Evidence map›Paper›PMID 34156898›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia.

Pinkal M Desai, Janice Brown, Saar Gill, Melham M Solh, Luke P Akard, Jack W Hsu, Celalettin Ustun, Charalambos Andreadis, Olga Frankfurt, James M Foran and 22 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Article
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  8. Article
  9. Current state and future opportunities in granulocyte colony-stimulating factor (G-CSF).Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
    Article
  10. Article
  11. Review
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

32 authors at 20 institutions in 1 country.

Pinkal M DesaiWeill Cornell Medical College, New York, NY.ORCID 0000-0002-9816-7284
Janice BrownStanford University Medical Center, Stanford, CA.
Saar GillUniversity of Pennsylvania, Philadelphia, PA.ORCID 0000-0001-7946-7778
Melham M SolhNorthside Hospital, Atlanta, GA.ORCID 0000-0003-3766-5623
Luke P AkardIndiana Blood and Marrow Transplantation, Indianapolis, IN.
Jack W HsuUniversity of Florida, Gainesville, FL.
Celalettin UstunUniversity of Minnesota, St Paul, MN.
Charalambos AndreadisUniversity of California San Francisco, San Francisco, CA.
Olga FrankfurtNorthwestern University, Chicago, IL.
James M ForanMayo Clinic, Jacksonville, FL.
John ListerAllegheny Health Network, Pittsburgh, PA.ORCID 0000-0002-5333-099X
Gary J SchillerDavid Geffen School of Medicine at UCLA, Los Angeles, CA.
Matthew J WieduwiltStephenson Cancer Center, University of Oklahoma, Oklahoma City, OK.ORCID 0000-0002-5414-9228
John M PagelSwedish Cancer Institute, Seattle, WA.ORCID 0000-0001-5745-8125
Patrick J StiffLoyola University Stritch School of Medicine, Maywood, IL.ORCID 0000-0001-8265-9340
Delong LiuNew York Medical College, Hawthorne, NY.
Irum KhanUniversity of Illinois Cancer Center, Chicago, IL.ORCID 0000-0003-1855-7731
Wendy StockUniversity of Chicago, Chicago, IL.ORCID 0000-0002-8349-9200
Suman KambhampatiKansas City Veterans Affairs Medical Center, Kansas City, MO.
Martin S TallmanMemorial Sloan Kettering Cancer Center, New York, NY.
Lawrence MorrisNorthside Hospital, Atlanta, GA.
John EdwardsIndiana Blood and Marrow Transplantation, Indianapolis, IN.ORCID 0000-0003-0345-2654
Iskra PusicWashington University, St Louis, MO.
Hagop M KantarjianThe University of Texas MD Anderson Cancer Center, Houston, TX.
Richard MamelokCellerant Therapeutics, San Carlos, CA.
Alicia WongCellerant Therapeutics, San Carlos, CA.
Rodney Van SyocCellerant Therapeutics, San Carlos, CA.
Lois KellermanCellerant Therapeutics, San Carlos, CA.
Swapna PanugantiCellerant Therapeutics, San Carlos, CA.
Ramkumar MandalamCellerant Therapeutics, San Carlos, CA.
Camille N AbboudWashington University, St Louis, MO.ORCID 0000-0002-5469-8534
Farhad RavandiThe University of Texas MD Anderson Cancer Center, Houston, TX.
Cellerant Therapeutics (United States) · USIndiana Cancer Consortium · USNorthside Hospital · USThe University of Texas MD Anderson Cancer Center · USWashington University in St. Louis · USAllegheny Health Network · USCornell University · USJacksonville College · USLoyola University Chicago · USMemorial Sloan Kettering Cancer Center · USNew York Medical College · USNorthwestern University · USOklahoma State University Oklahoma City · USStanford Medicine · USUniversity of California, Los Angeles · USUniversity of California, San Francisco · USUniversity of Chicago · USUniversity of Florida · USUniversity of Illinois Chicago · USUniversity of Minnesota · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Institutional Career DevelopmentKL2TR002002 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PHILLIPS, SHANE A · 2016 to 2024
$6.8M
NCATS NIH HHS KL2 TR002002NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeStandard cytotoxic induction chemotherapy for acute myeloid leukemia (AML) results in prolonged neutropenia and risk of infection. Romyelocel-L is a universal, allogeneic myeloid progenitor cell product being studied to reduce infection during induction chemotherapy. PATIENTS AND

methodsOne hundred sixty-three patients with de novo AML (age ≥ 55 years) receiving induction chemotherapy were randomly assigned on day 0 (d0), of whom 120 were evaluable. Subjects received either romyelocel-L infusion on d9 with granulocyte colony-stimulating factor (G-CSF) starting daily d14 (treatment group) or G-CSF daily alone on d14 (control) until absolute neutrophil count recovery to 500/µL. End points included days in febrile episode, microbiologically defined infections, clinically diagnosed infection, and days in hospital.

resultsMean days in febrile episode was shorter in the treatment arm from d15 through d28 (2.36

conclusionSubjects receiving romyelocel-L showed a decreased incidence of infections, antimicrobial use, and hospitalization, suggesting that romyelocel-L may provide a new option to reduce infections in patients with AML undergoing induction therapy.

Indexed as

AdultAgedAntifungal AgentsFemaleGranulocyte Colony-Stimulating FactorHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMiddle AgedMyeloid Progenitor CellsNeutrophilsProspective StudiesAntifungal AgentsGranulocyte Colony-Stimulating Factor

Identifiers

PMID34156898
PMCPMC8500663
OpenAlexW3175145807

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.