Efficacy and Safety of Experimental versus Approved CAR T-cell Therapies in Large B-cell Lymphoma Using Matching Adjusted Indirect Comparisons: A Systematic Review and Meta-Analysis Protocol

Bayarmagnai Munkhjargal, B. Muresan, S. Solano, A. Macedo, Yoonjung Lee, Gwang-Jin Kim, C. Camargo, Yeseul Ahn, D. Carpenter, Yuchen Su, Gabriela M. Henriquez Luthje
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引用次数: 1

Abstract

Background: Relapsed and refractory large B cell lymphomas (RR-LBCL) have a poor prognosis. Chimeric antigen receptor (CAR) T-cell therapies have shown considerably high response rates even in RR-LBCL patients who fail to achieve remission after multiple chemotherapy lines. Currently, three CAR T-cell treatments axicabtagene ciloleucel (Yescarta), tisagenlecleucel (Kymriah), and lisocabtagene maraleucel (Breyanzi) have been approved for adults with RR-LBCL by regulatory agencies. Non-pivotal clinical trials have independently examined different types of CAR T-cells and have demonstrated remarkable clinical benefit and safety. Yet, no comparison of the experimental and approved CAR T-cells
使用匹配调整间接比较的实验性与批准的CAR - t细胞疗法治疗大b细胞淋巴瘤的疗效和安全性:一项系统评价和荟萃分析方案
背景:复发性和难治性大B细胞淋巴瘤(RR-LBCL)预后不良。嵌合抗原受体(CAR)T细胞疗法显示出相当高的应答率,即使在RR-LBCL患者中,这些患者在多种化疗后未能获得缓解。目前,监管机构已批准三种CAR T细胞治疗方法axicabtane cilloucel(Yescarta)、tisagenlecleucel(Kymriah)和lisocabtagene maraleucel(Breyanzi)用于成人RR-LBCL。非关键临床试验独立检测了不同类型的CAR T细胞,并证明了显著的临床益处和安全性。然而,实验和批准的CAR T细胞没有比较
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