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This is a clinical prospective, no-Profit, Interventional, Premarket Medical Device "early phase", multicentre, single-arm study, based on collecting data on predictive biomarkers of mCRC patients, integrate them with the results of the retrospective evaluation of outcomes and profiles of historical mCRC patients previously treated in the Oncology Units, in order to evaluate the efficacy of the best administered treatment. Results from the retrospective evaluation, will serve to build an AI-based profile capable to identify "good" or "poor" responders to therapy and to support the clinician towards the best treatment option. AI is a software based on algorithm defined as Medical Device Class IIa.
This is a clinical prospective, no-Profit, Interventional, Premarket Medical Device "early phase", multicentre, single-arm study, based on collecting data on predictive biomarkers of mCRC patients, integrate them with the results of the retrospective evaluation of outcomes and profiles of historical mCRC patients previously treated in the Oncology Units, in order to evaluate the efficacy of the best administered treatment. Results from the retrospective evaluation, will serve to build an AI-based profile capable to identify "good" or "poor" responders to therapy and to support the clinician towards the best treatment option. Following the first disease progression (PD), 2nd line therapy will be at Investigator's choice. The drugs under investigation are those commonly employed in mCRC patients as per usual standard of care. Artificial Intelligence (AI) is a software based on algorithm defined as Medical Device Class IIa. The REVERT clinical trial is study, inserted within a wider European Project. The clinical study will take advantage of the results of the retrospective evaluation of mCRC patients' outcomes and profiles, aimed at evaluate the efficacy of treatment strategies, that will performed during the early activities of the European Project. In such retrospective analysis AI and Machine Learning (ML) will be instructed and used to derive predictive clinical data, after having analysed all possible variables including known mutational, biochemical and clinical features of samples from mCRC patients historically treated in the Oncology Units participating to the project and stored in partner Biobanks. AI and ML methodologies are based on Support Vector Machines and combine Multiple Kernel Learning and Random Optimization, incorporating already available large databases with new, potential prognostic/predictive biomarkers (e.g., gene mutations, epigenetic changes, gene expression profiling signatures). The emerging results will be used to help the choice of the best combinatorial therapy, for every prospectively enrolled mCRC patient. Sex and gender differences, also according to sidedness, will be analysed to evaluate their impact on survival and quality of life (QoL) in patients with mCRC. Study length is planned to be about 24 months (12 months recruitment + 12 months of follow-up). The end of study is defined as the time when all enrolled patients will have experienced evidence of disease progression or will be out of treatment as per protocol, toxicity, medical decision or patient's withdrawal.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Scienze della Salute Università degli Studi di Firenze
Florence, Italy
Unità Oncologia Medica Dipartimento di Discipline Chirurgiche, Oncologiche e Stomatologiche
Palermo, Italy
Medical Oncology Unit, Department of Oncohematology, Policlinico Tor Vergata
Roma, Italy
"Grigore T. Popa" University of Medicine and Pharmacy of Iași
Iași, Iaşi, Romania
Regional Institute of Oncology
Iași, Iaşi, Romania
Hospital General Universitario Santa Lucía
Cartagena, Murcia, Spain
Start Date
March 21, 2023
Primary Completion Date
March 31, 2024
Completion Date
November 25, 2024
Last Updated
November 29, 2024
106
ACTUAL participants
AI
DEVICE
Lead Sponsor
University of Rome Tor Vergata
NCT07321106
NCT03694938
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06335147