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CancerIndex

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Childhood Rhabdomyosarcoma · CancerIndex

Cancers
Neoplasm
Neoplasm by Special Category
Malignant Neoplasm
Sarcoma
Soft Tissue Sarcoma
Childhood Soft Tissue Sarcoma
Childhood Rhabdomyosarcoma

Subtype

Childhood Rhabdomyosarcoma

CI-CAN-00004908Explore in graph →

Pediatric6 active trials

NCIt: C7705

Overview
Statistics
Survival
Genomics
Variants & evidence
Drugs
Trials38
Research
Rankings
Sources & provenance

Data completeness2 / 7 dimensions

Epidemiology (no data yet)
Survival (no data yet)
Trials (data present)
Literature (data present)
Genomics (no data yet)
Evidence (no data yet)
Therapies (no data yet)

Computed from entity_counters.completeness · refreshed after each connector run

Definition

What this entity is

An aggressive malignant mesenchymal neoplasm arising from skeletal muscle in children. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomic sites.

Definition text as published by ncit-evsProvenance

Source: NCI Thesaurus (NCIt)
Dataset: NCI Thesaurus
Version: 26.08e
Retrieved: Sep 8, 2026
Layer: raw (as published)
Evidence: expert curation
License: CC BY 4.0
Run: ING-NCITEVS-20260908-000001

Open at source Curated

Data updated 22 days agoSource updated 26.08e

Taxonomy

Position in the hierarchies

Several hierarchies coexist; edges are listed per hierarchy type with their source.

Parents

ncit

Childhood Soft Tissue SarcomaSubtype
RhabdomyosarcomaSubtype

Children (5)

ncit

Childhood Alveolar Rhabdomyosarcoma
Childhood Embryonal Rhabdomyosarcoma1 sub
Childhood Pleomorphic Rhabdomyosarcoma
Childhood Rhabdomyosarcoma with Mixed Embryonal and Alveolar Features
Childhood Spindle Cell Rhabdomyosarcoma

8 descendants in total; counters on this page aggregate over all of them.

Anatomy

Anatomical sites

Connective and Soft TissueC3810

Record

Identity

CancerIndex ID: CI-CAN-00004908
Entity type: Subtype
Malignant: Yes
Solid / hematologic: Solid tumor
Pediatric relevant: Yes
Rare cancer: Unknown (no incidence data yet)
Hierarchy depth: 6
Classification version: 26.08e
Semantic types: Neoplastic Process
Status: Active
Record updated: 2026-09-08

Coverage

Data completeness

Trials (all / active): 38 / 6

Publications (all / 5y)

14,019 / 2,853

Evidence items

0

Genes / variants

0 / 0

Drugs (any / approved)

0 / 0

Genomic cohorts

0

Epidemiology / survival obs.

0 / 0

Data updated 18 hours agoSource updated unknowncounters aggregate over descendants

Names

Synonyms (3)

Pediatric Rhabdomyosarcomasynonym · NCIt
Rhabdomyosarcomasynonym · NCIt
Rhabdomyosarcoma pediatricsynonym · NCIt

CancerIndex is a research and information platform. It does not diagnose and does not recommend treatment.

Key figures

At a glance

Each figure carries its unit, period and source; ranks link to "Why this rank?".

No registry-level ancestor: burden figures are published for the mutually exclusive top-level site groups only, and this entity does not descend from one. Global figures (IARC / GLOBOCAN) stay under license review and SEER awaits credentials.

Active trials6countcurrent registry status · entity + descendantsclinicaltrialsComputedrank #703 of 1,654 (World · both sexes · all ages · latest · all malignant entities)
Recruiting trials2countstatus RECRUITING · entity + descendantsclinicaltrialsComputedrank #743 of 1,277 (World · both sexes · all ages · latest · all malignant entities)
Curated evidence items0countaccepted CIViC items · entity + descendantscivicComputednot in a current ranking snapshot
Publications, last 12 months545countPubMed records · stored query · 12-month windowpubmedComputedrank #140 of 2,294 (World · both sexes · all ages · latest · all malignant entities)
Genomic cohorts0countopen GDC projects · entity + descendantsgdcComputednot in a current ranking snapshot

Data updated 18 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants