Lifileucel: First Approval

IF 4.1 3区 医学 Q1 GENETICS & HEREDITY
Susan J. Keam
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引用次数: 0

Abstract

Lifileucel (AMTAGVI™), a one-time autologous T cell therapy derived and expanded from tumour-infiltrating lymphocytes (TIL) from a patient’s own tumour, is being developed by Iovance Biotherapeutics, Inc. for the treatment of cancer. Lifileucel was granted accelerated approval based on objective response rate (ORR) in February 2024 in the USA for use in adult patients with unresectable or metastatic melanoma previously treated with a PD-1 blocking antibody, and if BRAF V600 mutation positive, a BRAF inhibitor with or without a MEK inhibitor. This article summarizes the milestones in the development of lifileucel leading to this first approval for the treatment of patients with unresectable or metastatic melanoma who have progressed on or after prior anti-PD-1/L1 therapy and targeted therapy.

Lifileucel:首次批准
Lifileucel(AMTAGVI™)是一种一次性自体T细胞疗法,由来自患者自身肿瘤的肿瘤浸润淋巴细胞(TIL)衍生和扩增而来,由Iovance生物治疗公司开发,用于治疗癌症。Lifileucel 于 2024 年 2 月在美国获得基于客观反应率 (ORR) 的加速批准,用于既往接受过 PD-1 阻断抗体治疗的不可切除性或转移性黑色素瘤成人患者,如果 BRAF V600 突变阳性,则用于 BRAF 抑制剂联合或不联合 MEK 抑制剂的治疗。本文总结了lifileucel开发过程中的里程碑事件,这也是lifileucel首次获批用于治疗既往接受过抗PD-1/L1治疗和靶向治疗后病情进展的不可切除或转移性黑色素瘤患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.50%
发文量
53
审稿时长
>12 weeks
期刊介绍: Molecular Diagnosis & Therapy welcomes current opinion articles on emerging or contentious issues, comprehensive narrative reviews, systematic reviews (as outlined by the PRISMA statement), original research articles (including short communications) and letters to the editor. All manuscripts are subject to peer review by international experts.
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