Axi-cel vs. tisa-cel vs. liso-cel in R/R DLBCL: Meta-analysis of the efficacy-safety trade-off.

E Ebtisam Hamed (Elrazi University, Khartoum, Sudan) M Mulham Ombada (Khartoum University, Khartoum, No, Sudan) I Iman Osman (University of Medical Sciences and Technology, Khartoum, Sudan) E Elaf Sabri Khalil Mergani (University of Al-Neelaine, Khartoum, Sudan) M Moayad Mudawi (Elrazi University, Khartoum, Sudan) R Roaa Suliman (University of Gezira, Madani, Sudan) N Nadir Abdelrahman (University of Gezira, Michigan) M Matthew Joseph Cortese (Roswell Park Comprehensive Cancer Center, Buffalo, NY)

Abstract

e22002 Background: CD19-directed chimeric antigen receptor T-cell (CAR-T) therapies have improved outcomes for patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Direct comparisons between approved products—axicabtagene ciloleucel (axi-cel), tisagenlecleucel (tisa-cel), and lisocabtagene maraleucel (liso-cel)—remain limited, complicating evidence-based selection in clinical practice. Methods: We performed a PRISMA-compliant systematic review and meta-analysis of randomized clinical trials and real-world studies (through March 2025) evaluating long-term efficacy and safety of commercially available CD19 CAR-T therapies in adults with R/R DLBCL. PubMed, Embase, Cochrane Library, and conference abstracts were searched. Pooled estimates were calculated using random-effects models. Results: Twenty-five studies (4,067 patients; median follow-up 24.6 months) were included. The pooled overall response rate (ORR) was 74% (95% CI, 69–79%), with a complete response (CR) rate of 52% (95% CI, 43–60%). Axi-cel showed the highest ORR (77%; 95% CI, 72–81%) and CR rate (47%; 95% CI, 45–50%). Pooled 1-year progression-free survival (PFS) was 43% (95% CI, 37–49%), and 1-year overall survival (OS) was 66% (95% CI, 59–73%). Safety profiles differed significantly: axi-cel was associated with the highest incidence of immune effector cell-associated neurotoxicity syndrome (ICANS; 34%), while liso-cel had the lowest (9%; 95% CI, 6–13%). Rates of cytokine release syndrome were comparable across products. Conclusions: All approved CD19 CAR-T therapies provide meaningful clinical benefit in R/R DLBCL, but with distinct efficacy–toxicity profiles. These findings support a personalized approach to product selection, integrating patient comorbidities, disease aggressiveness, and institutional experience. Pooled efficacy outcomes of CD19 CAR-T therapies. Outcome Axi-cel (95% CI) Tisa-cel (95% CI) Liso-cel (95% CI) Overall Pooled (95% CI) Overall response rate (ORR), % 77% [72–81] 54% [45–64] 74% [68–79] 74% [69–79] Complete response (CR), % 47% [45–50] 42% [38–46] 49% [46–51] 52% [43–60] 1-year PFS, % 45% [42–47] 28% [25–32] 26% [23–28] 43% [37–49] 1-year OS, % 65%[63–68] 56%[51–60] 55%[52–58] 66%[59–73] CI, confidence interval; ORR, overall response rate; CR, complete response; PFS, progression-free survival; OS, overall survival. Interpretation: The overall pooled estimates (right column) represent a weighted average across all included studies and patient populations. The superior ORR/CR with axi-cel and the favorable safety profile of liso-cel (see main text) underscore the need for treatment personalization.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (8)

E

Ebtisam Hamed

Elrazi University, Khartoum, Sudan

M

Mulham Ombada

Khartoum University, Khartoum, No, Sudan

I

Iman Osman

University of Medical Sciences and Technology, Khartoum, Sudan

E

Elaf Sabri Khalil Mergani

University of Al-Neelaine, Khartoum, Sudan

M

Moayad Mudawi

Elrazi University, Khartoum, Sudan

R

Roaa Suliman

University of Gezira, Madani, Sudan

N

Nadir Abdelrahman

University of Gezira, Michigan

M

Matthew Joseph Cortese

Roswell Park Comprehensive Cancer Center, Buffalo, NY