Venetoclax and Obinutuzumab in Patients with CLL and Coexisting Conditions

Kirsten Fischer(University of Cologne), Othman Al‐Sawaf(University of Cologne), Jasmin Bahlo(University of Cologne), Anna‐Maria Fink(University of Cologne), Maneesh Tandon(Düsseldorf University Hospital), Mark Dixon(Düsseldorf University Hospital), Sandra Robrecht(University of Cologne), Simon Warburton(Düsseldorf University Hospital), Kathryn Humphrey(Düsseldorf University Hospital), Olga Samoylova(Düsseldorf University Hospital), A. M. Liberati(University of Perugia), Javier Pinilla‐Ibarz(Moffitt Cancer Center), Stephen Opat(Düsseldorf University Hospital), Liliya Sivcheva(Düsseldorf University Hospital), Katell Le Dû(Düsseldorf University Hospital), Laura Fogliatto(Düsseldorf University Hospital), Carsten Utoft Niemann(Copenhagen University Hospital), Robert Weinkove(Malaghan Institute of Medical Research), Sue Robinson(Queen Elizabeth II Health Sciences Centre), Thomas J. Kipps(University of California San Diego), Sebastian Böettcher(Düsseldorf University Hospital), Eugen Tausch(Universität Ulm), Rod Humerickhouse(AbbVie (United States)), Barbara Eichhorst(University of Cologne), Clemens‐Martin Wendtner(Düsseldorf University Hospital), Anton W. Langerak(Erasmus MC), Karl-Anton Kreuzer(University of Cologne), Matthias Ritgen(Christian-Albrechts-Universität zu Kiel), Valentin Goede(Düsseldorf University Hospital), Stephan Stilgenbauer(Universität Ulm), Mehrdad Mobasher(Düsseldorf University Hospital), Michael Hallek(University of Cologne)
New England Journal of Medicine
June 4, 2019
Cited by 843

Abstract

BACKGROUND: The BCL2 inhibitor venetoclax has shown activity in patients with chronic lymphocytic leukemia (CLL), but its efficacy in combination with other agents in patients with CLL and coexisting conditions is not known. METHODS: In this open-label, phase 3 trial, we investigated fixed-duration treatment with venetoclax and obinutuzumab in patients with previously untreated CLL and coexisting conditions. Patients with a score of greater than 6 on the Cumulative Illness Rating Scale (scores range from 0 to 56, with higher scores indicating more impaired function of organ systems) or a calculated creatinine clearance of less than 70 ml per minute were randomly assigned to receive venetoclax-obinutuzumab or chlorambucil-obinutuzumab. The primary end point was investigator-assessed progression-free survival. The safety of each regimen was also evaluated. RESULTS: deletion, mutation, or both and in patients with unmutated immunoglobulin heavy-chain genes. Grade 3 or 4 neutropenia occurred in 52.8% of patients in the venetoclax-obinutuzumab group and in 48.1% of patients in the chlorambucil-obinutuzumab group, and grade 3 or 4 infections occurred in 17.5% and 15.0%, respectively. All-cause mortality was 9.3% in the venetoclax-obinutuzumab group and 7.9% in the chlorambucil-obinutuzumab group. These differences were not significant. CONCLUSIONS: Among patients with untreated CLL and coexisting conditions, venetoclax-obinutuzumab was associated with longer progression-free survival than chlorambucil-obinutuzumab. (Funded by F. Hoffmann-La Roche and AbbVie; ClinicalTrials.gov number, NCT02242942.).


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