Combined or Sequential Treatment with Immune Checkpoint Inhibitors and Car-T Cell Therapies for the Management of Haematological Malignancies: A Systematic Review

被引:2
|
作者
Perez-Moreno, Maria Antonia [1 ]
Ciudad-Gutierrez, Pablo [1 ]
Jaramillo-Ruiz, Didiana [1 ]
Reguera-Ortega, Juan Luis [2 ]
Abdel-kader Martin, Laila [1 ,3 ]
Flores-Moreno, Sandra [1 ]
机构
[1] Univ Hosp Virgen Rocio, Dept Pharm, Seville 41013, Spain
[2] Univ Seville, Univ Hosp Virgen Rocio, Dept Haematol, Inst Biomed Sevilla IBIS,CSIC, Seville 41012, Spain
[3] Univ Seville, Dept Pharm & Pharmaceut Technol, Seville 41012, Spain
关键词
checkpoint inhibitors; chimeric antigen receptor-T; combined therapy; haematologic tumour; systematic review; COMBINATION; BLOCKADE;
D O I
10.3390/ijms241914780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:15
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