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CAR-T 细胞治疗在弥漫大 B 细胞淋巴瘤二线治疗中的作用

英文原题:The role of CAR-T cell therapy as second line in diffuse large B-cell lymphoma.

查看英文原题

The role of CAR-T cell therapy as second line in diffuse large B-cell lymphoma.

PubMed 2022/12/06(内容时间) Ther Adv Hematol Q2 · IF 2.8(JCR 2025)

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中文摘要

近三十年来,自体造血细胞移植(auto-HCT)一直是前线治疗后复发/难治性(R/R)弥漫性大B细胞淋巴瘤(DLBCL)患者的标准治疗。由于化疗强度大以及auto-HCT后复发患者比例较高,该方法受到限制。自抗CD19CAR-T 细胞疗法及新型药物获批以来,DLBCL的治疗格局发生了显著变化。抗CD19 CAR-T 疗法最初获批用于既往接受过两线或以上治疗的复发DLBCL,可产生持久缓解,5年随访时超过50%的患者仍存活。在此,我们讨论近期使用axicabtagene ciloleucel、tisagenlecleucel和lisocabtagene maraleucel的随机3期临床试验,这些试验在二线治疗背景下与标准治疗进行比较,研究对象为完成化学免疫治疗后12个月内出现R/R DLBCL且适合移植的患者,可能改变DLBCL的治疗算法。

展开英文摘要原文

For approximately three decades, autologous hematopoietic cell transplantation (auto-HCT) has been the standard of care for patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) after frontline therapy. This approach is limited due to the intensity of chemotherapy and the proportion of patients who relapse after auto-HCT.

Since the approval of anti-CD19 chimeric antigen receptor T-cell (CAR-T) therapy and novel agents, the treatment paradigm for DLBCL has changed remarkably. Anti-CD19 CAR-T therapy was first approved for relapsed DLBCL after two or more previous lines of therapy with long-lasting responses, with over 50% of patients still alive at 5-year follow-up.

Here, we discuss recent randomized phase 3 clinical trials using axicabtagene ciloleucel, tisagenlecleucel, and lisocabtagene maraleucel in the second-line therapy setting compared with the standard of care in transplant-eligible patients who have DLBCL R/R within 12 months of completing chemo-immunotherapy, potentially changing the treatment algorithm for DLBCL.

论文信息

作者
Albanyan O、Chavez J、Munoz J
第一作者单位
Department of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL, USA.United States
通讯作者单位
Division of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.United States
文献类型
综述
期刊
Therapeutic advances in hematology2022
原文标识
PubMed 36505886 · DOI 10.1177/20406207221141511