Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID03967834

Multimodal Immune Characterization of Rare Soft Tissue Sarcoma - MIRAS Project from the French Sarcoma Group

Led by Institut Claudius Regaud · Updated on 2026-02-10

400

Participants Needed

20

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying rare subtypes of soft tissue sarcoma to better understand their clinical and biological characteristics. This is a translational, open-label study involving both prospective and retrospective cohorts, aiming to include 500 patients. The study includes patients with localized, locally advanced, or metastatic disease and seeks to evaluate outcomes such as metastasis-free survival and progression-free survival over 60 months. Patients will be enrolled from multiple centers, with 400 patients included prospectively during routine care or clinical studies, and 100 patients identified retrospectively from existing clinical databases. Tumor specimens and blood samples will be collected at diagnosis, after treatment completion or tumor evaluation, and at disease progression. Clinical and biological data will be gathered at baseline and regularly every 2 to 3 months for up to 5 years. Participants will undergo assessments including tumor specimen collection, blood sampling, and regular clinical evaluations to monitor disease progression and treatment effects. Researchers will measure survival outcomes and biological markers such as Cancer-Testis Antigens and the CINSARC signature. The study involves long-term follow-up of up to 60 months per patient to observe overall survival and other key outcomes.

CONDITIONS

Brief Title

Multimodal Immune Characterization of RAre Soft Tissue Sarcoma - MIRAS Project From SARRA (SARcome RAre) Project of the French Sarcoma Group

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older at study entry
  • Diagnosis of one of these rare sarcoma subtypes confirmed by RRePS network: Clear Cell Sarcoma, Epithelioid Sarcoma, Perivascular Epithelioid Cell neoplasm, Desmoplastic Small Round Cell Tumors, Malignant Solitary Fibrous Tumors, Alveolar Soft Part Sarcoma, Epithelioid Hemangioendothelioma, Low-Grade Fibromyxoid Sarcoma, or Sclerosing Epithelioid Fibrosarcoma
  • Localized, locally advanced, or metastatic disease
  • For localized disease, no treatment started before inclusion except surgical excision
  • For metastatic disease, new systemic treatment planned before inclusion
  • Patient followed under standard care or clinical trial
  • Archived tumor specimen available from initial diagnosis
  • Disease evaluable or measurable as per RECIST 1.1
  • ECOG Performance Status 0-3
  • Able and willing to give informed consent
  • Affiliated with Social Health Insurance in France
Not Eligible

You will not qualify if you...

  • Diagnosis of any other soft tissue sarcoma types
  • Conditions contraindicating study procedures
  • History of positive test for hepatitis B, hepatitis C, HIV, or AIDS
  • Psychological, familial, geographic, or social situations preventing consent or study compliance
  • Pregnant or breastfeeding women
  • Patients under guardianship or deprived of freedom by legal decision

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 5 years

Participants' tumor specimens and blood samples will be collected at diagnosis and at specific time points during the study. Clinical, biological, and disease data will be collected every 2 to 3 months for assessment of clinical benefit until disease progression or for up to 5 years.

Visits every 2 to 3 months until progression or for a maximum of 5 years

Trial Site Locations

Total: 20 locations

1

Chu Besancon - Site Jean Minjoz

Besançon, France, 25000

Actively Recruiting

2

Institut Bergonié

Bordeaux, France

Actively Recruiting

3

Centre Jean Perrin

Clermont-Ferrand, France, 63011

Actively Recruiting

4

Centre Georges François Leclerc

Dijon, France

Not Yet Recruiting

5

Centre Oscar Lambret

Lille, France, 59020

Actively Recruiting

6

Chu Dupuytren

Limoges, France

Actively Recruiting

7

Centre Leon Berard

Lyon, France, 69008

Actively Recruiting

8

Institut Paoli-Calmettes

Marseille, France, 13009

Withdrawn

9

Chu de Marseille - Hopital de La Timone

Marseille, France

Actively Recruiting

10

Centre Antoine Lacassagne

Nice, France, 06189

Actively Recruiting

11

Hôpital Cochin - Site Port-Royal

Paris, France

Actively Recruiting

12

Institut Curie

Paris, France

Actively Recruiting

13

Chu Poitiers

Poitiers, France

Actively Recruiting

14

Institut Godinot

Reims, France

Actively Recruiting

15

Centre Eugene Marquis

Rennes, France

Actively Recruiting

16

Institut de Cancerologie de L'Ouest - Site Rene Gauducheau

Saint-Herblain, France, 44805

Withdrawn

17

Hôpitaux Universitaires de Strasbourg

Strasbourg, France

Actively Recruiting

18

Institut Universitaire du Cancer Toulouse - Oncopole

Toulouse, France

Actively Recruiting

19

Institut de Cancerologie de Lorraine

Vandœuvre-lès-Nancy, France, 54519

Actively Recruiting

20

Institut Gustave Roussy

Villejuif, France, 94805

Withdrawn

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Research Team

T

Thibaud VALENTIN

F

Frédéric CHIBON

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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