Late relapse after CAR-T cell therapy for adult patients with hematologic malignancies: A definite evidence from systematic review and meta-analysis on individual data

• Published in: Pharmacological research 2023-04, Vol.190, p.106742-106742, Article 106742
• Main Authors: Zinzi, Alessia, Gaio, Mario, Liguori, Valerio, Cagnotta, Cecilia, Paolino, Donatella, Paolisso, Giuseppe, Castaldo, Giuseppe, Nicoletti, Giovanni Francesco, Rossi, Francesco, Capuano, Annalisa, Rafaniello, Concetta
• Format: Article
• Language: English
• Subjects: Adult; Cell- and Tissue-Based Therapy; Chimeric antigen receptor; Chronic Disease; Duration of response; Hematologic malignancies; Hematologic Neoplasms - therapy; Humans; Meta-analysis; Multiple Myeloma; Receptors, Chimeric Antigen; Recurrence; Relapse; Systematic review; T-Lymphocytes
• ISSN: 1043-6618; 1096-1186
• DOI: 10.1016/j.phrs.2023.106742

Chimeric Antigen Receptor (CAR)-modified T lymphocytes represent one of the most innovative and promising approaches to treating hematologic malignancies. CAR-T cell therapy is currently being used for the treatment of relapsed/refractory (r/r) B-cell malignancies including Acute Lymphoblastic Leukemia, Large B-Cell Lymphoma, Follicular Lymphoma, Multiple Myeloma and Mantle Cell Lymphoma. Despite the unprecedented clinical success, one of the major issues of the approved CAR-T cell therapy – tisagenlecleucel, axicabtagene, lisocabtagene, idecabtagene, ciltacabtagene and brexucabtagene – is the uncertainty about its persistence which in turn could lead to weak or no response to therapy with malignancy recurrence. Here we show that the prognosis of patients who do not respond to CAR-T cell therapy is still an unmet medical need. We performed a systematic review and meta-analysis collecting individual data on Duration of Response from at least 12-month follow-up studies. We found that the pooled prevalence of relapse within the first 12 months after CAR-T infusion was 61% (95% CI, 43%−78%); moreover, one year after the infusion, the analysis highlighted a pooled prevalence of relapse of 24% (95% CI, 11%−42%). Our results suggest that identifying potential predictive biomarkers of response to CAR-T therapy, especially for patients affected by the advanced stage of blood malignancies, could lead to stratification of the eligible population to that therapy, recognizing which patients will benefit and which will not, helping regulators to make decision in that way. [Display omitted]