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Spots Global Cancer Trial Database for A Master Protocol Empowering Mechanobiology Translation Research in Breast Cancer

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Trial Identification

Brief Title: A Master Protocol Empowering Mechanobiology Translation Research in Breast Cancer

Official Title: A Master Protocol Empowering Mechanobiology Translation Research in Breast Cancer

Study ID: NCT04625023

Conditions

Breast Cancer

Interventions

Observational

Study Description

Brief Summary: METAMECH is a master observational protocol designed to empower a bi-directional collaboration between basic and clinical research, an essential prerequisite to feed and implement precision oncology. METAMECH will follow a stage-mixed cohort of at least 500 patients through their course of treatments, until death or a minimum of 5 years. Patients will be longitudinally sampled and matched clinical data (including imaging) will be collected. Via a multi-tiered informed consensus process, METAMECH will also allow to develop companion diagnostics for molecular enrichment strategies in AIRC-driven proof-of-concept trials.

Detailed Description: METAMECH has been designed to streamline the study of the co-evolutionary landscape between tumor and host cells in a cohort of breast cancer (BC) patients, with the aim of understanding how their outcomes can be significantly improved (e.g. reduction of their chance of recurrence and survival improve). This clinical resource for integrative clinical data and sample collection will allow to generate hypotheses on mechanisms supporting the outgrowth of human metastases, mine for new potentially actionable targets and the selection of appropriate patients for experimentally-driven trials. To achieve the required level of 'experimental precision', patients will enter METAMECH at two different 'therapeutic checkpoints': i) prior to a tumor sampling event (surgery, biopsy) or ii) prior to any line of treatment. To optimize the enrollment of patients, the longitudinal collection of data/samples and their logistic management, METAMECH has been designed as a flexible infrastructure organized in Tiers for the stepwise comprehension of the biological processes that drive tumor evolution, and precisely: * TIER0, Retrieving: the ability to retrospectively retrieve clinically annotated BC archival samples to validate/discover new mechanotransduction-linked biomarkers; * TIER1, Recording: the ability to prospectively record BC characteristics under standard of care treatments and to define new mechanotransduction-linked biomarkers; * TIER2, Modelling: the ability to develop pertinent experimental models to study the aberrant mechanisms underlying the metastatic outgrowth and define mechanotransduction-targeting therapeutic strategies; * TIER3, Linking: the ability to access data and samples of patients enrolled in POC trials to prove the efficacy and study/understand resistance mechanisms of mechanotransduction-targeting therapies.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Asst Papa Giovanni Xxiii, Bergamo, , Italy

Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, , Italy

Fondazione IRCCS, Istituto Neurologico Carlo Besta, Milan, , Italy

Azienda Ospedaliero Universitaria Maggiore della Carità di Novara, Novara, , Italy

Istituto Oncologico Veneto IRCCS (IOV), Padova, , Italy

Fondazione IRCCS, Policlinico San Matteo Pavia, Pavia, , Italy

Istituto Nazionale Tumori Regina Elena di Roma - Istituti Fisioterapici Ospitalieri (IFO), Roma, , Italy

Contact Details

Name: Silvia Marsoni, MD

Affiliation: IFOM- FIRC Institute of Molecular Biology

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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