Evidence map›Paper›PMID 36809796›Full record

ArticleBlood advances2023

A multicenter analysis of the outcomes with venetoclax in patients with relapsed mantle cell lymphoma.

Yazeed Sawalha, Subir Goyal, Jeffrey M Switchenko, Jason T Romancik, Manali Kamdar, I Brian Greenwell, Brian T Hess, Krista M Isaac, Craig A Portell, Alex Mejia Garcia and 12 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

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  4. Advances in targeted and cellular therapies for relapsed/refractory mantle cell lymphoma: immunotherapeutic strategies and challenges.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

22 authors at 13 institutions in 1 country.

Yazeed SawalhaDivision of Hematology, The Ohio State University, Columbus, OH.ORCID 0000-0001-6355-3671
Subir GoyalBiostatistics Shared Resource, Winship Cancer Institute, Emory University, Atlanta, GA.
Jeffrey M SwitchenkoBiostatistics Shared Resource, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-5563-9325
Jason T RomancikDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0003-0054-9362
Manali KamdarDivision of Hematology, University of Colorado Denver, Denver, CO.
I Brian GreenwellDivision of Hematology and Oncology, Medical University of South Carolina, Charleston, SC.ORCID 0000-0003-2752-8078
Brian T HessDivision of Hematology and Oncology, Medical University of South Carolina, Charleston, SC.
Krista M IsaacDivision of Hematology/Oncology, University of Virginia, Charlottesville, VA.ORCID 0000-0002-0234-139X
Craig A PortellDivision of Hematology/Oncology, University of Virginia, Charlottesville, VA.ORCID 0000-0002-9487-8345
Alex Mejia GarciaMiami Cancer Institute, Miami, FL.
Scott GoldsmithDepartment of Medicine, Washington University School of Medicine, Washington University, St. Louis, MO.
Natalie S GroverThe University of North Carolina, Chapel Hill, NC.
Peter A RiedellSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL.ORCID 0000-0003-2719-0580
Reem KarmaliDivision of Hematology and Oncology, Northwestern University, Chicago, IL.ORCID 0000-0003-0984-4376
Madelyn BurkartDivision of Hematology and Oncology, Northwestern University, Chicago, IL.ORCID 0000-0002-5105-0564
Michael BuegeLymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-9063-1495
Othman AkhtarRoswell Park Comprehensive Cancer Center, Buffalo, NY.
Pallawi TorkaRoswell Park Comprehensive Cancer Center, Buffalo, NY.ORCID 0000-0002-1681-5883
Anita KumarLymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1381-5810
Brian T HillDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.
Brad S KahlDepartment of Medicine, Washington University School of Medicine, Washington University, St. Louis, MO.ORCID 0000-0003-0459-6609
Jonathon B CohenDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-2723-6481
Emory University · USMedical University of South Carolina · USMemorial Sloan Kettering Cancer Center · USNorthwestern University · USRoswell Park Comprehensive Cancer Center · USUniversity of Virginia · USWashington University in St. Louis · USCancer Institute of Florida · USCleveland Clinic · USThe Ohio State University · USUniversity of Chicago · USUniversity of Colorado Denver · USUniversity of North Carolina at Chapel Hill · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
NCATS NIH HHS UL1 TR002733NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA138292
6 · The paper itself

Abstract

To report the activity of venetoclax in patients with relapsed mantle cell lymphoma (MCL), we identified 81 patients treated with venetoclax monotherapy (n = 50, 62%) or in combination with a Bruton tyrosine kinase inhibitor (BTKi) (n = 16, 20%), an anti-CD20 monoclonal antibody (n = 11, 14%), or other active agents at 12 US academic medical centers. Patients had high-risk disease features including Ki67 >30% (61%), blastoid/pleomorphic histology (29%), complex karyotype (34%), and TP53 alterations (49%), and received a median of 3 prior treatments including BTKis in 91%. Venetoclax alone or in combination resulted in an overall response rate (ORR) of 40% and median progression-free (PFS) and overall survival (OS) of 3.7 and 12.5 months, respectively. The receipt of ≤3 prior treatments was associated with higher odds of response to venetoclax in a univariable analysis. In a multivariable analysis, having a high-risk Mantle Cell Lymphoma International Prognostic Index score before receiving venetoclax and disease relapse or progression within 24 months of diagnosis were associated with inferior OS whereas the use of venetoclax in combination was associated with superior OS. Although most patients (61%) had low risk for tumor lysis syndrome (TLS), 12.3% of patients developed TLS despite the implementation of several mitigation strategies. In conclusion, venetoclax resulted in good ORR but short PFS in patients with MCL who are at high risk, and may have a better role in earlier lines of treatment and/or in conation with other active agents. TLS remains an important risk in patients with MCL who initiate treatment with venetoclax.

Indexed as

Antineoplastic AgentsLymphoma, Mantle-CellTumor Lysis SyndromeAdultBridged Bicyclo Compounds, HeterocyclicHumansNeoplasm Recurrence, LocalSulfonamidesAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclax

Identifiers

PMID36809796
PMCPMC10320213
OpenAlexW4321434567

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.