Evidence map›Paper›PMID 39437708›Full record

Trial reportBlood2025

Zanubrutinib, obinutuzumab, and venetoclax for first-line treatment of mantle cell lymphoma with a TP53 mutation.

Anita Kumar, Jacob Soumerai, Jeremy S Abramson, Jeffrey A Barnes, Philip Caron, Shalini Chhabra, Maria Chabowska, Ahmet Dogan, Lorenzo Falchi, Clare Grieve and 18 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03824483 (Phase 2 Study of Zanubrutinib, Obinutuzumab, and Venetoclax in Previously Untreated Patients With Chronic Lymphocytic Leukemia), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT03824483 phase2recruitingnot on this map

Phase 2 Study of Zanubrutinib, Obinutuzumab, and Venetoclax in Previously Untreated Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) and Mantle Cell Lymphoma (MCL)

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2019 to 2027Enrolled230ConditionsChronic Lymphocytic Leukemia (CLL), Small Lymphocytic Leukemia (SLL)ArmsZanubrutinib, Obinutuzumab, Venetoclax
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  13. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
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  17. Journal of clinical medicine · 2025
    Article
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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

28 authors.

Anita KumarDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1381-5810
Jacob SoumeraiCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Jeremy S AbramsonCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0001-8467-9257
Jeffrey A BarnesCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-4867-1909
Philip CaronDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Shalini ChhabraDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1123-5783
Maria ChabowskaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Ahmet DoganDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-6576-5256
Lorenzo FalchiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Clare GrieveDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-2931-886X
J Erika HayduCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Patrick Connor JohnsonCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-3943-6608
Ashlee JosephDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1699-5666
Hailey E KellyCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Alyssa LabarreDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Jennifer Kimberly LueDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Rosalba MartignettiCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Joanna MiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Alison MoskowitzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Colette OwensDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Sean PlummerCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Madeline PuccioCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Gilles SallesDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-9541-8666
Venkatraman SeshanDepartment of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-9258-2698
Elizabeth SimkinsCenter for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Natalie SlupeDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Honglei ZhangDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY.
Andrew D ZelenetzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1403-6883

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

abstractTP53-mutant mantle cell lymphoma (MCL) is associated with poor survival outcomes with standard chemoimmunotherapy. We conducted a multicenter, phase 2 study of zanubrutinib, obinutuzumab, and venetoclax (BOVen) in untreated patients with MCL with a TP53 mutation. Patients initially received 160 mg zanubrutinib twice daily and obinutuzumab. Obinutuzumab at a dose of 1000 mg was given on cycle 1 day 1, 8, and 15, and on day 1 of cycles 2 to 8. After 2 cycles, venetoclax was added with weekly dose ramp-up to 400 mg daily. After 24 cycles, if patients were in complete remission with undetectable minimal residual disease (uMRD) using an immunosequencing assay, treatment was discontinued. The primary end point was met if ≥11 patients were progression free at 2 years. The study included 25 patients with untreated MCL with a TP53 mutation. The best overall response rate was 96% (24/25) and the complete response rate was 88% (22/25). Frequency of uMRD at a sensitivity level of 1 × 10-5 and uMRD at a sensitivity level of 1 × 10-6 at cycle 13 was 95% (18/19) and 84% (16/19), respectively. With a median follow-up of 28.2 months, the 2-year progression-free, disease-specific, and overall survival were 72%, 91%, and 76%, respectively. Common side effects were generally low grade and included diarrhea (64%), neutropenia (32%), and infusion-related reactions (24%). BOVen was well tolerated and met its primary efficacy end point in TP53-mutant MCL. These data support its use and ongoing evaluation. This trial was registered at www.ClinicalTrials.gov as #NCT03824483.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Mantle-CellMutationTumor Suppressor Protein p53AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedPiperidinesPyrazolesPyrimidinesAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicobinutuzumabPiperidinesPyrazolesPyrimidinesSulfonamidesTP53 protein, humanTumor Suppressor Protein p53venetoclaxzanubrutinib

Identifiers

PMID39437708
PMCPMC11826521

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Registered trials

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.