We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.
Autologous stem cell transplantation was associated with better survival outcomes than rituximab-containing regimens in a cohort of patients with follicular lymphoma, according to results of a multicenter study.
Allogeneic transplantation, however, was not associated with improved survival.
The investigators aimed to determine whether autologous or allogeneic stem cell transplantation is optimal for patients with transformed follicular lymphoma, and whether either type of transplantation improved outcomes compared with rituximab (Rituxan, Genentech/Idec Pharmaceuticals)-containing chemotherapy alone.
OS served as the primary endpoint.
There were 97 patients in the autologous cohort, 22 patients in the allogeneic cohort and 53 who were treated with rituximab regimens.
After transformation, 5-year OS was 65% in the autologous group, 46% in the allogeneic group and 61% in the rituximab group (P=.24).
Five-year PFS rates were 55% for autologous stem cell transplantation, 46% for allogeneic transplant and 40% for rituximab (P=.12).
Multivariable analysis results indicated that autologous transplantation was associated with improvements in OS compared with rituximab (HR=0.13; 95% CI, 0.05-0.34). However, researchers did not observe similar improvement when they compared of allogeneic transplantation with rituximab (HR=0.44; 95% CI, 0.16-1.24).
Similar OS and PFS outcomes were observed in both stem cell transplantation groups.
The 5-year transplantation-related mortality rate was 5% in the autologous group and 23% in the allogeneic group.
We’re sorry, but an unexpected error has occurred.
Please refresh your browser and try again. If this error persists, please contact ITSupport@wyanokegroup.com for assistance.
Would you like to receive email reminders to complete your saved activities from Healio CME?
Activity saved! You'll receive reminders to complete your saved activities from Healio CME.