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Outcomes with chimeric antigen receptor t-cell therapy in relapsed or refractory acute myeloid leukemia: a systematic review and meta-analysis

BACKGROUND: We conducted a systematic review and meta-analysis to evaluate outcomes following chimeric antigen receptor T cell (CAR-T) therapy in relapsed/refractory acute myeloid leukemia (RR-AML). METHODS: We performed a literature search on PubMed, Cochrane Library, and Clinicaltrials.gov. After...

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Detalles Bibliográficos
Autores principales: Shahzad, Moazzam, Nguyen, Andrea, Hussain, Ali, Ammad-Ud-Din, Mohammad, Faisal, Muhammad Salman, Tariq, Ezza, Ali, Fatima, Butt, Atif, Anwar, Iqra, Chaudhary, Sibgha Gull, Lutfi, Forat, Ahmed, Nausheen, Singh, Anurag K., Hematti, Peiman, McGuirk, Joseph P., Mushtaq, Muhammad Umair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164930/
https://www.ncbi.nlm.nih.gov/pubmed/37168849
http://dx.doi.org/10.3389/fimmu.2023.1152457
Descripción
Sumario:BACKGROUND: We conducted a systematic review and meta-analysis to evaluate outcomes following chimeric antigen receptor T cell (CAR-T) therapy in relapsed/refractory acute myeloid leukemia (RR-AML). METHODS: We performed a literature search on PubMed, Cochrane Library, and Clinicaltrials.gov. After screening 677 manuscripts, 13 studies were included. Data was extracted following PRISMA guidelines. Pooled analysis was done using the meta-package by Schwarzer et al. Proportions with 95% confidence intervals (CI) were computed. RESULTS: We analyzed 57 patients from 10 clinical trials and 3 case reports. The pooled complete and overall response rates were 49.5% (95% CI 0.18-0.81, I(2 )=65%) and 65.2% (95% CI 0.36-0.91, I(2 )=57%). The pooled incidence of cytokine release syndrome, immune-effector cell associated neurotoxicity syndrome, and graft-versus-host disease was estimated as 54.4% (95% CI 0.17-0.90, I(2 )=77%), 3.9% (95% CI 0.00-0.19, I(2 )=22%), and 1.6% (95%CI 0.00-0.21, I(2 )=33%), respectively. CONCLUSION: CAR-T therapy has demonstrated modest efficacy in RR-AML. Major challenges include heterogeneous disease biology, lack of a unique targetable antigen, and immune exhaustion.