Collection of tumor and blood sample: Collection of tumor and blood sample for detecting and sorting circulating tumor cells
Study summary
This trial is a monocentric, clinico-biological cohort study with prospective enrollment, aiming to develop a method for detecting and sorting CTCs (circulating tumour cells) from liquid biopsies (fresh blood samples) in patients with advanced or metastatic soft tissue sarcomas.This study include collection of clinical data, of tumor samples (collected during standard of care).
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Male or female patients ≥ 18 years at the day of consenting;
* Histologically confirmed diagnosis of Soft Tissue Sarcoma (STS) excepted GIST.
* Metastatic disease or unresectable locally advanced malignancy for which standard therapy by anthracycline is decided;
* At least one measurable lesion as per RECIST version 1.1.;
* ECOG Performance Status of 0-2;
* Patients must have an adequate organ and bone marrow function at baseline;
* Patient should understand, sign, and date the written voluntary informed consent form prior to any protocol-specific procedures performed and should be able and willing to comply with procedures as per protocol;
* Covered by a medical insurance.
Exclusion Criteria:
* Evidence of significant uncontrolled concomitant disease that could affect compliance with the protocol or interpretation of results;
* Prior treatment with anthracycline;
* History of other malignancy other than study disease (except for basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix) unless the patient has been free of disease for at least 3 years;
* Metabolic syndrome;
* Pregnant or breast-feeding woman criteria
Primary outcome measure(s)
To develop a method for detecting and sorting CTCs (circulating tumour cells) from liquid biopsies (fresh blood samples) in patients with advanced or metastatic soft tissue sarcomas — 48 months Percentage of patients with detectable CTC
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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