Outcomes among Patients with Mantle Cell Lymphoma Post-Covalent BTK Inhibitor Therapy in the United States: A Real-World Electronic Medical Records Study.

Q3 Medicine
Lisa M Hess, Yongmei Chen, Paolo B Abada, Heiko Konig, Richard A Walgren
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引用次数: 0

Abstract

Purpose: There remains a lack of consensus among experts regarding the optimal therapeutic approach for Mantle cell lymphoma (MCL) after failure of covalent Bruton Tyrosine Kinase inhibitor (cBTKi)-based therapy. This study was designed to examine patient characteristics, current treatment patterns, and clinical outcomes using a real-world database to evaluate how MCL is currently managed post-cBTKi therapy in the U.S.

Methods: A large, deidentified U.S. electronic medical record (EMR) oncology database (ConcertAI) with data from January 2011 to July 2021 was utilized for this study. Eligible patients were adults with MCL who had received at least one cBTKi. Descriptive statistics were used to evaluate patient characteristics and treatment patterns. Time-to-event real-world outcomes of duration of therapy, time to next treatment discontinuation, and overall survival was evaluated using the Kaplan-Meier method.

Results: A total of 946 patients met eligibility criteria. Of these, 739 (78.1%) discontinued cBTKi treatment before the end of the follow-up period, while the remaining 207 (21.9%) were still receiving cBTKi therapy at the end of the follow-up period. Among those who had discontinued the cBTKi, 352 (47.6%, 352/739) received at least one subsequent (post-cBTKi) treatment. The median duration of the immediate post-cBTKi therapy was 2.6 months (n = 352). Among the 739 patients who discontinued cBTKi treatment, the median time from cBTKi discontinuation to next treatment discontinuation or death was 3.9 months and the median overall survival was 10.3 months.

Conclusions: This study demonstrates the poor outcomes experienced by patients after cBTKi therapy. There is an urgent need for safe and effective treatments for patients with recurrent or progressive MCL.

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美国套细胞淋巴瘤患者共价BTK抑制剂治疗后的结果:一项真实世界电子医疗记录研究
目的:在以共价布鲁顿酪氨酸激酶抑制剂(cBTKi)为基础的治疗失败后,对于套细胞淋巴瘤(MCL)的最佳治疗方法,专家们仍然缺乏共识。本研究旨在使用真实世界数据库检查患者特征、当前治疗模式和临床结果,以评估目前在美国cbtki治疗后MCL的管理情况。方法:本研究使用了2011年1月至2021年7月的大型美国电子病历(EMR)肿瘤学数据库(ConcertAI)。符合条件的患者是接受过至少一次cBTKi治疗的成年MCL患者。描述性统计用于评估患者特征和治疗模式。使用Kaplan-Meier方法评估治疗持续时间、下次停止治疗的时间和总生存期。结果:946例患者符合入选标准。其中,739人(78.1%)在随访结束前停止了cBTKi治疗,而其余207人(21.9%)在随访结束时仍在接受cBTKi治疗。在停用cBTKi的患者中,352例(47.6%,352/739)接受了至少一次后续(cBTKi后)治疗。cbtki治疗后的中位持续时间为2.6个月(n = 352)。在停用cBTKi治疗的739例患者中,从停用cBTKi到下次停止治疗或死亡的中位时间为3.9个月,中位总生存期为10.3个月。结论:本研究表明cBTKi治疗后患者的预后较差。对于复发性或进行性MCL患者,迫切需要安全有效的治疗方法。
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
Advances in Hematology
Advances in Hematology Medicine-Hematology
CiteScore
3.30
自引率
0.00%
发文量
10
审稿时长
15 weeks
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