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.
MAPPYACTS 2 is an ambispective (prospective and retrospective) international multicentric clinical study to provide clinical therapeutic recommendations, to set up the molecular and comprehensive clinical database of patients with relapsed or refractory pediatric malignancies in FMG2025 - Cancers et leucémies pédiatriques en échec de traitement or equivalent international projects, to collect the follow-up data on treatment and patients' outcome, in order to determine the outcome of the program in regard to benefit to the single patient, all the patients and to health care. It will also serve as a central link to interventional study platforms and international precision medicine programs, and cover and coordinate ancillary research studies that lead to improve treatment and outcome for children with advanced malignancies. Clinical recommendations and decisions following tumor sequencing are made based on discussions with biologists, scientists and physicians in the molecular and clinical molecular tumor boards run by the FMG2025 and MAPPYACTS 2 study teams. Associated ancillary research studies and links to clinical interventional studies are essential components of the program to perform clinical, translational and basic research in order to generate scientific knowledge and develop new treatment strategies that improve outcome of these patients. Research projects are discussed and agreed on in the MAPPYACTS 2 study committee.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
1,800
Biopsy and blood sample
CHU Amiens-Picardie
Amiens, France, France
RECRUITINGHopital Armand Trousseau
Paris, France, France
RECRUITINGCHU Saint Etienne
Saint-Etienne, France, France
RECRUITINGGustave Roussy
Paris, Villejuif, France
RECRUITINGCHU Angers
Angers, France
RECRUITINGCHU Besançon
Besançon, France
RECRUITINGCHU Pellegrin
Bordeaux, France
RECRUITINGCHRU Morvan
Brest, France
RECRUITINGCHU de Caen
Caen, France
RECRUITINGCHU Estaing
Clermont-Ferrand, France
RECRUITING...and 19 more locations
Overall survival (OS)
Defined as the time from study entry to death whatever the cause of death, after 3 years, for the whole cohort and according to cancer type.
Time frame: 3 years
The number of additional technologies and new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program.
The number of patients receiving matched targeted treatments The number of new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program The number of additional technologies that are introduced in the care for advanced pediatric cancers through this research program
Time frame: 3 years
The types of additional technologies and new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program.
The type of patients receiving matched targeted treatments The type of new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program The type of additional technologies that are introduced in the care for advanced pediatric cancers through this research program
Time frame: 3 years
Objective response rate on treatment attributed by the molecular tumor board in the clinical trial, overall and according to the treatment decision
Objective tumor response measured according to the standard for each tumor entity (i.e. RECIST 1.1, INRC, RANO, etc.). Assessed for the whole the prospective and retrospective cohorts, for each disease entity as well as for each suggested treatment and until last follow-up.
Time frame: 5 years
Progression-free survival (PFS)
Defined as the time interval from start of attributed treatment (targeted or not) to progression or death. They will be assessed for the whole the prospective and retrospective cohorts, for each disease entity as well as for each suggested treatment and until last follow-up.
Time frame: 5 years
5-year overall survival
Defined as the time from study entry to death whatever the cause of death, after 5 years. They will be assessed for the whole the prospective and retrospective cohorts,, for each disease entity as well as for each suggested treatment and until last follow-up.
Time frame: 5 years
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