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MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2

RecruitingNAAges 6 Years - 25 YearsAllGustave Roussy, Cancer Campus, Grand Paris
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In plain words

What the trial is, and whether it could suit you

FMG2025 continues the previous efforts to propose treatment for patients based on the molecular characteristics of their tumor at treatment failure in cancer precision medicine trials within standard of care in France. However, whereas FMG2025 is a descriptive effort providing the basis for clinical decisions, MAPPYACTS 2 will translate these findings to clinical actions. The symbiosis is critical to advance patient care. Since 2012, the molecular profiling trials "MOlecular Screening for CAncer Treatment Optimization" (MOSCATO-01) and "MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification" (MAPPYACTS) have included pediatric and adolescent patients with recurrent or refractory malignancy that underwent on-purpose biopsy or surgical intervention. Whole Exome Sequencing of tumor and normal tissue and RNA Sequencing of tumor tissue have been applied to detect g

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patient referred for sequencing of the tumor within the FMG2025 or equivalent program and written consent for FMG2025 - Cancers et leucémies pédiatriques en échec de traitement or equivalent signed * Written informed consent for MAPPYACTS 2 (or non-opposition for retrospective clinical data collection) according to local or national regulations * Patient with confirmed solid tumor or leukemia which is relapsed or refractory to standard treatment and who is potentially eligible for an experimental treatment or an early phase clinical trial at the time of tumor sequencing * Planned tumor biopsy, surgical resection, bone marrow or blood sample or recently (possibly within the last 3 months) archived frozen tumor material available of the current recurrent or refractory disease * Patients aged ≤ 25 years at the time of initial diagnosis * Performance status and life expectancy \> 3 months at the time of tumor sequencing that allows enrolment into an experimental trial * Patients affiliated with a Social Security Regimen or beneficiary of the same as per local regulatory requirements Exclusion Criteria: * Any concurrent illness or laboratory abnormality that, in the opinion of the investigator, is likely to interfere with the interpretation of study results * Pregnant women
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What it tests

  • Solid tumor and CT DNA
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Where

29 sites
CHU Amiens-Picardie
Amiens, France
Hopital Armand Trousseau
Paris, France
CHU Saint Etienne
Saint-Etienne, France
Gustave Roussy
Paris, France
CHU Angers
Angers, France
CHU Besançon
Besançon, France
CHU Pellegrin
Bordeaux, France
CHRU Morvan
Brest, France

…and 21 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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