[Real-life evaluation of the care pathway of patients eligible for axicabtagene ciloleucel treatment: Analysis of a multicenter retrospective cohort (IMPA-CT study)].

Guillaume Cartron, Catherine Thieblemont, Isabelle Borget, Catherine Rioufol, Margaux Berthet, Camille Portal, Clémentine Baujat, Enora Alaoui, Sandrine Baffert, Damien Lacroix, Pierre Bories, Ibrahim Yakoub-Agha, Roch Houot
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Abstract

The arrival of CAR-T cell treatments in Europe in 2018 has considerably changed the clinical and logistical management of lymphoma patients. The aim of this study is to evaluate pathways of patients eligible for axicabtagene ciloleucel (axi-cel), particularly previously and afterwards of its administration, stages that are currently poorly documented in the literature. Ninety-eight patients from eleven French qualified centers eligible for axi-cel treatment between June 2020 and February 2021 were retrospectively included. Of all the stages in the care pathway evaluated, the median time observed between relapse after the previous line and prescription of axi-cel was 27days, and the median time between the multidisciplinary consultation meeting and axi-cel administration was 63days. The two main methods of discharge from hospital were a return home (65% of cases) or hospitalisation in a rehabilitation unit (20% of cases). Among all the geographical and organizational characteristics assessed, no factor was found to have a significant impact on the time length of the patient's journey, apart from the patient capacity of the qualified center, and the origin of the patient's referral (coming from a qualified or a referral center). Since the study was carried out, the number of qualified centers has continued to rise, improving territorial coverage and access to treatment.

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[对符合阿昔单抗西乐葆治疗条件的患者的护理路径进行真实评估:多中心回顾性队列分析(IMPA-CT 研究)]。
2018年,CAR-T细胞疗法登陆欧洲,大大改变了淋巴瘤患者的临床和后勤管理。本研究旨在评估符合axicabtagene ciloleucel(axi-cel)治疗条件的患者的治疗路径,尤其是用药前和用药后,这些阶段目前在文献中记载较少。研究人员回顾性地纳入了来自法国11家合格中心的98名患者,这些患者均符合在2020年6月至2021年2月期间接受axi-cel治疗的条件。在评估的治疗路径的所有阶段中,观察到上一疗程后复发与开具阿昔洛韦处方之间的中位时间为27天,多学科会诊会议与阿昔洛韦用药之间的中位时间为63天。出院的两种主要方式是回家(65%的病例)或在康复科住院(20%的病例)。在评估的所有地理和组织特征中,除了合格中心的病人容量和病人的转诊来源(来自合格中心或转诊中心)外,没有发现其他因素对病人的旅程时间长度有显著影响。自这项研究开展以来,合格中心的数量不断增加,提高了地区覆盖率和获得治疗的机会。
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