Mosunetuzumab With Response-Adapted Polatuzumab Vedotin and Obinutuzumab in Untreated Indolent B-Cell Non-Hodgkin Lymphoma
Abstract
PURPOSE Chemoimmunotherapy has been the standard approach for untreated indolent B-cell lymphoma. We hypothesized that initial use of the CD3/CD20 bispecific mosunetuzumab followed by response-adapted polatuzumab vedotin and obinutuzumab would yield an optimized chemotherapy-free approach. METHODS Previously untreated patients with follicular lymphoma (FL) and marginal zone lymphoma (MZL) with indication for treatment received eight cycles of mosunetuzumab. Those not achieving a complete response (CR) by positron emission tomography-computed tomography (PET-CT) following mosunetuzumab could go on to receive six cycles of polatuzumab vedotin and obinutuzumab. The primary end point was best overall response rate (ORR) of CR by fluorodeoxyglucose-PET-CT. RESULTS The 42 enrolled patients had a median age of 60 years (range, 36-83), 39 were stage III to IV (93%), 37 (88%) had FL, and 13 (31%) had bulk >7 cm. The end-of-treatment ORR and CR rates were 100% and 86%, respectively. The ORR and CR to mosunetuzumab alone were 100% and 71%, respectively. With a median follow-up of 34 months, the 2-year progression-free survival (PFS) was 89% (95% CI, 80 to 100) and the 2-year overall survival was 100%. The four progression events included CD20 loss (2) and histologic transformation (2). Cytokine release syndrome occurred in 27 patients (64%), but all were grade 1. No patients required tocilizumab. CONCLUSION Single-agent mosunetuzumab as well as response-adapted polatuzumab vedotin and obinutuzumab yield encouraging CR rates and PFS with limited toxicity among previously untreated patients with FL and MZL. This chemotherapy-free strategy may provide a template for larger study designs for personalized approaches in this population that balances efficacy with safety.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (17)
Ryan C. Lynch
Christina Poh
2City of Hope, Duarte, United States
Mazyar Shadman
Brian G. Till
Mengyang Di
5Fred Hutchinson Cancer Research Center, Seattle, United States
Chaitra S. Ujjani
7Seattle Cancer Care Alliance, Fred Hutchinson Cancer Center, Seattle, WA
Vikram Raghunathan
1Fred Hutchinson Cancer Center, Seattle, United States
Stephen D. Smith
19Division of Hematology and Oncology, Fred Hutchinson Cancer Center, Seattle, WA
David Maloney
1Fred Hutchinson Cancer Center, Seattle, United States
Daria Gausman
1Fred Hutchinson Cancer Center, Seattle, United States
Heather Rasmussen
1Fred Hutchinson Cancer Center, Seattle, United States
David A. Russler-Germain
Washington University School of Medicine, Saint Louis, MO
Todd A. Fehniger
David M. Kurtz
Ash Alizadeh
4Stanford University, Stanford, United States
Jenna Voutsinas
1Fred Hutchinson Cancer Center, Seattle, United States
Ajay K. Gopal
Fred Hutchinson Cancer Center and University of Washington