Actively Recruiting
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
Eligibility Criteria
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
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
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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