Bibliographic Details
Title: |
A systematic review and meta-analysis on utilizing anti-CD19 chimeric antigen receptor T-cell therapy as a second-line treatment for relapsed and refractory diffuse large B-cell lymphoma. |
Authors: |
Asghar, Kanwal, Zafar, Maryam, Holland, Eva, Bin Abduljabbar, Ali, Albagoush, Sara A., Asghar, Noureen, Sood, Akshat, Dufani, Jalal M., Thirumalaredy, Joseph, DeVrieze, Bradley, Tauseef, Abubakar, Husnain, Muhammad |
Source: |
Frontiers in Oncology; 2024, p1-10, 10p |
Subject Terms: |
DIFFUSE large B-cell lymphomas, B cell lymphoma, CLINICAL trials, CHIMERIC antigen receptors, CELLULAR therapy |
Abstract: |
Introduction: Inconsistent results observed in recent phase III trials assessing chimeric antigenic receptor T (CAR-T) cell therapy as a second-line treatment compared to standard of care (SOC) in patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) prompted a meta-analysis to assess the effectiveness of CAR-T cell therapy in this setting. Methods: Random-effects meta-analysis was conducted to pool effect estimates for comparison between CAR-T cell therapy and SOC. Mixed treatment comparisons were made using a frequentist network meta-analysis approach. Results: Meta-analysis of three trials with 865 patients showed significant improvement in event-free survival (EFS: HR: 0.51; 95% CI: 0.27-0.97; I2: 92%), progression-free survival (PFS: HR: 0.47; 95% CI: 0.37-0.60; I2: 0%) with CAR-T cell therapy compared to SOC. Although there was a signal of potential overall survival (OS) improvement with CAR-T cell therapy, the difference was not statistically significant between the two groups (HR 0.76; 95% CI: 0.56 to 1.03; I2: 29%). Mixed treatment comparisons showed significant EFS benefitwith liso-cel (HR: 0.37; 95%CI: 0.22-0.61) and axi-cel (HR: 0.42; 95% CI: 0.29-0.61) compared to tisa-cel. Discussion: CAR-T cell therapy, as a second-line treatment, appears to be effective in achieving higher response rates and delaying the disease progression compared to SOC in R/R DLBCL. [ABSTRACT FROM AUTHOR] |
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Database: |
Complementary Index |