Evidence map›Paper›PMID 36309981›Full record

ArticleAmerican journal of hematology2023

A phase 1b study of venetoclax and azacitidine combination in patients with relapsed or refractory myelodysplastic syndromes.

Amer M Zeidan, Uma Borate, Daniel A Pollyea, Andrew M Brunner, Fernando Roncolato, Jacqueline S Garcia, Robin Filshie, Olatoyosi Odenike, Anne Marie Watson, Ravitharan Krishnadasan and 9 more

Open access · hybridAbstract readMulticenter StudyClinical Trial, Phase I
In one paragraph

Article in American journal of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
11.2field-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

44 citing papers in PubMed, 72 citations in OpenAlex.

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  7. Therapy of high-risk myelodysplastic syndromes.Bone marrow transplantation · 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

19 authors at 14 institutions in 2 countries.

Amer M ZeidanSection of Hematology, Department of Internal Medicine, Yale University and Yale Cancer Center, New Haven, Connecticut, USA.
Uma BorateDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon, USA.
Daniel A PollyeaDivision of Hematology, Department of Medicine, University of Colorado, Aurora, Colorado, USA.
Andrew M BrunnerCenter for Leukemia, Massachusetts General Hospital, Boston, Massachusetts, USA.
Fernando RoncolatoDepartment of Hematology, St George Hospital, Sydney, New South Wales, Australia.
Jacqueline S GarciaDepartment of Medicine, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.ORCID 0000-0003-2118-6302
Robin FilshieDepartment of Hematology, St Vincent's Hospital, Melbourne, Victoria, Australia.
Olatoyosi OdenikeSection of Hematology/Oncology, University of Chicago Medicine and Comprehensive Cancer Center, Chicago, Illinois, USA.
Anne Marie WatsonDepartment of Hematology, Liverpool Hospital, Sydney, New South Wales, Australia.
Ravitharan KrishnadasanDepartment of Hematology, University of Arizona Cancer Center, Tucson, Arizona, USA.
Ashish BajelDepartment of Clinical Hematology, Peter MacCallum Cancer Center and The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Kiran NaqviResearch and Development, Genentech Inc, South San Francisco, California, USA.
Jiuhong ZhaResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
Wei-Han ChengResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
Ying ZhouResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
David HoffmanResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
Jason G HarbResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
Jalaja PotluriResearch and Development, AbbVie Inc, North Chicago, Illinois, USA.
Guillermo Garcia-ManeroDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-3631-2482
AbbVie (United States) · USAcentech (United States) · USDana-Farber Cancer Institute · USLiverpool Hospital · AUMassachusetts General Hospital · USOregon Health & Science University · USSt George Hospital · AUSt Vincent's Hospital Melbourne · AUThe Royal Melbourne Hospital · AUThe University of Texas MD Anderson Cancer Center · USUniversity of Arizona · USUniversity of Chicago · USUniversity of Colorado Anschutz Medical Campus · USYale Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with relapsed/refractory (R/R) higher-risk myelodysplastic syndromes (MDS) have a dismal median overall survival (OS) after failing hypomethylating agent (HMA) treatment. There is no standard of care for patients after HMA therapy failure; hence, there is a critical need for effective therapeutic strategies. Herein, we present the safety and efficacy of venetoclax + azacitidine in patients with R/R MDS. This phase 1b, open-label, multicenter study enrolled patients ≥18 years. Patients were treated with escalating doses of oral venetoclax: 100, 200, or 400 mg daily for 14 days every 28-day cycle. Azacitidine was administered on Days 1-7 every cycle at 75 mg/m

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMyelodysplastic SyndromesAgedAzacitidineBridged Bicyclo Compounds, HeterocyclicFemaleHumansLeukemia, Myeloid, AcuteMaleNeutropeniaSulfonamidesTreatment OutcomeAzacitidineBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclax

Identifiers

PMID36309981
PMCPMC10100228
OpenAlexW4307628892

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.