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CompletedNCT04987476InnovRT-2Updated Nov 20, 2025

Rhabdoid Tumors Cellular Architecture by Single-cell Analyses (InnovRT-2)

An observational study in ATRT, sponsored by Assistance Publique - Hôpitaux de Paris. Completed at 1 site in France. Open to participants aged Up to 17 Years. Per ClinicalTrials.gov, last updated 2025-11-20.

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
15
Ages
Up to 17 Years
Sex
All
01

Study summary

The aim is to describe at the cellular level the heterogeneity of rhabdoid tumors, and identify how this diversity influences resistance to treatment.

Read the detailed description

Rhabdoid tumors are aggressive cancers of infancy. Although frequently chemosensitive at the very beginning, they very often show resistance, suggesting some intra-tumor diversity or plasticity. Moreover, morphological analysis of rhadoid tumors often reveal some variety in tumor cell shapes and immunohistochemical profiling. Altogether, this suggests some intra-tumor heterogeneity, that has been scarcely studied so far.

This project aims to describe the intra-tumor heterogeneity by single-cell sequencing approaches.

After surgical resection, fresh tumor samples will be dissected and analysed using the 10X Chromium technology. Briefly, cells will be grouped in clusters according to their gene expression signalling, and each cluster will be defined in comparison with all other ones. Differential analyses will allow identifying the main characteristic of each cell sub-population. Potential filiations between clusters will be analysed using classical algorithms. The study will be performed on 10 to 15 tumor samples.

02

Conditions studied

  • ATRT

Keywords

  • ATRT
  • SMARCB1
  • single-cell RNAseq
03

In context

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children having or likely having a rhabdoid tumor according to clinical and radiological features

Eligibility criteria

Inclusion Criteria:

  • Aged 0-17 years old
  • having a rhabdoid tumor according to clinical and radiological features Or likely having a rhabdoid tumor according to clinical and radiological features
  • surgical resection in standard care
  • sufficient material for both diagnosis and experimental procedures
  • parents' agreement
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
15 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • ATRT

    Children affected by an ATRT at time of surgical resection

    Biological: analyzes in singles cells

Interventions

  • Biologicalanalyzes in singles cells

    genome expression analyzes in single cells

06

What researchers measure

Primary outcomes

  1. Intra-tumor heterogeneity

    Identification of cell clusters - mean expression (RPKM unit) of gene set signtaures in each bioinformatically defined cluster

    Time frame: Inclusion

Secondary outcomes

  1. Cell clusters recurrent from one sample to the other

    Fraction/percentage of cell clusters defined by primary outcome that are specific to each tumor and those that are shared by several or all samples

    Time frame: Inclusion

  2. Naming of potential targetable gene

    Mean expression (RPKM unit) of targetable genes (defined by the existence of adequate pharmacological inhibitor) in each tumor sample and clusters

    Time frame: Inclusion

  3. Identification of cytotoxic cells

    Conducting therapeutic biological functional tests

    Time frame: Inclusion

07

Study locations

1 site
  • Institut Curie
    Paris, 75005, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04987476
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut Curie, URC-CIC Paris Descartes Necker Cochin
Responsible party
Sponsor
First posted
Aug 3, 2021
Start date
Mar 31, 2022
Primary completion
Feb 21, 2025
Completion
Feb 21, 2025
Last update
Nov 20, 2025

Study contacts

Kevin Beccaria, MD, PhD, Pr
study director · APHP Assistance Publique des Hôpitaux de Paris

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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