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The European MAPPYACTS Trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies.
Berlanga, Pablo; Pierron, Gaelle; Lacroix, Ludovic; Chicard, Mathieu; Adam de Beaumais, Tiphaine; Marchais, Antonin; Harttrampf, Anne C; Iddir, Yasmine; Larive, Alicia; Soriano Fernandez, Aroa; Hezam, Imene; Chevassus, Cecile; Bernard, Virginie; Cotteret, Sophie; Scoazec, Jean-Yves; Gauthier, Arnaud; Abbou, Samuel; Corradini, Nadege; André, Nicolas; Aerts, Isabelle; Thebaud, Estelle; Casanova, Michela; Owens, Cormac; Hladun-Alvaro, Raquel; Michiels, Stefan; Delattre, Olivier; Vassal, Gilles; Schleiermacher, Gudrun; Geoerger, Birgit.
Afiliación
  • Berlanga P; Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Pierron G; Unité de Génétique Somatique, Service de Génétique, Hospital Group, Institut Curie, Paris, France.
  • Lacroix L; Department of Pathology and Laboratory Medicine, Translational Research Laboratory and Biobank, AMMICA, INSERM US23/CNRS UMS3655, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Chicard M; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
  • Adam de Beaumais T; Clinical Research Direction, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Marchais A; INSERM U1015, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Harttrampf AC; Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Iddir Y; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
  • Larive A; Equipe SiRIC RTOP Recherche Translationelle en Oncologie Pédiatrique, Institut Curie, Paris, France.
  • Soriano Fernandez A; Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
  • Hezam I; Laboratory of Translational Research in Child and Adolescent Cancer, Vall d'Hebron Research Institute (VHIR)-UAB, Barcelona, Spain.
  • Chevassus C; Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Bernard V; Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
  • Cotteret S; Institut Curie Genomics of Excellence (ICGex) Platform, Research Center, Institut Curie, Paris, France.
  • Scoazec JY; Department of Pathology and Laboratory Medicine, Translational Research Laboratory and Biobank, AMMICA, INSERM US23/CNRS UMS3655, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Gauthier A; Department of Pathology and Laboratory Medicine, Translational Research Laboratory and Biobank, AMMICA, INSERM US23/CNRS UMS3655, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Abbou S; Department of Pathology, PSL Research University, Institut Curie, Paris, France.
  • Corradini N; Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • André N; Department of Pediatric Oncology, Institut d'Hematologie et d'Oncologie Pédiatrique/Centre Léon Bérard, Lyon, France.
  • Aerts I; Department of Pediatric Hematology and Oncology, Hôpital de La Timone, AP-HM, Marseille, France.
  • Thebaud E; UMR Inserm 1068, CNRS UMR 7258, Aix Marseille Université U105, Marseille Cancer Research Center (CRCM), Marseille, France.
  • Casanova M; SIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), Institut Curie, PSL Research University, Paris, France.
  • Owens C; Department of Pediatric Oncology, Centre Hospitalier Universitaire, Nantes, France.
  • Hladun-Alvaro R; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
  • Michiels S; Paediatric Haematology/Oncology, Children's Health Ireland, Crumlin, Dublin, Republic of Ireland.
  • Delattre O; Division of Paediatric Haematology and Oncology, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
  • Vassal G; Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
  • Schleiermacher G; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
  • Geoerger B; Institut Curie Genomics of Excellence (ICGex) Platform, Research Center, Institut Curie, Paris, France.
Cancer Discov ; 12(5): 1266-1281, 2022 05 02.
Article en En | MEDLINE | ID: mdl-35292802
ABSTRACT: MAPPYACTS (NCT02613962) is an international prospective precision medicine trial aiming to define tumor molecular profiles in pediatric patients with recurrent/refractory malignancies in order to suggest the most adapted salvage treatment. From February 2016 to July 2020, 787 patients were included in France, Italy, Ireland, and Spain. At least one genetic alteration leading to a targeted treatment suggestion was identified in 436 patients (69%) with successful sequencing; 10% of these alterations were considered "ready for routine use." Of 356 patients with follow-up beyond 12 months, 107 (30%) received one or more matched targeted therapies-56% of them within early clinical trials-mainly in the AcSé-ESMART platform trial (NCT02813135). Overall, matched treatment resulted in a 17% objective response rate, and of those patients with ready for routine use alterations, it was 38%. In patients with extracerebral tumors, 76% of actionable alterations detected in tumor tissue were also identified in circulating cell-free DNA (cfDNA). SIGNIFICANCE: MAPPYACTS underlines the feasibility of molecular profiling at cancer recurrence in children on a multicenter, international level and demonstrates benefit for patients with selected key drivers. The use of cfDNA deserves validation in prospective studies. Our study highlights the need for innovative therapeutic proof-of-concept trials that address the underlying cancer complexity. This article is highlighted in the In This Issue feature, p. 1171.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma / Ácidos Nucleicos Libres de Células Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Humans Idioma: En Revista: Cancer Discov Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma / Ácidos Nucleicos Libres de Células Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Humans Idioma: En Revista: Cancer Discov Año: 2022 Tipo del documento: Article País de afiliación: Francia