Hôpital Pitié salpêtrière AP-HP, Paris, France.
PELYON, Lyon, France.
Ann Hematol. 2024 Aug;103(8):2969-2981. doi: 10.1007/s00277-024-05859-w. Epub 2024 Jul 5.
Ibrutinib is a Bruton's tyrosine kinase inhibitor indicated for the first-line treatment and relapse of chronic lymphocytic leukaemia (CLL), Waldenström's macroglobulinemia (WM) and mantle cell lymphoma (MCL). This study aimed to describe the characteristics of CLL patients treated with ibrutinib and its effectiveness, safety, and treatment pattern in real life.
All patients covered by the general health scheme (approximately 80% of the French population) with a first ibrutinib dispensation from August 1, 2017 (date of reimbursement in France) to December 31, 2020, were identified in the French National Health Insurance database (SNDS). An algorithm was developed to identify the disease (CLL, MCL or WM) for which ibrutinib was prescribed. This article focused on CLL patients. The time to next treatment (TTNT) was plotted using Kaplan‒Meier curves.
During this period, 6,083 patients initiated ibrutinib, among whom 2,771 (45.6%) patients had CLL (mean age of 74 years; 61% of men). At ibrutinib initiation, 46.6% of patients had a cardiovascular comorbidity. Most patients (91.7%) were not hospitalized during the exposure period for one of the cardiovascular or bleeding events studied. Hospitalizations were more frequent in patients with a cardiovascular comorbidity (5.9% versus 11.0%, p-value < 0.0001) and aged over 70 (5.9% versus 9.4%, p-value < 0.0001). The median TTNT was not reached.
This is one of the largest cohorts of ibrutinib-treated patients in the world. The profile of CLL patients treated with ibrutinib was in accordance with the marketing authorization and reimbursement. This study confirmed effectiveness and safety data.
伊布替尼是一种布鲁顿酪氨酸激酶抑制剂,适用于慢性淋巴细胞白血病(CLL)、华氏巨球蛋白血症(WM)和套细胞淋巴瘤(MCL)的一线治疗和复发。本研究旨在描述真实世界中接受伊布替尼治疗的 CLL 患者的特征及其有效性、安全性和治疗模式。
所有在 2017 年 8 月 1 日(法国报销日期)至 2020 年 12 月 31 日期间首次获得伊布替尼配药的覆盖全民健康保险计划(约占法国人口的 80%)的患者均在法国国家健康保险数据库(SNDS)中确定。开发了一种算法来识别开具伊布替尼的疾病(CLL、MCL 或 WM)。本文主要关注 CLL 患者。采用 Kaplan-Meier 曲线绘制至下一次治疗的时间(TTNT)。
在此期间,6083 名患者开始使用伊布替尼,其中 2771 名(45.6%)患者患有 CLL(平均年龄 74 岁;61%为男性)。在开始伊布替尼治疗时,46.6%的患者存在心血管合并症。在研究的心血管或出血事件中,大多数患者(91.7%)在暴露期间无需住院治疗。合并心血管疾病的患者(5.9%比 11.0%,p 值<0.0001)和年龄超过 70 岁的患者(5.9%比 9.4%,p 值<0.0001)的住院频率更高。中位 TTNT 未达到。
这是世界上最大的伊布替尼治疗患者队列之一。接受伊布替尼治疗的 CLL 患者的特征与上市许可和报销相符。本研究证实了有效性和安全性数据。