Evidence map›Paper›PMID 32986498›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Venetoclax Plus Rituximab in Relapsed Chronic Lymphocytic Leukemia: 4-Year Results and Evaluation of Impact of Genomic Complexity and Gene Mutations From the MURANO Phase III Study.

Arnon P Kater, Jenny Qun Wu, Thomas Kipps, Barbara Eichhorst, Peter Hillmen, James D'Rozario, Sarit Assouline, Carolyn Owen, Tadeusz Robak, Javier de la Serna and 18 more

Open access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 2 pooled it
18.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

128 citing papers in PubMed, 2 syntheses or guidelines pooled it, 215 citations in OpenAlex.

  1. Guideline
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  7. Minimal Residual Disease Dynamics after Venetoclax-Obinutuzumab Treatment: Extended Off-Treatment Follow-up From the Randomized CLL14 Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
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  10. Refined Continuous Risk Index for Accurately Predicting Outcomes of Patients With Chronic Lymphocytic Leukemia After Limited-Duration Therapy.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
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68 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 15 institutions in 11 countries.

Arnon P KaterDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Academic Medical Center, on behalf of Hovon Chronic Lymphocytic Leukemia Working Group, Amsterdam, the Netherlands.ORCID 0000-0003-3190-1891
Jenny Qun WuGenentech, South San Francisco, CA.
Thomas KippsUniversity of California School of Medicine, San Diego, CA.ORCID 0000-0002-0064-4549
Barbara EichhorstUniversity of Cologne, Cologne, Germany.
Peter HillmenSt James's University Hospital, Leeds, United Kingdom.ORCID 0000-0001-5617-4403
James D'RozarioThe John Curtin School of Medical Research, Australian National University, Canberra, Australia.
Sarit AssoulineSegal Cancer Center, Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada.ORCID 0000-0002-7638-1589
Carolyn OwenUniversity of Calgary, Calgary, Alberta, Canada.
Tadeusz RobakMedical University of Lodz, Copernicus Memorial Hospital, Lodz, Poland.
Javier de la SernaHospital Universitario 12 de Octubre, Madrid, Spain.ORCID 0000-0003-3904-1101
Ulrich JaegerDivision of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Guillaume CartronDepartment of Clinical Hematology, University Hospital Montpellier, Montpellier, France.
Marco MontilloDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Julie DuboisDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Academic Medical Center, on behalf of Hovon Chronic Lymphocytic Leukemia Working Group, Amsterdam, the Netherlands.
Eric ElderingDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Academic Medical Center, on behalf of Hovon Chronic Lymphocytic Leukemia Working Group, Amsterdam, the Netherlands.ORCID 0000-0003-0561-6640
Clemens MellinkDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Academic Medical Center, on behalf of Hovon Chronic Lymphocytic Leukemia Working Group, Amsterdam, the Netherlands.
Anne-Marie Van Der Kevie-KersemaekersDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Academic Medical Center, on behalf of Hovon Chronic Lymphocytic Leukemia Working Group, Amsterdam, the Netherlands.ORCID 0000-0003-3515-6198
Su Young KimAbbVie, Chicago, IL.
Brenda ChylaAbbVie, Chicago, IL.
Elizabeth PunnooseGenentech, South San Francisco, CA.
Christopher R BolenGenentech, South San Francisco, CA.
Zoe June AssafGenentech, South San Francisco, CA.
Yanwen JiangGenentech, South San Francisco, CA.
Jue WangGenentech, South San Francisco, CA.
Marcus LefebureRoche Products Limited, Welwyn Garden City, United Kingdom.
Michelle BoyerRoche Products Limited, Welwyn Garden City, United Kingdom.
Kathryn HumphreyRoche Products Limited, Welwyn Garden City, United Kingdom.
John F SeymourRoyal Melbourne Hospital, Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Victoria, Australia.ORCID 0000-0003-2188-6835
Amsterdam UMC Location University of Amsterdam · NLRoche (United Kingdom) · GBAbbVie (United States) · USAustralian National University · AUAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITCentre Hospitalier Universitaire de Montpellier · FRCopernicus Memorial Hospital · PLHospital Universitario 12 De Octubre · ESJewish General Hospital · CAMedical University of Vienna · ATSt James's University Hospital · GBThe Royal Melbourne Hospital · AUUniversity of Calgary · CAUniversity of California San Diego · USUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn previous analyses of the MURANO study, fixed-duration venetoclax plus rituximab (VenR) resulted in improved progression-free survival (PFS) compared with bendamustine plus rituximab (BR) in patients with relapsed or refractory chronic lymphocytic leukemia (CLL). At the 4-year follow-up, we report long-term outcomes, response to subsequent therapies, and the predictive value of molecular and genetic characteristics. PATIENTS AND

methodsPatients with CLL were randomly assigned to 2 years of venetoclax (VenR for the first six cycles) or six cycles of BR. PFS, overall survival (OS), peripheral-blood minimal residual disease (MRD) status, genomic complexity (GC), and gene mutations were assessed.

resultsOf 389 patients, 194 were assigned to VenR and 195 to BR. Four-year PFS and OS rates were higher with VenR than BR, at 57.3% and 4.6% (hazard ratio [HR], 0.19; 95% CI, 0.14 to 0.25), and 85.3% and 66.8% (HR, 0.41; 95% CI, 0.26 to 0.65), respectively. Undetectable MRD (uMRD) at end of combination therapy (EOCT) was associated with superior PFS compared with low MRD positivity (HR, 0.50) and high MRD positivity (HR, 0.15). Patients in the VenR arm who received ibrutinib as their first therapy after progression (n = 12) had a reported response rate of 100% (10 of 10 evaluable patients); patients subsequently treated with a venetoclax-based regimen (n = 14) had a reported response rate of 55% (six of 11 evaluable patients). With VenR, the uMRD rate at end of treatment (EOT) was lower in patients with GC than in those without GC (

conclusionEfficacy benefits with fixed-duration VenR are sustained and particularly durable in patients who achieve uMRD. Salvage therapy with ibrutinib after VenR achieved high response rates. Genetic mutations and GC affected MRD rates and PFS.

Indexed as

MutationAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBridged Bicyclo Compounds, HeterocyclicExportin 1 ProteinFollow-Up StudiesHumansKaplan-Meier EstimateKaryopherinsLeukemia, Lymphocytic, Chronic, B-CellProgression-Free SurvivalProto-Oncogene Proteins B-rafReceptor, Notch1Receptors, Cytoplasmic and NuclearRituximabSulfonamidesBiomarkers, TumorBRAF protein, humanBridged Bicyclo Compounds, HeterocyclicExportin 1 ProteinKaryopherinsNOTCH1 protein, humanProto-Oncogene Proteins B-rafReceptor, Notch1Receptors, Cytoplasmic and NuclearRituximabSulfonamidesTP53 protein, humanTumor Suppressor Protein p53venetoclax

Identifiers

PMID32986498
PMCPMC7768340
OpenAlexW3088078660

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.