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嵌合抗原受体T细胞(CAR-T)疗法在弥漫性大B细胞淋巴瘤二线治疗中的作用。

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

作者信息

Albanyan Omar, Chavez Julio, Munoz Javier

机构信息

Department of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL, USA.

Adult Hematology-Oncology and SCT, King Fahad Specialist Hospital, Dammam 32253, Saudi Arabia.

出版信息

Ther Adv Hematol. 2022 Dec 6;13:20406207221141511. doi: 10.1177/20406207221141511. eCollection 2022.

DOI:10.1177/20406207221141511
PMID:36505886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9730015/
Abstract

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.

摘要

在大约三十年的时间里,自体造血细胞移植(auto-HCT)一直是一线治疗后复发/难治性(R/R)弥漫性大B细胞淋巴瘤(DLBCL)患者的标准治疗方法。由于化疗强度以及自体造血细胞移植后复发患者的比例,这种方法存在局限性。自从抗CD19嵌合抗原受体T细胞(CAR-T)疗法和新型药物获批以来,DLBCL的治疗模式发生了显著变化。抗CD19 CAR-T疗法首次获批用于经过两种或更多线先前治疗后复发的DLBCL,具有持久反应,超过50%的患者在5年随访时仍然存活。在此,我们讨论了在二线治疗环境中使用阿基仑赛、替雷利珠单抗和利舒卡提单抗进行的近期随机3期临床试验,与在完成化疗免疫治疗后12个月内患有R/R DLBCL的适合移植患者的标准治疗方法相比,这可能会改变DLBCL的治疗算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/22d1478e5ff4/10.1177_20406207221141511-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/380bfffbb450/10.1177_20406207221141511-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/f145ab480ee2/10.1177_20406207221141511-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/22d1478e5ff4/10.1177_20406207221141511-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/380bfffbb450/10.1177_20406207221141511-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/f145ab480ee2/10.1177_20406207221141511-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ad/9730015/22d1478e5ff4/10.1177_20406207221141511-fig3.jpg

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