Evidence map›Paper›PMID 37916971›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2024

Translational Aspects of Epithelioid Sarcoma: Current Consensus.

Thomas G P Grünewald, Sophie Postel-Vinay, Robert T Nakayama, Noah E Berlow, Andrea Bolzicco, Vincenzo Cerullo, Josephine K Dermawan, Anna Maria Frezza, Antoine Italiano, Jia Xiang Jin and 16 more

Abstract readReviewConsensus Statement
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Article
  7. Review
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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

26 authors.

Thomas G P GrünewaldDivision of Translational Pediatric Sarcoma Research, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany.ORCID 0000-0003-0920-7377
Sophie Postel-VinayDépartement d'Innovation Thérapeutique et d'Essais Précoces (DITEP), Gustave Roussy, Université Paris Saclay, Villejuif, France.ORCID 0000-0001-5562-1857
Robert T NakayamaDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0003-1985-2169
Noah E BerlowChildren's Cancer Therapy Development Institute, Hillsboro, Oregon.ORCID 0000-0001-8666-3152
Andrea BolziccoPatients association 'Orchestra per la vita' Aps, Rome, Italy.ORCID 0009-0009-8955-9161
Vincenzo CerulloDrug Research Program, University of Helsinki, Helsinki, Finland.ORCID 0000-0003-4901-3796
Josephine K DermawanRobert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0002-1139-2914
Anna Maria FrezzaDepartment of Medical Oncology 2, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.ORCID 0000-0003-2335-7224
Antoine ItalianoEarly Phase Trials and Sarcoma Units, Institut Bergonie, Bordeaux, France.ORCID 0000-0002-8540-5351
Jia Xiang JinDivision of Translational Pediatric Sarcoma Research, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany.ORCID 0000-0001-6574-7816
Francois Le LoarerFaculty of Medicine, University of Bordeaux, Bordeaux, France.ORCID 0000-0001-8582-9819
Javier Martin-BrotoMedical Oncology Department, Fundación Jimenez Diaz University Hospital; University Hospital General de Villalba, and Instituto de Investigacion Sanitaria Fundacion Jimenez Diaz (IIS/FJD; UAM), Madrid, Spain.ORCID 0000-0001-7350-6916
Andrew PecoraJohn Theurer Cancer Center, Georgetown Lombardi Comprehensive Cancer Center, Washington, DC.ORCID 0009-0001-8034-932X
Antonio Perez-MartinezPatients association: 'MC4 in corsa per la vita!' ETS, Milan, Italy.ORCID 0000-0002-6436-9195
Yuen Bun TamDivision of Molecular Pathology, Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-1319-5148
Franck TirodeUniversité Claude Bernard, INSERM 1052, CNRS 5286, Cancer Research Center of Lyon, Centre Léon Bérard, Lyon, France.ORCID 0000-0003-4731-7817
Annalisa TramaDepartment of Epidemiology and Data Science; Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0001-8220-9833
Sandro PasqualiMolecular Pharmacology, Department of Experimental Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0003-4815-6293
Mariagrazia VesciaPatients association: 'MC4 in corsa per la vita!' ETS, Milan, Italy.ORCID 0009-0002-6984-8029
Lukas WortmannPatients association "Smarcb1" e.V., Bergisch Gladbach, Germany.ORCID 0009-0003-0717-8979
Michael WortmannPatients association "Smarcb1" e.V., Bergisch Gladbach, Germany.ORCID 0009-0006-3386-4333
Akihiko YoshidaDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-3373-0099
Kim WebbPatients association "Smarcb1" e.V., Bergisch Gladbach, Germany.ORCID 0009-0001-7011-2193
Paul H HuangDivision of Molecular Pathology, Institute of Cancer Research, London, United Kingdom.ORCID 0000-0003-3972-5087
Charles KellerChildren's Cancer Therapy Development Institute, Hillsboro, Oregon.ORCID 0000-0003-2505-7487
Cristina R AntonescuDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.ORCID 0000-0002-9717-8205

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Targeting Oncogenic Pathways in Genetically Complex SarcomasP50CA217694 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Marc Ladanyi · 2018 to 2026
$21.5M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA217694
6 · The paper itself

Abstract

Epithelioid sarcoma (EpS) is an ultra-rare malignant soft-tissue cancer mostly affecting adolescents and young adults. EpS often exhibits an unfavorable clinical course with fatal outcome in ∼50% of cases despite aggressive multimodal therapies combining surgery, chemotherapy, and irradiation. EpS is traditionally classified in a more common, less aggressive distal (classic) type and a rarer aggressive proximal type. Both subtypes are characterized by a loss of nuclear INI1 expression, most often following homozygous deletion of its encoding gene, SMARCB1-a core subunit of the SWI/SNF chromatin remodeling complex. In 2020, the EZH2 inhibitor tazemetostat was the first targeted therapy approved for EpS, raising new hopes. Still, the vast majority of patients did not benefit from this drug or relapsed rapidly. Further, other recent therapeutic modalities, including immunotherapy, are only effective in a fraction of patients. Thus, novel strategies, specifically targeted to EpS, are urgently needed. To accelerate translational research on EpS and eventually boost the discovery and development of new diagnostic tools and therapeutic options, a vibrant translational research community has formed in past years and held two international EpS digital expert meetings in 2021 and 2023. This review summarizes our current understanding of EpS from the translational research perspective and points to innovative research directions to address the most pressing questions in the field, as defined by expert consensus and patient advocacy groups.

Indexed as

SarcomaTranscription FactorsAdolescentChromosomal Proteins, Non-HistoneDNA-Binding ProteinsHomozygoteHumansSequence DeletionSMARCB1 ProteinYoung AdultChromosomal Proteins, Non-HistoneDNA-Binding ProteinsSMARCB1 ProteinTranscription Factors

Identifiers

PMID37916971
PMCPMC10947972

What OpenQuestion holds

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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.