The MURANO study: final analysis and retreatment/crossover substudy results of VenR for patients with relapsed/refractory CLL
Abstract
Abstract Fixed-duration venetoclax-rituximab (VenR) in patients with relapsed/refractory chronic lymphocytic leukemia (CLL) in the phase 3 MURANO trial resulted in superior progression-free survival (PFS) and overall survival (OS) vs bendamustine-rituximab (BR). We report the final analyses of MURANO (median follow-up, 7 years). Patients were randomized to VenR (venetoclax 400 mg daily for 2 years plus monthly rituximab for 6 months; n = 194) or BR (6 months; n = 195). In a substudy, patients with progressive disease (PD) received VenR as retreatment or crossover from BR. At the final data cut (3 August 2022), the median PFS with VenR was 54.7 months vs 17.0 months with BR. The 7-year PFS with VenR was 23.0%. The 7-year OS was 69.6% and 51.0%, respectively. Among VenR-treated patients with undetectable minimal residual disease (MRD; uMRD) and no PD at end of treatment (EOT; n = 83), the median PFS from EOT was 52.5 vs 18.0 months in patients with MRD at EOT (n = 35; P < .0001). Fourteen patients had enduring uMRD. Three distinct mutations in BCL2 in 4 patients were identified. In the substudy, 25 patients were retreated with VenR, and 9 patients crossed over to VenR; the median PFS was 23 and 27 months, and the best overall response rate was 72% and 89%, respectively. At the end of combination treatment (EOCT), after retreatment or crossover, 8 and 6 patients achieved uMRD, respectively. No new safety findings were observed. Overall, these final MURANO analyses support consideration of fixed-duration VenR therapy for patients with relapsed/refractory CLL. This trial was registered at www.clinicaltrials.gov as #NCT02005471.
Article Details
Authors (22)
Arnon P. Kater
Amsterdam University Medical Center location University of Amsterdam, Department of Hematology
Rosemary Harrup
6Cancer and Blood Services, Royal Hobart Hospital and University of Tasmania, Hobart, TAS, Australia
Thomas J. Kipps
University of California, San Diego School of Medicine, La Jolla, California, United States
Barbara Eichhorst
Department I of Internal Medicine, Center of Integrated Oncology Aachen Bonn Cologne Düsseldorf, University Hospital of Cologne, Cologne, Germany
Carolyn J. Owen
5Division of Hematology and Hematological Malignancies, University of Calgary, Calgary, AB, Canada
Sarit Assouline
7Jewish General Hospital, Montreal, Canada
Nicole Lamanna
4Columbia University, New York, United States
Tadeusz Robak
36Department of Hematology, Medical University of Lodz, Lodz, Poland
Javier de la Serna
Hospital Universitario 12 de Octubre, Madrid
Ulrich Jaeger
Medical University of Vienna, Vienna, Austria
Guillaume Cartron
CHU Montpellier UMR5535, Montpellier, France
Marco Montillo
1ASST Grande Ospedale Metropolitano Niguarda, Department of Hematology and Oncology, Milano, Italy
Clemens Mellink
4AmsterdamUMC, Amsterdam, Netherlands
Anton W. Langerak
Brenda Chyla
Abbvie, North Chicago, Illinois, United States
Relja Popovic
Yanwen Jiang
12Genentech, Inc, South San Francisco, CA
Rosemary Millen
17Roche Products Ltd, Welwyn Garden City, United Kingdom
Marcus Lefebure
17BeOne Medicines Ltd, London, United Kingdom
Maria Thadani-Mulero
11Roche Products Ltd, Welwyn Garden City, United Kingdom
Michelle Boyer
12Genentech, Inc, South San Francisco, CA
John F. Seymour
Department of Haematology, Royal Melbourne Hospital and Peter MacCallum Cancer Centre, Melbourne, VIC, Australia