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克服复发/难治性弥漫大 B 细胞淋巴瘤患者转诊 CAR-T 细胞治疗的障碍

英文原题:Overcoming Barriers to Referral for Chimeric Antigen Receptor T Cell Therapy in Patients with Relapsed/Refractory Diffuse Large B Cell Lymphoma.

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Overcoming Barriers to Referral for Chimeric Antigen Receptor T Cell Therapy in Patients with Relapsed/Refractory Diffuse Large B Cell Lymphoma.

PubMed 2023/04/07(内容时间) Transplant Cell Ther Q1 · IF 4.7(JCR 2025)

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中文摘要

弥漫大B细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤亚型。尽管一线治疗效果令人鼓舞,对一线治疗难治或复发患者预后较差;SCHOLAR-1研究显示,许多患者接受更多线细胞毒化疗后仍死于疾病。CAR-T 通过重编程患者自身T细胞来识别和清除癌细胞,最初获FDA批准用于复发/难治性DLBCL三线治疗。根据近期随机研究,阿基仑赛和利基仑赛也获准作为原发难治或一线治疗后12个月内复发患者的二线治疗。虽然CD19 CAR-T 疗效确立,但符合条件患者仍可能无法接受治疗,障碍包括费用、患者顾虑、需前往学术中心、未获转诊、认知不足、照护者支持缺乏、资源信息不足,以及转诊肿瘤医生未能及时筛选。本综述概述获批的tisagenlecleucel、axicabtagene ciloleucel和lisocabtagene maraleucel关键试验及真实世界证据;两种情境均显示安全有效,但患者可及性仍受多重障碍限制。文中介绍转诊障碍,并提出促进社区肿瘤医生与CAR-T 中心合作及患者后续社区长期管理的建议。

展开英文摘要原文

Diffuse large B cell lymphoma (DLBCL) is the most prevalent subtype of non-Hodgkin lymphoma. Although outcomes to frontline therapy are encouraging, patients who are refractory to or in relapse after first-line therapy experience inferior outcomes. A significant proportion of patients treated with additional lines of cytotoxic chemotherapy ultimately succumb to their disease, as established in the SCHOLAR-1 study. Chimeric antigen receptor (CAR) T cell therapy is a novel approach to cancer management that reprograms a patient's own T cells to better target and eliminate cancer cells. It was initially approved by the US Food and Drug Administration for patients with relapsed/refractory (r/r) DLBCL as a third line of treatment. Based on recently published randomized data, CAR-T therapy (axicabtagene ciloleucel and lisocabtagene maraleucel) also has been approved as a second line of treatment for patients who are primary refractory or relapse within 12 months of first-line therapy. Despite the proven efficacy in treating r/r DLBCL with CD19-directed CAR-T therapy, several barriers may prevent eligible patients from receiving treatment.

Barriers to CAR-T therapy include cost of therapy, patient hesitancy, required travel to academic treatment centers, nonreferrals, poor understanding of CAR-T therapy, lack of caregiver support, knowledge of available resources, and timely patient selection by referring oncologists. In this review, we provide an overview of the FDA-approved CD19-directed CAR-T cell therapies (tisagenlecleucel, axicabtagene ciloleucel, and lisocabtagene maraleucel) from pivotal clinical trials and supporting real-world evidence from retrospective studies.

In both clinical trials and real-world settings, CAR-T therapy has been shown to be safe and efficacious for treating patients with r/r DLBCL: however, several barriers prevent eligible patients from accessing these therapies. Barriers to referrals for CAR-T therapy are described, along with recommendations to improve collaboration between community oncologists and physicians from CAR-T therapy treatment centers and subsequent long-term care of patients in community treatment centers.

论文信息

作者
Hoffmann MS、Hunter BD、Cobb PW、Varela JC、Munoz J
单位
University of Kansas Cancer Center, Division of Hematologic Malignancies and Cellular Therapeutics, Westwood, Kansas. Electronic address: mhoffmann@kumc.edu.
文献类型
综述 · 非美国政府资助研究
期刊
Transplantation and cellular therapy2023 Jul
原文标识
PubMed 37031747 · DOI 10.1016/j.jtct.2023.04.003