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复发/难治性B细胞前体急性淋巴细胞白血病中CD19靶向免疫治疗后CD19阴性复发的发生率:一项综述

Incidence of CD19-negative relapse after CD19-targeted immunotherapy in R/R BCP acute lymphoblastic leukemia: a review.

作者信息

Locatelli Franco, Shah Bijal, Thomas Tracy, Velasco Kelly, Adedokun Babatunde, Aldoss Ibrahim, Gore Lia, Hoelzer Dieter, Bassan Renato, Park Jae H, Boissel Nicolas, Kantarjian Hagop

机构信息

Department of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children's Hospital, Catholic University of the Sacred Heart, Rome, Italy.

Moffitt Cancer Center, Tampa, Florida, USA.

出版信息

Leuk Lymphoma. 2023 Oct;64(10):1615-1633. doi: 10.1080/10428194.2023.2232496. Epub 2023 Aug 1.

Abstract

There are inconsistencies in the reporting of CD19 antigen status following treatment with CD19-targeted therapies. A majority of evidence comes from studies reporting small sample sizes. In this review, we systematically summarize published studies that have reported rates of CD19-negative relapse after treatment with either blinatumomab or CD19-directed CAR T-cell therapy and report the rates of CD19-negative relapse when evaluated in a standardized way across trials. CD19-negative relapse appears to occur more commonly in relapses following CAR T-cell therapy compared with blinatumomab, whether proportions are calculated among all treated patients (8.7% vs 4.5%) or among patients who relapse (30% vs 22.5%). The median (range) duration of follow-up was 29.3 (17.4-50.8) and 20.4 (6.9-49.0) months for publications on blinatumomab ( = 10) and CAR T-cell therapies ( = 23), respectively. There is a need for standardized reporting of CD19 antigen status in the setting of relapse following novel immunotherapies to inform clinical practice.

摘要

在接受CD19靶向治疗后,CD19抗原状态的报告存在不一致性。大部分证据来自样本量较小的研究报告。在本综述中,我们系统地总结了已发表的研究,这些研究报告了使用blinatumomab或CD19导向的CAR T细胞疗法治疗后CD19阴性复发率,并报告了在各试验中以标准化方式评估时的CD19阴性复发率。与blinatumomab相比,CD19阴性复发似乎在CAR T细胞治疗后的复发中更常见,无论是在所有接受治疗的患者中计算比例(8.7%对4.5%)还是在复发患者中计算比例(30%对22.5%)。关于blinatumomab(n = 10)和CAR T细胞疗法(n = 23)的出版物,随访的中位(范围)持续时间分别为29.3(17.4 - 50.8)个月和20.4(6.9 - 49.0)个月。在新型免疫疗法后的复发情况下,需要对CD19抗原状态进行标准化报告,以为临床实践提供信息。

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