失,这可能会降低RS的发病率,但这些药物在纳入RS治疗方案时,对显著改变治疗结果作用不大。在本综述中,我们强调了RS特有的分子病变的当前情况,回顾了关于既往治疗选择的数据,并展望未来的潜在机会。