MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
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 genomic alterations that could lead to an adapted targeted treatment. Furthermore, ancillary studies were associated exploring circulating tumor DNA, the immune contexture of tumors and developing Patient-Derived Xenografts (PDX). The FMG2025 project transfers the molecular profiling of advanced pediatric cancers into a global approach that is now considered standard of care in France. Subsequent clinical recommendations and decisions will be made based on discussions with biologists, scientist and physicians in the molecular and clinical molecular tumor boards. Associated ancillary research studies and links to clinical interventional studies remain essential elements of the program to provide clinical, translational and basic research in order to improve scientific knowledge. The program is articulated in two main parts that are closely interacting: FMG2025 - Cancers et leucémies pédiatriques en échec de traitement or equivalent international projects that cover the sequencing of tumor and blood samples and provide molecular reports. The clinical study MAPPYACTS 2 that provides clinical and therapeutic discussions of the sequencing results and therapy recommendations via the clinical molecular tumor board (CMTB) reports. It collects molecular and comprehensive clinical data of the patients registered in FMG2025 or equivalent international projects and thereby constitutes the critical link to clinical interventional studies and its sponsors ensuring facilitated access to these trials. It also covers and coordinates ancillary research studies. Due to the delay in opening of the MAPPYACTS 2 trial, clinical and molecular data for patients whose tumors were sequenced within FMG2025 or equivalent and not included in MAPPYACTS 2 before CMTB or equivalent, will be collected retrospectively after a specific patient/legal representative information and will contribute to the endpoints of the trial as adequate.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Dziecko lub młody dorosły (wiek ≤ 25 lat w momencie pierwszego rozpoznania) z potwierdzonym nowotworem litym lub białaczką, która wróciła lub nie reaguje na standardowe leczenie
- •Zakwalifikowany do badania FMG2025 i podpisana pisemna zgoda na udział w badaniu
- •Dostępna próbka guza (z biopsji, operacji lub archiwum z ostatnich 3 miesięcy)
- •Stan ogólny pacjenta pozwala na uczestnictwo w badaniu klinicznym (spodziewana długość życia > 3 miesiące)
- •Podpisana pisemna zgoda na MAPPYACTS 2 zgodnie z wymogami lokalnymi
- •Ubezpieczenie społeczne zgodnie z wymogami lokalnymi
✗ Disqualifies
- •Ciąża
- •Poważne problemy zdrowotne lub nieprawidłowości w badaniach laboratoryjnych, które mogą wpłynąć na wyniki badania
Simplified criteria — AI translation
Trial details
- Minimum age
- 6 Years
- Maximum age
- 25 Years
- Last updated (source)
- August 13, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (29)
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
CHU de Caen
Caen, France
CHU Estaing
Clermont-Ferrand, France
CHU Dijon François Mitterand
Dijon, France
CHU Grenoble Alpes
Grenoble, France
Centre Oscar Lambret
Lille, France
Chu Limoges
Limoges, France
IHOP
Lyon, France
CHU La Timone
Marseille, France
CHU Arnaud de Villeneuve
Montpellier, France
CHU Nantes
Nantes, France
CHU de Nice
Nice, France
Institut Curie
Paris, France
CHU Poitiers
Poitiers, France
CHU Reims- Hôpital Américain
Reims, France
CHU Rennes Hôpital Sud
Rennes, France
CHU de Rouen
Rouen, France
CHU de La Réunion site nord
Saint-Denis, France
Hôpital de Hautepierre
Strasbourg, France
Hôpital des Enfants - CHU de Toulouse
Toulouse, France
Hôpital Clocheville
Tours, France
CHRU Nancy Hôpital Enfants
Vandœuvre-lès-Nancy, France
Trial contact
Birgit GEOERGER, MD
Gwenaelle BOUDIER
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/14/2026.
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