Mosunetuzumab With Response-Adapted Polatuzumab Vedotin and Obinutuzumab in Untreated Indolent B-Cell Non-Hodgkin Lymphoma

R Ryan C. Lynch C Christina Poh (2City of Hope, Duarte, United States) M Mazyar Shadman B Brian G. Till M Mengyang Di (5Fred Hutchinson Cancer Research Center, Seattle, United States) C Chaitra S. Ujjani (7Seattle Cancer Care Alliance, Fred Hutchinson Cancer Center, Seattle, WA) V Vikram Raghunathan (1Fred Hutchinson Cancer Center, Seattle, United States) S Stephen D. Smith (19Division of Hematology and Oncology, Fred Hutchinson Cancer Center, Seattle, WA) D David Maloney (1Fred Hutchinson Cancer Center, Seattle, United States) D Daria Gausman (1Fred Hutchinson Cancer Center, Seattle, United States) H Heather Rasmussen (1Fred Hutchinson Cancer Center, Seattle, United States) D David A. Russler-Germain (Washington University School of Medicine, Saint Louis, MO) T Todd A. Fehniger D David M. Kurtz A Ash Alizadeh (4Stanford University, Stanford, United States) J Jenna Voutsinas (1Fred Hutchinson Cancer Center, Seattle, United States) A Ajay K. Gopal (Fred Hutchinson Cancer Center and University of Washington)

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

Volume / Issue Vol. 1, Issue 1
Published August 14, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

R

Ryan C. Lynch

C

Christina Poh

2City of Hope, Duarte, United States

M

Mazyar Shadman

B

Brian G. Till

M

Mengyang Di

5Fred Hutchinson Cancer Research Center, Seattle, United States

C

Chaitra S. Ujjani

7Seattle Cancer Care Alliance, Fred Hutchinson Cancer Center, Seattle, WA

V

Vikram Raghunathan

1Fred Hutchinson Cancer Center, Seattle, United States

S

Stephen D. Smith

19Division of Hematology and Oncology, Fred Hutchinson Cancer Center, Seattle, WA

D

David Maloney

1Fred Hutchinson Cancer Center, Seattle, United States

D

Daria Gausman

1Fred Hutchinson Cancer Center, Seattle, United States

H

Heather Rasmussen

1Fred Hutchinson Cancer Center, Seattle, United States

D

David A. Russler-Germain

Washington University School of Medicine, Saint Louis, MO

T

Todd A. Fehniger

D

David M. Kurtz

A

Ash Alizadeh

4Stanford University, Stanford, United States

J

Jenna Voutsinas

1Fred Hutchinson Cancer Center, Seattle, United States

A

Ajay K. Gopal

Fred Hutchinson Cancer Center and University of Washington