Efficacy and Safety of Glofitamab Plus Polatuzumab Vedotin in Relapsed/Refractory Large B-Cell Lymphoma Including High-Grade B-Cell Lymphoma: Results From a Phase Ib/II Trial
Abstract
PURPOSE An unmet need remains for more effective therapies for relapsed/refractory (R/R) large B-cell lymphoma (LBCL), especially high-grade B-cell lymphoma (HGBCL). We present the primary analysis of a phase Ib/II study (ClinicalTrials.gov identifier: NCT03533283 ) investigating efficacy and safety of glofitamab plus polatuzumab vedotin (Glofit-Pola) in patients with R/R LBCL, including HGBCL and those who received previous chimeric antigen receptor (CAR) T-cell therapy. METHODS Patients received 1,000 mg obinutuzumab on Cycle (C)1 Day (D)1 (once daily). Polatuzumab vedotin (1.8 mg/kg) was given on C1D2 and D1 of C2–6 (21-day cycles; once daily). Glofitamab was given as step-up doses in C1 (D8, 2.5 mg; D15, 10 mg) followed by 30 mg on D1 of C2–12 (21-day cycles; once daily). Polatuzumab vedotin was given for six fixed-duration cycles, and glofitamab for 12. RESULTS As of September 2, 2024, 129 patients with LBCL (HGBCL; n = 44, 34.1%), received ≥1 dose of study treatment. The median age was 67 years (range, 23-84), and 63.6% were male. Patients had received a median of 2 (range, 1-7) previous lines of treatment (previous CAR T-cell therapy, n = 28, 21.7%). The independent review committee–assessed overall response rate was 78.3% (complete response rate, 59.7%). The median progression-free survival and overall survival (OS) were 12.3 and 33.8 months, respectively (median OS follow-up time, 32.7 months). The most common adverse event (AE) was cytokine release syndrome (43.4%; grade 1-2: 41.9%; one grade 5 event). Grade 3-4 AEs occurred in 58.9% of patients; 9.3% had grade 5 AEs, and 14.7% discontinued treatment because of AEs. CONCLUSION Glofit-Pola demonstrated high efficacy and durable responses, with manageable safety, in heavily pretreated patients with R/R LBCL, including patients with HGBCL and previous CAR T-cell therapy failure.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Martin Hutchings
15Department of Haematology, Rigshospitalet and University of Copenhagen, Copenhagen, Denmark
Anna Sureda
Institut Català d'Oncologia, Barcelona, Spain
Francesc Bosch
Department of Hematology, University Hospital Vall d’Hebron, Vall d’Hebron Institute of Oncology (VHIO), Barcelona
Thomas Stauffer Larsen
Odense University Hospital, Odense, Denmark
Paolo Corradini
8Istituto Nazionale Tumori IRCCS, Haematology, Milan, Italy
Abraham Avigdor
3Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel
Maria Jose Terol
7Hospital Clínico Universitario INCLIVA, University of Valencia, Valencia, Spain
Antonio Rueda Dominguez
8Virgen de la Victoria University Hospital, Málaga, Spain
Antonio Pinto
15Department of Hematology, Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico “Fondazione G Pascale”, Naples, Italy
Alan Skarbnik
19Novant Health Cancer Institute, Department of Hematology, Charlotte, United States
Raúl Córdoba
Judit Meszaros Jørgensen
Aarhus University Hospital, Aarhus, Denmark
Pier Luigi Zinzani
12IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia “Seràgnoli,” Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy
Wilfred Leung
15Genentech, Inc., South San Francisco, United States
Alessia Bottos
23F. Hoffmann-La Roche Ltd, Basel, Switzerland
Donghang Li
17Roche (China) Holding Ltd, Shanghai, China
James Relf
16Roche Products Ltd, Welwyn Garden City, United Kingdom
Maneesh Tandon
Roche Products Ltd, Welwyn Garden City, United Kingdom
Gila Sellam
19F. Hoffmann-La Roche Ltd, Basel, Switzerland
Giuseppe Gritti
20ASST Ospedale Papa Giovanni XXIII, Bergamo, Italy