Evidence map›Paper›PMID 41899494›Full record

ReviewCancers2026

Biological Advances and Current Challenges for Pediatric Rhabdomyosarcoma.

Katie E Hebron, Patience Odeniyide, Yun Wei, Berkley E Gryder, Frederic G Barr, Dana L Casey, Eleanor Y Chen, Brian D Crompton, Filemon S Dela Cruz, Adam D Durbin and 30 more

Abstract readReview
In one paragraph

Review in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

40 authors.

Katie E HebronLaboratory of Cell and Developmental Signaling, National Cancer Institute at Frederick, National Institutes of Health, Frederick, MD 21701, USA.ORCID 0000-0002-4740-8930
Patience OdeniyideDivision of Pediatric Oncology, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-9783-1657
Yun WeiMolecular Pathology Unit, Massachusetts General Research Institute, Harvard Medical School, Charlestown, MA 02129, USA.ORCID 0000-0003-2080-499X
Berkley E GryderDepartment of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.ORCID 0000-0003-0130-2302
Frederic G BarrLaboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA.
Dana L CaseyDepartment of Radiation Oncology, University of North Carolina School of Medicine, Chapel Hill, NC 27514, USA.
Eleanor Y ChenDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98115, USA.ORCID 0000-0003-4372-7560
Brian D CromptonDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Filemon S Dela CruzDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0002-8356-5191
Adam D DurbinDivision of Molecular Oncology, Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-5472-9847
Heide L FordDepartment of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Susanne A GatzDepartment of Cancer and Genomic Sciences, School of Medical Sciences, College of Medicine and Health, University of Birmingham, Birmingham B15 2TT, UK.ORCID 0000-0002-6438-9778
Mark E HatleyDivision of Molecular Oncology, Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0001-7147-3946
Anton G HenssenCharité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Germany, Department of Pediatric Hematology and Oncology, Augustenburger Platz, 13353 Berlin, Germany.
Simone HettmerUniversity Medicine Halle, Pediatrics, Martin Luther University Halle, 06108 Halle, Germany.ORCID 0000-0003-1709-4448
Peter J HoughtonGreehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, TX 78229, USA.
Genevieve C KendallCenter for Childhood Cancer Research, Nationwide Children's Hospital, Columbus, OH 43205, USA.ORCID 0000-0003-3775-2006
Javed KhanGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-5858-0488
Philip J LupoDivision of Hematology/Oncology, Department of Pediatrics, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0003-0978-5863
Anand G PatelDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-1438-8275
Silvia PomellaDepartment of Hematology and Oncology, Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-7007-4238
Rossella RotaDepartment of Hematology and Oncology, Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-9408-7711
Marco SchitoUGenome AI, Tucson, AZ 85614, USA.
Reineke A SchootPrincess Máxima Center, 3584 CS Utrecht, The Netherlands.
Jack F ShernPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0001-5579-7625
Benjamin Z StantonCenter for Childhood Cancer Research, Nationwide Children's Hospital, Columbus, OH 43205, USA.ORCID 0000-0002-2613-2955
Elizabeth A StewartDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Cathy A SwindlehurstKatalytic Therapeutics, San Diego, CA 92126, USA.
Craig J ThomasDivision of Pre-Clinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, MD 20850, USA.
Christopher R VakocCold Spring Harbor Laboratory, New York, NY 11724, USA.
Angelina V VasevaDepartment of Pediatrics, School of Medicine, Oregon Health and Science University, Portland, OR 97239, USA.
Rajkumar VenkatramaniDepartment of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX 77030, USA.
Leonard H WexlerDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Jason T YusteinWinship Cancer Institute and Aflac Cancer and Blood Disorders Center, Emory University, Atlanta, GA 30322, USA.
Sharon HammondSummer's Way Foundation, Centennial, CO 80016, USA.
Christine M HeskePediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0003-0956-6249
David M LangenauMolecular Pathology Unit, Massachusetts General Research Institute, Harvard Medical School, Charlestown, MA 02129, USA.
Corinne M LinardicDivision of Hematology-Oncology, Department of Pediatrics, Duke University School of Medicine, Durham, NC 27701, USA.ORCID 0000-0002-3257-2885
Myron S IgnatiusGreehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, TX 78229, USA.
Marielle E YoheLaboratory of Cell and Developmental Signaling, National Cancer Institute at Frederick, National Institutes of Health, Frederick, MD 21701, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
LAB RESEARCH TRAINING IN PEDIATRIC ONCOLOGY-HEMATOLOGYT32CA060441 · NCI · JOHNS HOPKINS UNIVERSITY · PI ALAN D FRIEDMAN · 1993 to 2026
$14.9M
Targeting mutant-MYOD1 driven rhabdomyosarcomaU01CA298763 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Benjamin Stanton · 2025 to 2026
$853k
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA060441NCI NIH HHS U01 CA298763
6 · The paper itself

Abstract

Despite comprehensive and multi-modal therapy, outcomes for children and adolescents with rhabdomyosarcoma (RMS) have plateaued over the past four decades. This is not for a lack of progress in the basic and translational studies of RMS. Indeed, advances in animal models and/or patient tissue sample acquisition and analysis have improved our understanding of RMS biology. Large-scale sequencing efforts have generated transcriptomic, genomic, and epigenomic datasets that highlight the heterogeneity of RMS and have the potential to improve prognostication and the application of precision medicine in patients with RMS. However, few of these discoveries have been clinically translated, and limitations to the accessibility, uniformity, and application of these new models and datasets hinder their utility. Here, we discuss how advances in understanding RMS biology, optimization of preclinical models, and strategies for translating basic science discoveries to the clinic can potentially improve outcomes for patients with RMS.

Indexed as

animal modelscells of originpediatric sarcomaskeletal muscle malignancytumor heterogeneity

Identifiers

PMID41899494
PMCPMC13023981

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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.