Point of Care Landmark-class

Five-Year ZUMA-1 Follow-Up: 43% of Refractory Lymphoma Patients Alive After Axi-cel CAR T Therapy

The 5-year follow-up of the ZUMA-1 registrational trial of axicabtagene ciloleucel in 101 patients with refractory large B-cell lymphoma showed a 42.6% estimated 5-year overall survival rate, with 31% of patients maintaining ongoing responses. No new safety signals emerged with extended follow-up, and polyclonal B-cell recovery occurred in 91% of evaluable patients by three years. These landmark data support the curative potential of CAR T-cell therapy in a subset of patients with aggressive lymphoma previously considered incurable.

The original study

Five-year follow-up of ZUMA-1 supports the curative potential of axicabtagene ciloleucel in refractory large B-cell lymphoma.

Authors
Neelapu SS, Jacobson CA, Ghobadi A, Miklos DB, Lekakis LJ, Oluwole OO, et al.
Journal
Blood
Type
Multicenter Study, Journal Article, Research Support, Non-U.S. Gov't
PMID
36821768
Read the original study →

Original abstract

In phase 2 of ZUMA-1, a single-arm, multicenter, registrational trial, axicabtagene ciloleucel (axi-cel) autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy demonstrated durable responses at 2 years in patients with refractory large B-cell lymphoma (LBCL). Here, we assessed outcomes in ZUMA-1 after 5 years of follow-up. Eligible adults received lymphodepleting chemotherapy followed by axi-cel (2 × 106 cells per kg). Investigator-assessed response, survival, safety, and pharmacokinetics were assessed in patients who had received treatment. The objective response rate in these 101 patients was 83% (58% complete response rate); with a median follow-up of 63.1 months, responses were ongoing in 31% of patients at data cutoff. Median overall survival (OS) was 25.8 months, and the estimated 5-year OS rate was 42.6%. Disease-specific survival (excluding deaths unrelated to disease progression) estimated at 5 years was 51.0%. No new serious adverse events or deaths related to axi-cel were observed after additional follow-up. Peripheral blood B cells were detectable in all evaluable patients at 3 years with polyclonal B-cell recovery in 91% of patients. Ongoing responses at 60 months were associated with early CAR T-cell expansion. In conclusion, this 5-year follow-up analysis of ZUMA-1 demonstrates sustained overall and disease-specific survival, with no new safety signals in patients with refractory LBCL. Protracted B-cell aplasia was not required for durable responses. These findings support the curative potential of axi-cel in a subset of patients with aggressive B-cell lymphomas. This trial was registered at ClinicalTrials.gov, as #NCT02348216.