Evidence map›Paper›PMID 36724417›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2023

Circulating Tumor DNA Is Prognostic in Intermediate-Risk Rhabdomyosarcoma: A Report From the Children's Oncology Group.

Samuel Abbou, Kelly Klega, Junko Tsuji, Mohammad Tanhaemami, David Hall, Donald A Barkauskas, Mark D Krailo, Carrie Cibulskis, Anwesha Nag, Aaron R Thorner and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Rhabdomyosarcoma in children and young adults.Virchows Archiv : an international journal of pathology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 3 countries.

Samuel AbbouDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.
Kelly KlegaDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0002-3424-2003
Junko TsujiBroad Institute of Harvard and MIT, Cambridge, MA.ORCID 0000-0003-0139-3750
Mohammad TanhaemamiDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0002-6498-1181
David HallQuadW-COG Childhood Sarcoma Biostatistics and Annotation Office, Children's Oncology Group, Monrovia, CA.ORCID 0000-0003-1257-2316
Donald A BarkauskasQuadW-COG Childhood Sarcoma Biostatistics and Annotation Office, Children's Oncology Group, Monrovia, CA.ORCID 0000-0002-2339-719X
Mark D KrailoQuadW-COG Childhood Sarcoma Biostatistics and Annotation Office, Children's Oncology Group, Monrovia, CA.
Carrie CibulskisBroad Institute of Harvard and MIT, Cambridge, MA.
Anwesha NagDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0002-1947-7429
Aaron R ThornerDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0002-9160-7881
Samuel PollockBroad Institute of Harvard and MIT, Cambridge, MA.ORCID 0000-0001-5173-5259
Alma Imamovic-TucoDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0003-4454-6868
Jack F ShernGenetics Branch, Oncogenomics Section, Center for Cancer Research, National Institutes of Health, Bethesda, MD.ORCID 0000-0001-5579-7625
Steven G DuBoisDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0003-0882-738X
Rajkumar VenkatramaniDivision of Hematology/Oncology, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX.ORCID 0000-0002-4785-106X
Douglas S HawkinsHematology/Oncology, Seattle Children's Hospital, Seattle, WA.ORCID 0000-0003-3602-1375
Brian D CromptonDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0001-9404-6621
Broad Institute · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USUniversity of Southern California · USAlbert Einstein College of Medicine · USBaylor College of Medicine · USInserm · FRNational Institutes of Health · USSeattle Children's Hospital · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
COG U24 Funding 2026-2027U24CA196173 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Mignon Lee-Cheun Loh, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$62.5M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA114766NCI NIH HHS U24 CA196173
6 · The paper itself

Abstract

purposeNovel biomarkers are needed to differentiate outcomes in intermediate-risk rhabdomyosarcoma (IR RMS). We sought to evaluate strategies for identifying circulating tumor DNA (ctDNA) in IR RMS and to determine whether ctDNA detection before therapy is associated with outcome. PATIENTS AND

methodsPretreatment serum and tumor samples were available from 124 patients with newly diagnosed IR RMS from the Children's Oncology Group biorepository, including 75 patients with fusion-negative rhabdomyosarcoma (FN-RMS) and 49 with fusion-positive rhabdomyosarcoma (FP-RMS) disease. We used ultralow passage whole-genome sequencing to detect copy number alterations and a new custom sequencing assay, Rhabdo-Seq, to detect rearrangements and single-nucleotide variants.

resultsWe found that ultralow passage whole-genome sequencing was a method applicable to ctDNA detection in all patients with FN-RMS and that ctDNA was detectable in 13 of 75 serum samples (17%). However, the use of Rhabdo-Seq in FN-RMS samples also identified single-nucleotide variants, such as

conclusionOur study demonstrates that baseline ctDNA detection is feasible and is prognostic in IR RMS.

Indexed as

Circulating Tumor DNARhabdomyosarcomaRhabdomyosarcoma, AlveolarBiomarkers, TumorChildHumansNucleotidesPrognosisBiomarkers, TumorCirculating Tumor DNANucleotides

Identifiers

PMID36724417
PMCPMC10150913
OpenAlexW4318767345

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.