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).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
400
* Tumor specimens will be collected for the study at diagnosis. * A blood sample will be collected in all included patients at baseline, after the completion of the treatment (for patients included with a localized disease) or at the time of the first tumoral evaluation (for patients included with a metastatic disease), and at the time of progression. * Patient's data (clinical, biological and disease data) will also be collected at baseline visit and then at each time point planned in the center for clinical benefit assessment (i.e. every 2 or 3 months) until progression or for a maximum duration of 5 years.
Chu Besancon - Site Jean Minjoz
Besançon, France
RECRUITINGInstitut Bergonié
Bordeaux, France
RECRUITINGCentre Jean Perrin
Clermont-Ferrand, France
RECRUITINGCentre Georges François Leclerc
Dijon, France
NOT_YET_RECRUITINGCentre Oscar Lambret
Lille, France
RECRUITINGChu Dupuytren
Limoges, France
RECRUITINGCentre Leon Berard
Lyon, France
RECRUITINGInstitut Paoli-Calmettes
Marseille, France
WITHDRAWNChu de Marseille - Hopital de La Timone
Marseille, France
RECRUITINGCentre Antoine Lacassagne
Nice, France
RECRUITING...and 10 more locations
Metastasis-free survival for patients with localized disease.
Time frame: 60 months for each patients
Progression-free survival for patients with metastatic disease.
Time frame: 60 months for each patients
Cancer-Testis Antigens (CTA) expression.
Time frame: 60 months for each patients
The rate of patients presenting high-risk CINSARC (Complexity Index in SARComas) signature.
Time frame: 60 months for each patients
Overall survival.
Time frame: 60 months for each patients
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