Evidence map›Paper›PMID 34793256›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2022

Venetoclax in Previously Treated Waldenström Macroglobulinemia.

Jorge J Castillo, John N Allan, Tanya Siddiqi, Ranjana H Advani, Kirsten Meid, Carly Leventoff, Timothy P White, Catherine A Flynn, Shayna Sarosiek, Andrew R Branagan and 13 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02677324 (Phase II Study of ABT-199), which is not on this map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
8.4field-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.

NCT02677324 phase2completednot on this map

Phase II Study of ABT-199 (GDC-199) In Patients With Relapsed Or Refractory Waldenström Macroglobulinemia

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2016 to 2022Enrolled33ConditionsWaldenstrom MacroglobulinemiaArmsABT199
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. The Direction of Modern Therapies in Waldenström Macroglobulinaemia.Journal of cellular and molecular medicine · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Waldenström Macroglobulinemia - A State-of-the-Art Review: Part 2- Focus on Therapy.Mediterranean journal of hematology and infectious diseases · 2025
    Review
  19. Review
  20. Article
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

23 authors at 5 institutions in 1 country.

Jorge J CastilloBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-9490-7532
John N AllanNew York-Presbyterian Hospital, Weill Cornell Medical College, New York, NY.
Tanya SiddiqiCity of Hope National Medical Center, Duarte, CA.ORCID 0000-0001-5292-8298
Ranjana H AdvaniStanford Cancer Institute, Stanford University, Stanford, CA.ORCID 0000-0002-3219-2292
Kirsten MeidBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Carly LeventoffBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-3703-3901
Timothy P WhiteBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Catherine A FlynnBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Shayna SarosiekBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-0075-6735
Andrew R BranaganHarvard Medical School, Boston, MA.ORCID 0000-0002-3868-9267
Maria G DemosBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Maria L GuerreraBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Amanda KofidesBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Xia LiuBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Manit MunshiBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Nicholas TsakmaklisBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Lian XuBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Guang YangBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-3049-4200
Christopher J PattersonBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.
Zachary R HunterBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1689-1691
Matthew S DavidsHarvard Medical School, Boston, MA.ORCID 0000-0003-4529-2003
Richard R FurmanNew York-Presbyterian Hospital, Weill Cornell Medical College, New York, NY.ORCID 0000-0003-1677-7626
Steven P TreonBing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-6393-6154
Dana-Farber Cancer Institute · USHarvard University · USNewYork–Presbyterian Hospital · USCity Of Hope National Medical Center · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBCL2 is overexpressed and confers prosurvival signaling in malignant lymphoplasmacytic cells in Waldenström macroglobulinemia (WM). Venetoclax is a potent BCL2 antagonist and triggers in vitro apoptosis of WM cells. The activity of venetoclax in WM remains to be clarified. PATIENTS AND

methodsWe performed a multicenter, prospective phase II study of venetoclax in patients with previously treated WM (NCT02677324). Venetoclax was dose-escalated from 200 mg to a maximum dose of 800 mg daily for up to 2 years.

resultsThirty-two patients were evaluable, including 16 previously exposed to Bruton tyrosine kinase inhibitors (BTKis). All patients were

conclusionVenetoclax is safe and highly active in patients with previously treated WM, including those who previously received BTKis.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsBiomarkers, TumorBridged Bicyclo Compounds, HeterocyclicDisease ProgressionFemaleHumansMaleMiddle AgedMutationMyeloid Differentiation Factor 88Progression-Free SurvivalProspective StudiesProto-Oncogene Proteins c-bcl-2Antineoplastic AgentsBCL2 protein, humanBiomarkers, TumorBridged Bicyclo Compounds, HeterocyclicCXCR4 protein, humanMYD88 protein, humanMyeloid Differentiation Factor 88Proto-Oncogene Proteins c-bcl-2Receptors, CXCR4Sulfonamidesvenetoclax

Identifiers

PMID34793256
PMCPMC8683218
OpenAlexW3212903318

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.