Obinutuzumab plus Chlorambucil in Patients with CLL and Coexisting Conditions

Valentin Goede(University of Cologne), Kirsten Fischer(Integrated Oncology (United States)), Raymonde Busch, Anja Engelke(Integrated Oncology (United States)), Barbara Eichhorst(Integrated Oncology (United States)), Clemens‐Martin Wendtner(München Klinik Schwabing), Tatiana Chagorova, Javier de la Serna(Hospital Universitario 12 De Octubre), Marie‐Sarah Dilhuydy(Hôpital Cardiologique du Haut-Lévêque), Thomas Illmer, Stephen Opat(Monash Medical Centre), Carolyn Owen(University of Calgary), Olga Samoylova(Nizhny Novgorod Regional Clinical Hospital named after Semashko), Karl‐Anton Kreuzer(Integrated Oncology (United States)), Stephan Stilgenbauer(Universität Ulm), Hartmut Döhner(Universität Ulm), Anton W. Langerak(Erasmus MC), Matthias Ritgen(University Hospital Schleswig-Holstein), Michael Kneba(University Hospital Schleswig-Holstein), Elina Asikanius(Roche (Switzerland)), Kathryn Humphrey(Roche (United Kingdom)), Michael Wenger, Michael Hallek(University of Cologne)
New England Journal of Medicine
January 8, 2014
Cited by 1,498Open Access
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Abstract

BACKGROUND: The monoclonal anti-CD20 antibody rituximab, combined with chemotherapeutic agents, has been shown to prolong overall survival in physically fit patients with previously untreated chronic lymphocytic leukemia (CLL) but not in those with coexisting conditions. We investigated the benefit of the type 2, glycoengineered antibody obinutuzumab (also known as GA101) as compared with that of rituximab, each combined with chlorambucil, in patients with previously untreated CLL and coexisting conditions. METHODS: We randomly assigned 781 patients with previously untreated CLL and a score higher than 6 on the Cumulative Illness Rating Scale (CIRS) (range, 0 to 56, with higher scores indicating worse health status) or an estimated creatinine clearance of 30 to 69 ml per minute to receive chlorambucil, obinutuzumab plus chlorambucil, or rituximab plus chlorambucil. The primary end point was investigator-assessed progression-free survival. RESULTS: The patients had a median age of 73 years, creatinine clearance of 62 ml per minute, and CIRS score of 8 at baseline. Treatment with obinutuzumab-chlorambucil or rituximab-chlorambucil, as compared with chlorambucil monotherapy, increased response rates and prolonged progression-free survival (median progression-free survival, 26.7 months with obinutuzumab-chlorambucil vs. 11.1 months with chlorambucil alone; hazard ratio for progression or death, 0.18; 95% confidence interval [CI], 0.13 to 0.24; P<0.001; and 16.3 months with rituximab-chlorambucil vs. 11.1 months with chlorambucil alone; hazard ratio, 0.44; 95% CI, 0.34 to 0.57; P<0.001). Treatment with obinutuzumab-chlorambucil, as compared with chlorambucil alone, prolonged overall survival (hazard ratio for death, 0.41; 95% CI, 0.23 to 0.74; P=0.002). Treatment with obinutuzumab-chlorambucil, as compared with rituximab-chlorambucil, resulted in prolongation of progression-free survival (hazard ratio, 0.39; 95% CI, 0.31 to 0.49; P<0.001) and higher rates of complete response (20.7% vs. 7.0%) and molecular response. Infusion-related reactions and neutropenia were more common with obinutuzumab-chlorambucil than with rituximab-chlorambucil, but the risk of infection was not increased. CONCLUSIONS: Combining an anti-CD20 antibody with chemotherapy improved outcomes in patients with CLL and coexisting conditions. In this patient population, obinutuzumab was superior to rituximab when each was combined with chlorambucil. (Funded by F. Hoffmann-La Roche; ClinicalTrials.gov number, NCT01010061.).


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