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

Status: Recruiting
Location: See all (21) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This trial is a translational, open-label, multi-sites, prospective and retrospective cohort study of 500 patients aimed at clinical and biological characterization of sarcoma of rare subtype. 400 patients will be included in this prospective cohort study; they will be identified in the investigating centers in the context of either routine care or a clinical study protocol. Retrospective cases of patients (100 cases in total) will be identified in all centers through the GSF/GETO clinical databases already setted up (including the clinical base Conticabase).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years at the time of study entry.

• Diagnosis of one of the following rare sarcoma subtype, confirmed by RRePS network:

‣ Clear Cell Sarcoma (CCS)

⁃ Epithelioid Sarcoma (ES)

⁃ Perivascular Epithelioid Cell neoplasm (PEComa)

⁃ Desmoplastic Small Round Cell Tumours (DSRCT)

⁃ Malignant Solitary Fibrous Tumours (mSFT)

⁃ Alveolar Soft Part Sarcoma (ASPS)

⁃ Epithelioid Hemangioendothelioma (EH)

⁃ Low-Grade Fibromyxoid Sarcoma (LGFS)

⁃ Sclerosing Epithelioid Fibrosarcoma (SEF).

• Localized/locally advanced or metastatic disease.

• In case of localized disease, treatment must not have been yet initiated before inclusion (except surgical excision).

• In case of metastatic disease, project of new line of systemic treatment must have been decided before inclusion.

• Patient followed in the center within a standard of care procedure or clinical trial.

• Archived tumor specimen at initial diagnosis available (before treatment initiation).

• Evaluable disease (measurable as per RECIST 1.1) or not.

• ECOG Performance status 0-3.

⁃ Patient able to participate and willing to give informed consent prior to performance of any study-related procedures.

⁃ Patient affiliated to a Social Health Insurance in France.

Locations
Other Locations
France
Chu Besancon - Site Jean Minjoz
RECRUITING
Besançon
Institut Bergonié
RECRUITING
Bordeaux
Institut Bergonié
RECRUITING
Bordeaux
Centre Jean Perrin
RECRUITING
Clermont-ferrand
Centre Georges François Leclerc
RECRUITING
Dijon
Centre Oscar Lambret
RECRUITING
Lille
Chu Dupuytren
RECRUITING
Limoges
Centre Leon Berard
RECRUITING
Lyon
Chu de Marseille - Hopital de La Timone
RECRUITING
Marseille
Institut Paoli-Calmettes
WITHDRAWN
Marseille
Centre Antoine Lacassagne
RECRUITING
Nice
Hôpital Cochin - Site Port-Royal
RECRUITING
Paris
Institut Curie
RECRUITING
Paris
Chu Poitiers
RECRUITING
Poitiers
Institut Godinot
RECRUITING
Reims
Centre Eugene Marquis
RECRUITING
Rennes
Institut de Cancerologie de L'Ouest - Site Rene Gauducheau
WITHDRAWN
Saint-herblain
Institut de Cancérologie Strasbourg Europe
RECRUITING
Strasbourg
Institut Universitaire du Cancer Toulouse - Oncopole
RECRUITING
Toulouse
Institut de Cancerologie de Lorraine
RECRUITING
Vandœuvre-lès-nancy
Institut Gustave Roussy
WITHDRAWN
Villejuif
Contact Information
Primary
Thibaud VALENTIN
Valentin.Thibaud@iuct-oncopole.fr
+33 (0)5 31 15 51 70
Backup
Frédéric CHIBON
frederic.chibon@inserm.fr
+33 (0)5 82 74 17 65
Time Frame
Start Date: 2021-04-26
Estimated Completion Date: 2031-04
Participants
Target number of participants: 400
Treatments
Other: Patient with Soft Tissue Sarcoma (Prospective cohort)
Sponsors
Leads: Institut Claudius Regaud

This content was sourced from clinicaltrials.gov