An experience with ibrutinib monotherapy for Richter's syndrome isolated in the central nervous system.

IF 0.9 Q4 HEMATOLOGY
Yuma Nato, Keiki Nagaharu, Kanako Inoue, Kodai Yabu, Akihiko Sawaki, Takuya Shiotani, Yuki Kageyama, Ken Tanaka, Koichi Ohshima, Hiroyuki Miyashita
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引用次数: 1

Abstract

Richter's syndrome (RS) of the central nervous system (CNS) is known to have an extremely poor prognosis. Ibrutinib has been reported to have some activity in patients with RS, despite its poor prognosis. Although ibrutinib crosses the blood-brain barrier, its efficacy in RS patients with CNS involvement remains unknown. Here, we report a case of RS isolated in the CNS that was confirmed to be clonally related to chronic lymphocytic leukemia (CLL) by immunoglobulin heavy chain gene analysis. Although the median survival of patients with RS clonally related to CLL was significantly shorter than that of patients with RS clonally unrelated to CLL, the patient received ibrutinib monotherapy without experiencing any significant adverse events, and the disease remained stable with ibrutinib until 6 weeks later. Following whole-brain radiation therapy (40 Gy in 20 fractions) with dexamethasone, the patient has survived for five months after diagnosis. Thus, ibrutinib may be a safe and effective therapeutic option for patients with RS and CNS involvement.

伊鲁替尼单药治疗中枢神经系统孤立的里希特综合征的经验。
中枢神经系统(CNS)的里希特综合征(RS)已知预后极差。据报道,伊鲁替尼在RS患者中有一定的活性,尽管预后较差。尽管伊鲁替尼能穿过血脑屏障,但其对累及中枢神经系统的RS患者的疗效尚不清楚。在此,我们报告一例分离于中枢神经系统的RS,经免疫球蛋白重链基因分析证实与慢性淋巴细胞白血病(CLL)克隆相关。虽然与CLL克隆相关的RS患者的中位生存期明显短于与CLL克隆无关的RS患者,但该患者接受伊鲁替尼单药治疗后未发生任何明显不良事件,并且伊鲁替尼治疗后病情保持稳定,直至6周后。在用地塞米松进行全脑放射治疗(40 Gy,分20次)后,患者在诊断后存活了5个月。因此,依鲁替尼可能是RS和CNS受累患者安全有效的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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