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:Combined or Sequential Treatment with Immune Checkpoint Inhibitors and Car-T Cell Therapies for the Management of Haematological Malignancies: A Systematic Review.
Combined or Sequential Treatment with Immune Checkpoint Inhibitors and Car-T Cell Therapies for the Management of Haematological Malignancies: A Systematic Review.
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。
本文旨在综述复发/难治性血液系统恶性肿瘤中,PD-1/PD-L1免疫检查点抑制剂(ICI)与CAR-T 细胞疗法联合或序贯使用的疗效和安全性证据。研究人员系统检索截至2022年11月21日的文献。纳入标准为:已报告结果的队列研究或临床试验,评估CAR-T 与PD-1/PD-L1抑制剂联合治疗复发/难治性血液肿瘤的疗效和/或安全性;单独评估ICI或CAR-T,或研究联合疗法治疗非血液系统实体瘤的文献被排除。研究采用专门清单进行质量评估,并提取疗效及安全性数据。共检索到1,867篇文章,最终纳入9篇早期研究;样本量较小,研究质量尚可。主要疾病为B细胞急性淋巴细胞白血病(B-ALL)和B细胞非霍奇金淋巴瘤(B-NHL),研究最多的联合方案是替沙仑赛联合帕博利珠单抗。疗效差异较大:该联合疗法在B-ALL中可能具有前景,但证据有限;在B-NHL中虽观察到令人鼓舞的应答,但总体未显示优于CAR-T 单药治疗。安全性特征总体上与CAR-T 单药治疗相当。
The aim of this paper was to review the available evidence on the efficacy and safety of combined or sequential use of PD-1/PD-L1 immune checkpoint inhibitors (ICI) and CAR-T cell therapies in relapsed/refractory (R/R) haematological malignancies. A systematic literature review was performed until 21 November 2022.
Inclusion criteria: cohort studies/clinical trials aimed at evaluating the efficacy and/or safety of the combination of CAR-T cell therapy with PD-1/PD-L1 inhibitors in R/R haematological malignancies, which had reported results. Those focusing only on ICI or CAR-T separately or evaluating the combination in other non-hematological solid tumours were excluded.
We used a specific checklist for quality assessment of the studies, and then we extracted data on efficacy or efficiency and safety. A total of 1867 articles were identified, and 9 articles were finally included (early phase studies, with small samples of patients and acceptable quality). The main pathologies were B-cell acute lymphoblastic leukaemia (B-ALL) and B-cell non-Hodgkin's lymphoma (B-NHL).
The most studied combination was tisagenlecleucel with pembrolizumab. In terms of efficacy, there is great variability: the combination could be a promising option in B-ALL, with modest data, and in B-NHL, although hopeful responses were received, the combination does not appear better than CAR-T cell monotherapy. The safety profile could be considered comparable to that described for CAR-T cell monotherapy.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。