Clinical trial · Interventional
Improved Management of Soft Tissue Sarcomas Patients With an Optimized and Innovative Sorting Technology for Circulating Tumor Cells
NCT07401355CI-TRIAL-00102942LIGHT-CTCnot yet recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Diagnosis of Soft Tissue Sarcoma (STS) | Sarcoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Collection of tumor and blood sample | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- clinico-biological cohort
- description
- A clinico-biological cohort with collection of tumor and blood sample for detecting and sorting circulating tumor cells
- interventionNames
- Other: Collection of tumor and blood sample
Primary outcomes (1)
- measure
- 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
- timeFrame
- 48 months
- description
- Percentage of patients with detectable CTC
Secondary outcomes (5)
- measure
- Characterise the genetic profile of CTCs
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.