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Record W4416087792 · doi:10.1093/neuped/wuaf013

Epithelioid sarcoma in patients with rhabdoid tumor predisposition syndrome (RTPS): A novel cancer in the RTPS spectrum

2025· article· en· W4416087792 on OpenAlexaff
Meziane Brizini, Nikhil Raghuram, Stacy Chapman, Anna C. Shawyer, Suyin A. Lum Min, Clyde H. Wilkes, Sate Hamza, Paul C. Nathan, Hanning Chen, Annie Huang, Lucie Lafay‐Cousin, Magimairajan Vanan

Bibliographic record

VenueNeuro-Oncology Pediatrics · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicChromatin Remodeling and Cancer
Canadian institutionsAlberta Children's HospitalUniversity of CalgaryHospital for Sick ChildrenUniversity of ManitobaManitoba HealthResearch Institute in Oncology and HematologyManitoba Beekeepers' AssociationChildren's Hospital Research Institute of ManitobaCancerCare ManitobaResearch Manitoba
Fundersnot available
KeywordsSMARCB1Epithelioid sarcomaAtypical teratoid rhabdoid tumorMalignancyCancerSarcomaSoft tissue sarcomaSurgical oncology

Abstract

fetched live from OpenAlex

Abstract Background Rhabdoid tumor predisposition syndrome (RTPS) is characterized by germline biallelic loss of SMARCB1 (RTPS1) or SMARCA4 genes, leading to early-onset tumors primarily in the brain and kidneys. Epithelioid sarcoma (EpS) is a rare malignant soft tissue sarcoma in children and young adults, characterized by loss of nuclear SMARCB1 expression. Here, we describe survivors of atypical teratoid rhabdoid tumors (ATRT) with RTPS1 who developed EpS during follow-up. Methods Data were collected through a retrospective chart review of 4 patients with RTPS and ATRT diagnosed with EpS during routine follow-up. A literature review on RTPS and EpS was also conducted. Results All 4 patients were diagnosed with ATRT and RTPS1 in infancy and treated with surgery, high-dose chemotherapy, and autologous stem cell transplantation. Relapse occurred in 3 of the 4 patients, with 2 patients undergoing surgery followed by focal radiation. EpS was diagnosed at regular follow-up, with patients presenting with multiple skin lesions in their extremities (hands, fingers). Histopathological analysis confirmed EpS with characteristic loss of SMARCB1 expression. Staging scans showed no evidence of disseminated disease. All 4 patients underwent surgical excision with negative margins, and 2 patients experienced multiple local recurrences managed with wide surgical excision. A literature review identified 1 additional case of RTPS1 with metachronous ATRT and late-onset EpS. Conclusions Our findings, supported by literature review, suggest that EpS is a primary malignancy within the RTPS1 cancer spectrum. Recognizing this predisposition is critical for implementing appropriate long-term surveillance and early intervention strategies in patients with RTPS1.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.023
Threshold uncertainty score0.645

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.004
GPT teacher head0.240
Teacher spread0.236 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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