Bendamustine in Combination With Rituximab for Previously Untreated Patients With Chronic Lymphocytic Leukemia: A Multicenter Phase II Trial of the German Chronic Lymphocytic Leukemia Study Group

Author:

Fischer Kirsten1,Cramer Paula1,Busch Raymonde1,Böttcher Sebastian1,Bahlo Jasmin1,Schubert Jöerg1,Pflüger Karl H.1,Schott Silke1,Goede Valentin1,Isfort Susanne1,von Tresckow Julia1,Fink Anna-Maria1,Bühler Andreas1,Winkler Dirk1,Kreuzer Karl-Anton1,Staib Peter1,Ritgen Matthias1,Kneba Michael1,Döhner Hartmut1,Eichhorst Barbara F.1,Hallek Michael1,Stilgenbauer Stephan1,Wendtner Clemens-Martin1

Affiliation:

1. Kirsten Fischer, Paula Cramer, Jasmin Bahlo, Silke Schott, Valentin Goede, Susanne Isfort, Julia von Tresckow, Anna-Maria Fink, Karl-Anton Kreuzer, Barbara F. Eichhorst, Michael Hallek, and Clemens-Martin Wendtner, University of Cologne, Cologne; Raymonde Busch, Institute of Medical Statistics and Epidemiology of the Technical University; Clemens-Martin Wendtner, Klinikum München-Schwabing, Munich; Sebastian Böttcher, Matthias Ritgen, and Michael Kneba, University Hospital, Kiel; Jörg Schubert,...

Abstract

Purpose We investigated the safety and efficacy of bendamustine and rituximab (BR) in previously untreated patients with chronic lymphocytic leukemia (CLL). Patients and Methods In all, 117 patients, age 34 to 78 years, 46.2% of patients at Binet stage C, and 25.6% of patients age 70 years or older received BR chemoimmunotherapy for first-line treatment of CLL. Bendamustine was administered at a dose of 90 mg/m2 on days 1 and 2 combined with 375 mg/m2 rituximab on day 0 of the first course and 500 mg/m2 on day 1 during subsequent courses for up to six courses. Results Overall response rate was 88.0% (95% CI, 80.7% to 100.0%) with a complete response rate of 23.1% and a partial response rate of 64.9%. Ninety percent of patients with del(11q), 94.7% with trisomy 12, 37.5% with del(17p), and 89.4% with unmutated IGHV status responded to treatment. After a median observation time of 27.0 months, median event-free survival was 33.9 months, and 90.5% of patients were alive. Grade 3 or 4 severe infections occurred in 7.7% of patients. Grade 3 or 4 adverse events for neutropenia, thrombocytopenia, and anemia were documented in 19.7%, 22.2%, and 19.7% of patients, respectively. Conclusion Chemoimmunotherapy with BR is effective and safe in patients with previously untreated CLL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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