Background: In an analysis of the primary outcome of this phase 3 trial, patients with early relapsed or refractory large B-cell lymphoma who received axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor T-cell therapy, as second-line treatment had significantly longer event-free survival than those who received standard care. Data were needed on longer-term outcomes. Methods: In this trial, we randomly assigned patients with early relapsed or refractory large B-cell lymphoma in a 1:1 ratio to receive either axi-cel or standard care (two to three cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem-cell transplantation in patients who had a response). The primary outcome was event-free survival, and key secondary outcomes were response and overall survival. Here, we report the results of the prespecified overall survival analysis at 5 years after the first patient underwent randomization. Results: A total of 359 patients underwent randomization to receive axi-cel (180 patients) or standard care (179 patients). At a median follow-up of 47.2 months, death had been reported in 82 patients in the axi-cel group and in 95 patients in the standard-care group. The median overall survival was not reached in the axi-cel group and was 31.1 months in the standard-care group; the estimated 4-year overall survival was 54.6% and 46.0%, respectively (hazard ratio for death, 0.73; 95% confidence interval [CI], 0.54 to 0.98; P = 0.03 by stratified two-sided log-rank test). This increased survival with axi-cel was observed in the intention-to-treat population, which included 74% of patients with primary refractory disease and other high-risk features. The median investigator-assessed progression-free survival was 14.7 months in the axi-cel group and 3.7 months in the standard-care group, with estimated 4-year percentages of 41.8% and 24.4%, respectively (hazard ratio, 0.51; 95% CI, 0.38 to 0.67). No new treatment-related deaths had occurred since the primary analysis of event-free survival. Conclusions: At a median follow-up of 47.2 months, axi-cel as second-line treatment for patients with early relapsed or refractory large B-cell lymphoma resulted in significantly longer overall survival than standard care. (Funded by Kite; ZUMA-7 ClinicalTrials.gov number, NCT03391466.).

Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma / Westin, Jason R.; Oluwole, Olalekan O.; Kersten, Marie José; Miklos, David B.; Perales, Miguel-Angel; Ghobadi, Armin; Rapoport, Aaron P.; Sureda, Anna; Jacobson, Caron A.; Farooq, Umar; van Meerten, Tom; Ulrickson, Matthew; Elsawy, Mahmoud; Leslie, Lori A.; Chaganti, Sridhar; Dickinson, Michael; Dorritie, Kathleen; Reagan, Patrick M.; McGuirk, Joseph; Song, Kevin W.; Riedell, Peter A.; Minnema, Monique C.; Yang, Yin; Vardhanabhuti, Saran; Filosto, Simone; Cheng, Paul; Shahani, Shilpa A.; Schupp, Marco; To, Christina; Locke, Frederick L.; Zinzani P.. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - ELETTRONICO. - 389:2(2023), pp. 148-157. [10.1056/nejmoa2301665]

Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma

Zinzani P.
2023

Abstract

Background: In an analysis of the primary outcome of this phase 3 trial, patients with early relapsed or refractory large B-cell lymphoma who received axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor T-cell therapy, as second-line treatment had significantly longer event-free survival than those who received standard care. Data were needed on longer-term outcomes. Methods: In this trial, we randomly assigned patients with early relapsed or refractory large B-cell lymphoma in a 1:1 ratio to receive either axi-cel or standard care (two to three cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem-cell transplantation in patients who had a response). The primary outcome was event-free survival, and key secondary outcomes were response and overall survival. Here, we report the results of the prespecified overall survival analysis at 5 years after the first patient underwent randomization. Results: A total of 359 patients underwent randomization to receive axi-cel (180 patients) or standard care (179 patients). At a median follow-up of 47.2 months, death had been reported in 82 patients in the axi-cel group and in 95 patients in the standard-care group. The median overall survival was not reached in the axi-cel group and was 31.1 months in the standard-care group; the estimated 4-year overall survival was 54.6% and 46.0%, respectively (hazard ratio for death, 0.73; 95% confidence interval [CI], 0.54 to 0.98; P = 0.03 by stratified two-sided log-rank test). This increased survival with axi-cel was observed in the intention-to-treat population, which included 74% of patients with primary refractory disease and other high-risk features. The median investigator-assessed progression-free survival was 14.7 months in the axi-cel group and 3.7 months in the standard-care group, with estimated 4-year percentages of 41.8% and 24.4%, respectively (hazard ratio, 0.51; 95% CI, 0.38 to 0.67). No new treatment-related deaths had occurred since the primary analysis of event-free survival. Conclusions: At a median follow-up of 47.2 months, axi-cel as second-line treatment for patients with early relapsed or refractory large B-cell lymphoma resulted in significantly longer overall survival than standard care. (Funded by Kite; ZUMA-7 ClinicalTrials.gov number, NCT03391466.).
2023
Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma / Westin, Jason R.; Oluwole, Olalekan O.; Kersten, Marie José; Miklos, David B.; Perales, Miguel-Angel; Ghobadi, Armin; Rapoport, Aaron P.; Sureda, Anna; Jacobson, Caron A.; Farooq, Umar; van Meerten, Tom; Ulrickson, Matthew; Elsawy, Mahmoud; Leslie, Lori A.; Chaganti, Sridhar; Dickinson, Michael; Dorritie, Kathleen; Reagan, Patrick M.; McGuirk, Joseph; Song, Kevin W.; Riedell, Peter A.; Minnema, Monique C.; Yang, Yin; Vardhanabhuti, Saran; Filosto, Simone; Cheng, Paul; Shahani, Shilpa A.; Schupp, Marco; To, Christina; Locke, Frederick L.; Zinzani P.. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - ELETTRONICO. - 389:2(2023), pp. 148-157. [10.1056/nejmoa2301665]
Westin, Jason R.; Oluwole, Olalekan O.; Kersten, Marie José; Miklos, David B.; Perales, Miguel-Angel; Ghobadi, Armin; Rapoport, Aaron P.; Sureda, Anna; Jacobson, Caron A.; Farooq, Umar; van Meerten, Tom; Ulrickson, Matthew; Elsawy, Mahmoud; Leslie, Lori A.; Chaganti, Sridhar; Dickinson, Michael; Dorritie, Kathleen; Reagan, Patrick M.; McGuirk, Joseph; Song, Kevin W.; Riedell, Peter A.; Minnema, Monique C.; Yang, Yin; Vardhanabhuti, Saran; Filosto, Simone; Cheng, Paul; Shahani, Shilpa A.; Schupp, Marco; To, Christina; Locke, Frederick L.; Zinzani P.
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