RecruitingNot ApplicableNCT05691608

MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2


Sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Enrollment

1,800 participants

Start Date

Sep 9, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

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 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.


Eligibility

Min Age: 6 YearsMax Age: 25 Years

Inclusion Criteria7

  • Patient referred for sequencing of the tumor within the FMG2025 or equivalent program and written informed consent for FMG2025 "Cancers et leucémies pédiatriques en échec de traitement" or equivalent, according to local regulations
  • Written informed consent of MAPPYACTS 2 to collect molecular and comprehensive clinical data on cancer diagnosis, therapies, therapy outcomes, to provide clinical therapeutic recommendations, to collect follow-up data on treatment and patients' outcome; optional written consents to perform to ancillary research studies, according to local regulations. The written consent will include access to reimbursement data from the French national health insurance through linkage with the Système National des Données de Santé (SNDS) or equivalent.
  • Patient with histologically/cytologically 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
  • Planned tumor biopsy, surgical resection, bone marrow or blood sample or recently (preferably 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 expected to allow enrolment into an clinical trial
  • Patients affiliated with a Social Security Regimen or beneficiary of the same, as per local regulatory requirements

Exclusion Criteria2

  • 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

Interventions

BIOLOGICALSolid tumor and CT DNA

Biopsy and blood sample


Locations(29)

CHU La Timone

Marseille, France

Gustave Roussy

Paris, Villejuif, France

CHU Amiens-Picardie

Amiens, 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 Arnaud de Villeneuve

Montpellier, France

CHU Nantes

Nantes, France

CHU de Nice

Nice, France

Institut Curie

Paris, France

Hopital Armand Trousseau

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

CHU Saint Etienne

Saint-Etienne, 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

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NCT05691608


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