Evidence map›Paper›PMID 31900407›Full record

ArticleLeukemia2020

Immunomodulation with pomalidomide at early lymphocyte recovery after induction chemotherapy in newly diagnosed AML and high-risk MDS.

Joshua F Zeidner, Hanna A Knaus, Amer M Zeidan, Amanda L Blackford, Raul Montiel-Esparza, Hubert Hackl, Gabrielle T Prince, Lukasz P Gondek, Gabriel Ghiaur, Margaret M Showel and 11 more

Open access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Leukemia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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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

21 authors at 5 institutions in 2 countries.

Joshua F Zeidner *University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.ORCID http://orcid.org/0000-0002-9014-1514
Hanna A Knaus *Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Amer M ZeidanYale Cancer Center, New Haven, CT, USA.
Amanda L BlackfordSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Raul Montiel-EsparzaSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Hubert HacklDivision of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-4055-3841
Gabrielle T PrinceSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Lukasz P GondekSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Gabriel GhiaurSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Margaret M ShowelSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Amy E DeZernSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Keith W PratzSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
B Douglas SmithSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Mark J LevisSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-0473-6982
Steven GoreYale Cancer Center, New Haven, CT, USA.
Catherine C CoombsUniversity of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.
Matthew C FosterUniversity of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.
Howard StreicherNational Cancer Institute, Rockville, MD, USA.
Judith E KarpSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Leo LuznikSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Ivana GojoSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA. igojo1@jhmi.edu.
Johns Hopkins University · USUniversity of North Carolina at Chapel Hill · USYale Cancer Center · USInnsbruck Medical University · ATNational Cancer Institute · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
ViKTriY-PC Consortium Phase II SupplementUM1CA186689 · NCI · YALE UNIVERSITY · PI Patricia M. LoRusso · 2014 to 2026
$22.2M
The Johns Hopkins Translational Science Team for the ET-CTNUM1CA186691 · NCI · JOHNS HOPKINS UNIVERSITY · PI Jan Hendrik Beumer, Michael A Carducci · 2014 to 2026
$21.9M
UM1 Supplement for Early Therapeutic Trials with Phase 2 IntentUM1CA186712 · NCI · OHIO STATE UNIVERSITY · PI SUSANNE M ARNOLD, WILLIAM E. CARSON · 2014 to 2026
$19.3M
UNC Oncology K12K12CA120780 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WILLIAM Y. KIM · 2007 to 2026
$9.6M
Duke-UNC-Wash U Partnership for Early Phase Clinical Trials in CancerUM1CA186704 · NCI · DUKE UNIVERSITY · PI ABBRUZZESE, JAMES L., DEES, ELIZABETH CLAIRE · 2014 to 2019
$6.8M
Wisconsin and New Jersey Alliance in Precision Experimental TherapeuticsUM1CA186716 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI JABBOUR, SALMA, LIU, GLENN · 2014 to 2019
$4.1M
Hedgehog Signaling in the Progression of Myelodysplastic SyndromesK08HL136894 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI GONDEK, LUKASZ PAWEL · 2017 to 2021
$859k
NCATS NIH HHS UL1 TR001863NCI NIH HHS K12 CA120780NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA016359NCI NIH HHS UM1 CA186689NCI NIH HHS UM1 CA186691NCI NIH HHS UM1 CA186704NCI NIH HHS UM1 CA186712NCI NIH HHS UM1 CA186716NHLBI NIH HHS K08 HL136894
6 · The paper itself

Abstract

An immunosuppressive microenvironment promoting leukemia cell immune escape plays an important role in the pathogenesis of AML. Through its interaction with cereblon, a substrate receptor for the E3 ubiquitin ligase complex, pomalidomide leads to selective ubiquitination of transcription factors Aiolos and Ikaros thereby promoting immune modulation. In this phase I trial, 51 newly diagnosed non-favorable risk AML and high-risk MDS patients were enrolled and treated with AcDVP16 (cytarabine 667 mg/m

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsCytarabineDisease-Free SurvivalEtoposideFemaleHexosaminesHumansImmunologic FactorsImmunomodulationInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMaximum Tolerated DoseMiddle AgedCytarabinedaunosamineEtoposideHexosaminesImmunologic FactorspomalidomideThalidomide

Identifiers

PMID31900407
PMCPMC7272276
OpenAlexW2998293013

What OpenQuestion holds

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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.