研究概要
Tisa-cel 在重度经治 FL 中已显示出高缓解率和持久缓解,并具有良好安全性特征,包括 POD24 等高危人群。
中文摘要
引言:滤泡性淋巴瘤(FL)是一种惰性但无法治愈的非霍奇金淋巴瘤亚型,特点是反复复发,且每增加一线治疗,应答逐渐减弱。尽管一线化学免疫治疗初始缓解率较高,部分患者——尤其是早期复发者(POD24)——结局较差,需要替代疗法。靶向CD19的嵌合抗原受体(CAR)T细胞疗法替沙仑赛(tisa-cel)已成为复发/难治性(r/r)FL的一种有前景选择,有望带来深度、持久缓解。综述内容:本文介绍tisa-cel的科学依据、临床前创新和临床开发历程,从第二代CAR-T 工程化起源到其在血液系统恶性肿瘤中的关键性试验。综述基于PubMed、Embase及主要血液学会议摘要的文献检索,时间范围为1987年至2025年4月,详细介绍ELARA试验结果、后续长期及真实世界数据,以及r/r FL三线治疗的竞争格局。专家观点:tisa-cel在经多线治疗的FL患者(包括POD24等高危人群)中表现出较高缓解率、持续缓解和良好安全性。双特异性抗体便于门诊给药,而CAR-T 可能实现深度且持久的缓解。tisa-cel和利基仑赛所采用的4-1BB共刺激结构域,与CD28型构建体相比,重度CRS和ICANS发生率较低。随着领域发展,谨慎筛选患者并开展头对头试验,对于优化r/r FL治疗顺序至关重要。
展开英文摘要原文
INTRODUCTION: Follicular lymphoma (FL) is an indolent yet incurable subtype of non-Hodgkin lymphoma characterized by repeated relapses and diminishing responses with each treatment line. Although front-line chemoimmunotherapy achieves high initial response rates, a subset of patients - particularly those with early relapse (POD24) - experience poor outcomes and require alternative therapies. Tisagenlecleucel (tisa-cel), a CD19-directed chimeric antigen receptor (CAR) T-cell therapy, has emerged as a promising option for relapsed or refractory (r/r) FL, offering the potential for deep and durable remissions. AREAS COVERED: This review covers the scientific rationale, preclinical innovations, and clinical development of tisa-cel, from its origins in 2 nd -generation CAR-T engineering to its pivotal trials in hematologic malignancies.
It is based on a literature search using PubMed, Embase, and conference abstracts from major hematology meetings from 1987 to April 2025. The paper deta ils the ELARA trial outcomes, subsequent long-term and real-world data, and the competitive landscape of third-line therapies for r/r FL. EXPERT OPINION: Tisa-cel has demonstrated high response rates and sustained remissions with a favorable safety profile in heavily pretreated FL, including high-risk populations such as those with POD24.
While bispecific antibodies offer convenient outpatient administration, CAR-T cell therapy provides the potential for deep and durable remissions. The 4-1BB costimulatory domain used in tisa-cel and liso-cel is associated with a lower incidence of severe CRS and ICANS compared to CD28-based constructs. the field evolves, careful patient selection and head-to-head trials will be essential to refine therapeutic sequencing in r/r FL.
论文信息
- 作者
- Kungwankiattichai S、Maziarz RT
- 单位
- Center for Hematologic Malignancies, Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.United States
- 文献类型
- 综述
- 期刊
- Expert opinion on drug discovery2025 Nov