Profiling Advanced Solid Tumors and Blood Cancers
Using Molecular Testing to Match Patients with Targeted Early Phase Trials
Led by Institut Bergonié · Updated on 2025-10-02
10000
Participants Needed
7
Research Sites
91 weeks
Total Duration
AI-Summary
What this Trial Is About
This research aims to identify actionable molecular changes in patients with advanced solid tumors or blood cancers. It focuses on using next generation sequencing and immunological profiling to provide a detailed biological picture of each patients tumor. The goal is to help doctors personalize cancer treatments by matching tumor characteristics with targeted therapies in early phase clinical trials.
Participants will have new tumor biopsies and blood samples collected for genetic profiling. Frozen and paraffin embedded tumor materials, either from archival or new biopsies, will be used alongside four blood samples to assess molecular markers. Results from this profiling will be reviewed by a multidisciplinary tumor board to guide therapy decisions. Patients with identified molecular alterations may be offered participation in early phase clinical trials at Institut Bergoni or other French hospitals.
Throughout the study, researchers will monitor the proportion of patients with at least one genomic alteration within one month. They will also track how molecular profiling information is used for treatment decisions, safety of biopsy procedures, and screening failure rates. Patients will be followed until death or study completion. Participation may last several months with ongoing evaluation of molecular data and clinical outcomes.
CONDITIONS
Brief Title
Bergonie Institut Profiling : Fighting Cancer by Matching Molecular Alterations and Drugs in Early Phase Trials
Research Team
A
Antoine ITALIANO, MD, PhD
S
Simone MATHOULIN-PELISSIER, MD, PhD
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Diagnosis of solid malignant tumor or hematological malignancy
Social security coverage compliant with French biomedical research law
Signed and dated informed consent prior to study procedures
You will not qualify if you...
Individuals deprived of liberty or under guardianship
Pregnant or breastfeeding women
Previous enrollment in this study
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - Up to 1 month
Participants undergo tumor biopsy and blood sample collection for genetic profiling to identify molecular alterations.
1 to 2 visits depending on biopsy procedure
Long-term Monitoring
Duration - Up to 36 months
Participants with identified molecular alterations are monitored to assess the utilization of molecular profiling information and clinical outcomes until death or study termination.
Periodic visits depending on clinical follow-up
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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