The MURANO study: final analysis and retreatment/crossover substudy results of VenR for patients with relapsed/refractory CLL

A Arnon P. Kater (Amsterdam University Medical Center location University of Amsterdam, Department of Hematology) R Rosemary Harrup (6Cancer and Blood Services, Royal Hobart Hospital and University of Tasmania, Hobart, TAS, Australia) T Thomas J. Kipps (University of California, San Diego School of Medicine, La Jolla, California, United States) B Barbara Eichhorst (Department I of Internal Medicine, Center of Integrated Oncology Aachen Bonn Cologne Düsseldorf, University Hospital of Cologne, Cologne, Germany) C Carolyn J. Owen (5Division of Hematology and Hematological Malignancies, University of Calgary, Calgary, AB, Canada) S Sarit Assouline (7Jewish General Hospital, Montreal, Canada) N Nicole Lamanna (4Columbia University, New York, United States) T Tadeusz Robak (36Department of Hematology, Medical University of Lodz, Lodz, Poland) J Javier de la Serna (Hospital Universitario 12 de Octubre, Madrid) U Ulrich Jaeger (Medical University of Vienna, Vienna, Austria) G Guillaume Cartron (CHU Montpellier UMR5535, Montpellier, France) M Marco Montillo (1ASST Grande Ospedale Metropolitano Niguarda, Department of Hematology and Oncology, Milano, Italy) C Clemens Mellink (4AmsterdamUMC, Amsterdam, Netherlands) A Anton W. Langerak B Brenda Chyla (Abbvie, North Chicago, Illinois, United States) R Relja Popovic Y Yanwen Jiang (12Genentech, Inc, South San Francisco, CA) R Rosemary Millen (17Roche Products Ltd, Welwyn Garden City, United Kingdom) M Marcus Lefebure (17BeOne Medicines Ltd, London, United Kingdom) M Maria Thadani-Mulero (11Roche Products Ltd, Welwyn Garden City, United Kingdom) M Michelle Boyer (12Genentech, Inc, South San Francisco, CA) J John F. Seymour (Department of Haematology, Royal Melbourne Hospital and Peter MacCallum Cancer Centre, Melbourne, VIC, Australia)

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

Journal Blood
Volume / Issue Vol. 145, Issue 23
Published June 05, 2025
Pages 2733-2745
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (22)

A

Arnon P. Kater

Amsterdam University Medical Center location University of Amsterdam, Department of Hematology

R

Rosemary Harrup

6Cancer and Blood Services, Royal Hobart Hospital and University of Tasmania, Hobart, TAS, Australia

T

Thomas J. Kipps

University of California, San Diego School of Medicine, La Jolla, California, United States

B

Barbara Eichhorst

Department I of Internal Medicine, Center of Integrated Oncology Aachen Bonn Cologne Düsseldorf, University Hospital of Cologne, Cologne, Germany

C

Carolyn J. Owen

5Division of Hematology and Hematological Malignancies, University of Calgary, Calgary, AB, Canada

S

Sarit Assouline

7Jewish General Hospital, Montreal, Canada

N

Nicole Lamanna

4Columbia University, New York, United States

T

Tadeusz Robak

36Department of Hematology, Medical University of Lodz, Lodz, Poland

J

Javier de la Serna

Hospital Universitario 12 de Octubre, Madrid

U

Ulrich Jaeger

Medical University of Vienna, Vienna, Austria

G

Guillaume Cartron

CHU Montpellier UMR5535, Montpellier, France

M

Marco Montillo

1ASST Grande Ospedale Metropolitano Niguarda, Department of Hematology and Oncology, Milano, Italy

C

Clemens Mellink

4AmsterdamUMC, Amsterdam, Netherlands

A

Anton W. Langerak

B

Brenda Chyla

Abbvie, North Chicago, Illinois, United States

R

Relja Popovic

Y

Yanwen Jiang

12Genentech, Inc, South San Francisco, CA

R

Rosemary Millen

17Roche Products Ltd, Welwyn Garden City, United Kingdom

M

Marcus Lefebure

17BeOne Medicines Ltd, London, United Kingdom

M

Maria Thadani-Mulero

11Roche Products Ltd, Welwyn Garden City, United Kingdom

M

Michelle Boyer

12Genentech, Inc, South San Francisco, CA

J

John F. Seymour

Department of Haematology, Royal Melbourne Hospital and Peter MacCallum Cancer Centre, Melbourne, VIC, Australia