Evidence map›Paper›PMID 42636421›Full record

Observational studyJournal of clinical oncology : official journal of the American Society of Clinical Oncology2026

Omitting Bone Marrow Sampling in FDG-Avid Rhabdomyosarcoma With 2-[

Federico Mercolini, Marissa Just, Barry L Shulkin, Natalie B Collins, Jacquelyn Crane, Douglas Harrison, Maria C Affinita, Wendy Allen-Rhoades, Alessandra Alessi, Sebastian D Asaftei and 27 more

Erratum issuedAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

5 · Who and what money

Authors and funding

37 authors.

Federico MercoliniPediatric Hematology and Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID 0000-0001-9932-1944
Marissa JustDepartment of Pediatric Hematology/Oncology/Stem Cell Transplant, Indiana University, Indianapolis, IN.
Barry L ShulkinDepartment of Radiology, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0003-4784-7914
Natalie B CollinsDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.ORCID 0000-0003-2980-9244
Jacquelyn CranePediatric Hematology/ Oncology/ Stem Cell Transplantation and Regenerative Medicine, Stanford Medicine, Stanford, CA.
Douglas HarrisonDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX.
Maria C AffinitaPediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy.
Wendy Allen-RhoadesMayo Clinic Comprehensive Cancer Center, Rochester, MN.
Alessandra AlessiNuclear Medicine, IRCCS Foundation, National Institute of Tumor, Milan, Italy.ORCID 0000-0003-3853-1926
Sebastian D AsafteiDepartment of Pediatric Hematology and Oncology, University Children's Hospital "Regina Margherita", Turin, Italy.ORCID 0000-0002-3890-1686
Michael A ArnoldDepartment of Pathology and Laboratory Medicine, Children's Hospital Colorado and Department of Pathology, University of Colorado, Aurora, CO.ORCID 0000-0002-6921-3720
Sonja ChenDepartment of Pathology and Laboratory Medicine, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH.ORCID 0000-0001-6174-8723
Stefano ChiaravalliPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Forrest FitzGeraldMassachusetts Institute of Technology, Cambridge, MA.ORCID 0000-0003-3568-6543
Martin T FreitagDepartment of Nuclear Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-2116-6873
Jessica L IftnerDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Hedieh KhalatbariTexas Scottish Rite Hospital for Children, Dallas, TX.
Bart de KeizerPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-6270-9483
Irene von LuettichauDepartment of Pediatrics, Children's Cancer Research Center, Kinderklinik München Schwabing, TUM School of Medicine and Health, Technical University of Munich, Munich, Germany.
Christine Mauz-KörholzDepartment of Pediatric Hematology, Oncology and Immunodeficiencies, Justus-Liebig-University, Gießen, Germany.ORCID 0000-0002-8205-8665
Claudia RossigUniversity Children's Hospital Muenster, Muenster, Germany.ORCID 0000-0002-8672-5285
Guido RoveraDepartment of Medical Sciences, University of Turin, Turin, Italy.ORCID 0000-0003-1839-0206
Stefan RutkowskiDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5446-9571
Justin B SimsDepartment of Radiology, Indiana University, Indianapolis, IN.
Stephan D VossDepartment of Radiology, Children's Hospital Boston and Harvard Medical School, Boston, MA.ORCID 0000-0002-2092-2219
Ayami YoshimiDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Suzi BirzDepartment of Pediatrics, University of Chicago, Chicago, IL.ORCID 0000-0002-9512-799X
Gianni BisognoPediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy.ORCID 0000-0003-4462-5523
Martin EbingerDepartment of Pediatric Hematology and Oncology, University Children's Hospital, Tübingen, Germany.ORCID 0000-0002-4229-8058
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0001-7659-1028
Monika Sparber-SauerDepartment of Pediatric Hematology and Oncology, University Children's Hospital, Tübingen, Germany.ORCID 0000-0001-9551-2399
Bernhard HallerInstitute of AI and Informatics in Medicine, TUM School of Medicine and Health, Technical University München, München, Germany.ORCID 0000-0002-9723-393X
Aaron R WeissMaineHealth Maine Medical Center, Portland, ME.ORCID 0000-0001-8352-3963
Corinne M LinardicDepartments of Pediatrics and Pharmacology & Cancer Biology, Duke University School of Medicine, Durham, NC.ORCID 0000-0002-3257-2885
Reineke A SchootPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-8838-981X
Simone HettmerDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0003-1709-4448
INSTRuCT Imaging/Pathology/Biology Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDetection of bone marrow disease has been a major component of rhabdomyosarcoma (RMS) staging with bilateral bone marrow aspirates/biopsies (BMAB) from the iliac crests considered the diagnostic gold standard. This study's goal was to determine if 2-

methodsPatients were recruited in Europe and North America. Medical records, FDG PET/CT or FDG PET/MRI (PET), and BMAB reports were collected retrospectively. Images were re-reviewed by nuclear medicine physicians at the patients' home institutions if PET reports indicated increased FDG uptake at bone/bone marrow sites or if tumor cells were detected in bone marrow samples.

resultsPET imaging and BMAB were performed before chemotherapy and tumor resection in 301 patients with FDG-avid RMS. Bone marrow metastases were detected by PET and BMAB in 54, by PET only in 24, and by BMAB only in one of 301 patients with FDG-avid primary tumors. Absence of bone marrow metastases was confirmed by PET and BMAB in 222 of 301 patients. These observations translated into 98% sensitivity and 90% specificity for PET in detecting bone marrow metastases when BMAB was considered as gold standard. FDG-avid marrow disease was patchy (1-5 foci) in one third of cases. Patients with marrow disease indicated by PET and BMAB had more FDG-avid bone marrow foci, more metastatic sites, and lower survival than those with marrow disease indicated by PET only, suggesting more advanced disease stages.

conclusionBone marrow sampling may be omitted in patients without evidence of FDG-avid bone marrow disease by PET. If there are FDG-avid bone marrow lesions, further investigation by MRI and/or biopsy should be considered.

Indexed as

Bone MarrowBone Marrow NeoplasmsFluorodeoxyglucose F18Positron Emission Tomography Computed TomographyRadiopharmaceuticalsRhabdomyosarcomaAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantMagnetic Resonance ImagingMaleFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID42636421
PMCPMC13668043

What OpenQuestion holds

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