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MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2

MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05691608
Acronym
MAPPYACTS2
Enrollment
1800
Registered
2023-01-20
Start date
2022-09-09
Completion date
2030-09-09
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Solid Tumor

Brief 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 (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.

Detailed description

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.

Interventions

BIOLOGICALSolid tumor and CT DNA

Biopsy and blood sample

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 25 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS)3 yearsDefined 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.
The number of additional technologies and new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program.3 yearsThe 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
The types of additional technologies and new treatment strategies that are introduced in the care for advanced pediatric cancers through this research program.3 yearsThe 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

Secondary

MeasureTime frameDescription
Objective response rate on treatment attributed by the molecular tumor board in the clinical trial, overall and according to the treatment decision5 yearsObjective 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.
Progression-free survival (PFS)5 yearsDefined 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.
5-year overall survival5 yearsDefined 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.

Countries

France

Contacts

CONTACTBirgit GEOERGER, MD
Birgit.GEOERGER@gustaveroussy.fr+33 (0)1 42 11 46 61
CONTACTGwenaelle BOUDIER
gwenaelle.boudier@gustaveroussy.fr+33 (0)1 42 11 58 38
PRINCIPAL_INVESTIGATORBirgit GEOERGER, MD

Gustave Roussy, Cancer Campus, Grand Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026