德国慢性淋巴细胞白血病治疗的十年:真实世界的治疗模式和结果(2010-2022 年)

EJHaem Pub Date : 2024-04-05 DOI:10.1002/jha2.888
Hannes Wartmann, Anna Kabilka, Barthold Deiters, Norbert Schmitz, Timm Volmer
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引用次数: 0

摘要

近年来,慢性淋巴细胞白血病(CLL)的药物治疗方案大幅增加。这些选择包括化疗、化学免疫疗法和信号通路抑制剂。随着 2016 年伊布替尼(ibrutinib)的广泛应用,治疗格局开始发生显著变化。本次理赔数据分析的重点是了解过去十年间德国临床实践中新型疗法的使用情况。研究使用了德国法定医疗保险的匿名理赔数据(2010-2022 年),涵盖了患者的人口统计学特征、治疗方法和处方。研究对象包括两次确诊为 CLL 的患者。研究人员对治疗模式进行了分析,并使用时间到事件分析法对生存结果进行了比较。在分析的2983名CLL患者中,有1041人在2011年至2022年期间开始接受一线治疗,从确诊到首次处方的中位时间为18个月。化学免疫疗法在2019年之前一直是最主要的一线疗法,但现在已明显减少,而靶向疗法的使用率则从2015年的3%增至2022年的77%。2016年后,靶向疗法在接受复发或难治性疾病治疗的患者中占据主导地位。中位治疗持续时间分别为化疗 122 天,化疗免疫 176 天,靶向治疗 373 天。2016年或之后确诊的患者总生存率明显更高(危险比为0.56,95%置信区间为0.44-0.69)。伊布替尼和 venetoclax 等靶向疗法的采用改变了德国的 CLL 治疗,改善了患者的预后。此外,我们还展示了对不断发展的临床指南的成功遵循。
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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A decade of chronic lymphocytic leukaemia therapy in Germany: Real-world treatment patterns and outcomes (2010–2022)

Pharmacotherapy options for chronic lymphocytic leukaemia (CLL) have expanded significantly in recent years. These options include chemotherapy, chemoimmunotherapy and signalling pathway inhibitors. A notable shift in the treatment landscape began with the widespread adoption of ibrutinib in 2016. This analysis of claims data focuses on understanding how the use of novel therapies has evolved in clinical practice over the past decade in Germany. Anonymized claims data (2010–2022) from German statutory health insurance was used, covering patient demographics, treatments, and prescriptions. The study population included patients with two confirmed CLL diagnoses. Treatment patterns were analysed, and survival outcomes were compared using time-to-event analyses. In the analysed cohort of 2983 incident CLL patients, 1041 started first-line therapy between 2011 and 2022, with a median duration of 18 months from diagnosis to the first prescription. Chemoimmunotherapy, the predominant 1L therapy until 2019, decreased significantly, while targeted therapy usage increased from 3% in 2015 to 77% in 2022. Targeted therapies became dominant in patients receiving treatment for relapsed or refractory disease after 2016. Median treatment durations were: 122 days for chemo, 176 days for chemo-immuno, and 373 days for targeted therapy. The overall survival for patients diagnosed in or after 2016 was significantly better (hazard ratio 0.56, 95% confidence interval, 0.44–0.69)). The adoption of targeted therapies like ibrutinib and venetoclax has transformed CLL treatment in Germany, leading to improved patient outcomes. Additionally, we demonstrate successful adherence to evolving clinical guidelines.

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