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美国接受共价 BTK 和 BCL2 抑制剂治疗的慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤(SLL)患者的临床结局:真实世界数据库研究。

Clinical outcomes among patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) who received treatment with a covalent BTK and BCL2 inhibitor in the United States: a real-world database study.

机构信息

Oxford Cancer and Hematology Centre, Oxford University NHS Foundation Trust, Oxford, UK.

Eli Lilly and Company, Indianapolis, IN, USA.

出版信息

Leuk Lymphoma. 2023 May;64(5):1005-1016. doi: 10.1080/10428194.2023.2190436. Epub 2023 Mar 29.

Abstract

This retrospective study using the nationwide de-identified Flatiron Health electronic health record-derived database was designed to evaluate clinical outcomes among patients with chronic lymphocytic leukemia (CLL) who previously received both a covalent Bruton's tyrosine kinase inhibitor (cBTKi) and B-cell lymphoma 2 inhibitor (BCL2i) in a real-world setting. Outcomes for the immediate next line of therapy following the latter of the cBTKi or BCL2i treatment included: real-world response rate of 34.4% (using methods most consistent with clinical trials); median duration of real-world response of 13.3 months; and median real-world progression-free survival of 9.2 months. Median overall survival was 25.5 months from the start of the immediate next line of therapy. There remains a need for more effective therapies after cBTKi and BCL2i therapy for patients with CLL.

摘要

本回顾性研究利用全国范围内去识别化的 Flatiron Health 电子健康记录数据库,旨在评估在真实环境中接受过共价布鲁顿酪氨酸激酶抑制剂 (cBTKi) 和 B 细胞淋巴瘤 2 抑制剂 (BCL2i) 治疗的慢性淋巴细胞白血病 (CLL) 患者的临床结局。在接受后者治疗后,紧接着的下一线治疗的结局包括:真实世界的反应率为 34.4%(使用与临床试验最一致的方法);真实世界反应的中位持续时间为 13.3 个月;真实世界无进展生存期的中位时间为 9.2 个月。从紧接着的下一线治疗开始,中位总生存期为 25.5 个月。对于接受过 cBTKi 和 BCL2i 治疗的 CLL 患者,仍需要更有效的治疗方法。

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