CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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.
Overcoming Barriers to Referral for Chimeric Antigen Receptor T Cell Therapy in Patients with Relapsed/Refractory Diffuse Large B Cell Lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
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。
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.
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