布鲁顿酪氨酸激酶抑制剂治疗慢性淋巴细胞白血病后Venetoclax巩固

IF 1.2
EJHaem Pub Date : 2025-06-25 DOI:10.1002/jha2.70085
Benjamin Heyman, Michael Choi, Thomas J. Kipps
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引用次数: 0

摘要

布鲁顿酪氨酸激酶抑制剂(BTKi)是治疗慢性淋巴细胞白血病(CLL)非常有效的药物,但可能导致长期的副作用。方法回顾性分析20例初始停用BTKi后CLL患者的venetoclax巩固情况。患者被给予单药venetoclax或联合obinutuzumab。结果89%的患者外周血微量残留病(MRD)反应最佳,为不可检出的MRD。中位随访时间为47.4个月,中位无进展生存期和下一次治疗时间均未达到。结论BTKi后Venetoclax巩固治疗是CLL患者可行的治疗策略,疗效令人鼓舞,值得进一步研究。临床试验注册:无
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Venetoclax Consolidation After Bruton Tyrosine Kinase Inhibitor Treatment for Patients With Chronic Lymphocytic Leukemia

Venetoclax Consolidation After Bruton Tyrosine Kinase Inhibitor Treatment for Patients With Chronic Lymphocytic Leukemia

Introduction

Bruton tyrosine kinase inhibitors (BTKi) are highly effective therapy for chronic lymphocytic leukemia (CLL) but can lead to long-term side effects.

Methods

We performed a retrospective analysis of venetoclax consolidation of 20 patients with CLL after initial BTKi discontinuation. Patients were administered either single-agent venetoclax or in combination with obinutuzumab.

Results

The best peripheral blood minimal residual disease (MRD) response was undetectable MRD, occurring in 89% of patients. With a median follow-up of 47.4 months, both the median progression-free survival and time-to-next treatment were not reached.

Conclusion

Venetoclax consolidation after BTKi is a feasible treatment strategy for patients with CLL, with encouraging efficacy deserving further study.

Clinical Trial Registration: N/A

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