FIRE Study: Real-World Effectiveness and Safety of Ibrutinib in Clinical Practice in Patients with CLL and MCL.

Clinical Hematology International Pub Date : 2022-09-01 Epub Date: 2022-09-14 DOI:10.1007/s44228-022-00015-5
Caroline Dartigeas, Borhane Slama, Margaret Doyle, Christoph Tapprich, Claire Albrecht, Sandrine Dupuis, Robert Wapenaar, Charlotte Schmidt-Hieber, Veronique Leblond
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引用次数: 2

Abstract

The FIRE study investigated the real-world effectiveness and safety of ibrutinib in prospectively observed patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) and mantle cell lymphoma (MCL) in France. Patients were mostly relapsed/refractory with high-risk features. First-line CLL/SLL patients had del17p and/or TP53 mutations. In this interim analysis, the median follow-up time for patients with CLL/SLL and MCL was 17.7 and 15.1 months, respectively. In the effectiveness populations for CLL/SLL (n = 200) and MCL (n = 59), the median progression-free survival was not estimable and 12.4 months, respectively; the 12-month overall survival rates were 88.5% and 65.8%, respectively. Treatment-emergent adverse events of interest for patients with CLL/SLL (n = 202) and MCL (n = 59) included: infections and infestations (53.5% and 32.2%), major bleeding (5.0% and 5.1%), and atrial fibrillation (5.9% and 8.5%); 135 (66.8%) and 20 (33.9%) patients were continuing treatment at the time of data cutoff. Future analyses will report on longer-term follow-up (Trial registration: ClinicalTrials.gov, NCT03425591. Registered 1 February 2018-Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT03425591 ).

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FIRE研究:伊鲁替尼在CLL和MCL患者临床实践中的有效性和安全性。
FIRE研究调查了伊鲁替尼在法国对慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤(SLL)和套细胞淋巴瘤(MCL)的前瞻性观察患者的实际有效性和安全性。患者多为复发/难治性高危患者。一线CLL/SLL患者有del17p和/或TP53突变。在这项中期分析中,CLL/SLL和MCL患者的中位随访时间分别为17.7个月和15.1个月。在CLL/SLL (n = 200)和MCL (n = 59)的有效人群中,中位无进展生存期分别为12.4个月和不可估计;12个月总生存率分别为88.5%和65.8%。CLL/SLL (n = 202)和MCL (n = 59)患者在治疗中出现的不良事件包括:感染和感染(53.5%和32.2%)、大出血(5.0%和5.1%)和房颤(5.9%和8.5%);截至数据截止时,135例(66.8%)和20例(33.9%)患者仍在继续治疗。未来的分析将报告长期随访(试验注册:ClinicalTrials.gov, NCT03425591)。2018年2月1日注册-回顾性注册,https://clinicaltrials.gov/ct2/show/NCT03425591)。
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