Evidence map›Paper›PMID 35292802›Full record

ArticleCancer discovery2022

The European MAPPYACTS Trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies.

Pablo Berlanga, Gaelle Pierron, Ludovic Lacroix, Mathieu Chicard, Tiphaine Adam de Beaumais, Antonin Marchais, Anne C Harttrampf, Yasmine Iddir, Alicia Larive, Aroa Soriano Fernandez and 19 more

2 registry-linked trialsAbstract readMulticenter Study
In one paragraph

Article in Cancer discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 100 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02613962 nacompletednot on this map

A Prospective, Multicentric Clinical Proof-of-concept Study to Stratify Targeted Therapies Adapted to Molecular Profiling of Relapsed or Refractory Pediatric Tumors

TypeinterventionalSponsorGustave Roussy, Cancer Campus, Grand ParisRan2016 to 2022Enrolled791ConditionsRelapsed or Refractory Pediatric TumorArmsbiopsy or surgical resection of tumor and blood sampling
NCT02813135 phase1 / phase2recruitingnot on this map

European Proof-of-Concept Therapeutic Stratification Trial of Molecular Anomalies in Relapsed or Refractory Tumors

TypeinterventionalSponsorGustave Roussy, Cancer Campus, Grand ParisRan2016 to 2031Enrolled472ConditionsPediatric CancerArmsRibociclib, Topotecan, Temozolomide, Everolimus, Adavosertib
3 · Its place in the literature

Who cites it

100 citing papers in PubMed, 1 synthesis or guideline pooled it.

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40 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors.

Pablo Berlanga *Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Gaelle Pierron *Unité de Génétique Somatique, Service de Génétique, Hospital Group, Institut Curie, Paris, France.ORCID 0000-0002-2536-7680
Ludovic Lacroix *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.ORCID 0000-0003-2535-1010
Mathieu ChicardINSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
Tiphaine Adam de BeaumaisClinical Research Direction, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Antonin MarchaisINSERM U1015, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Anne C HarttrampfDepartment of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Yasmine IddirINSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.ORCID 0000-0002-7022-0725
Alicia LariveBiostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
Aroa Soriano FernandezLaboratory of Translational Research in Child and Adolescent Cancer, Vall d'Hebron Research Institute (VHIR)-UAB, Barcelona, Spain.
Imene HezamDepartment of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Cecile ChevassusBiostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
Virginie BernardInstitut Curie Genomics of Excellence (ICGex) Platform, Research Center, Institut Curie, Paris, France.
Sophie CotteretDepartment of Pathology and Laboratory Medicine, Translational Research Laboratory and Biobank, AMMICA, INSERM US23/CNRS UMS3655, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Jean-Yves ScoazecDepartment of Pathology and Laboratory Medicine, Translational Research Laboratory and Biobank, AMMICA, INSERM US23/CNRS UMS3655, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.ORCID 0000-0003-1604-6823
Arnaud GauthierDepartment of Pathology, PSL Research University, Institut Curie, Paris, France.ORCID 0000-0003-3096-6204
Samuel AbbouDepartment of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.ORCID 0000-0002-7159-8869
Nadege CorradiniDepartment of Pediatric Oncology, Institut d'Hematologie et d'Oncologie Pédiatrique/Centre Léon Bérard, Lyon, France.
Nicolas AndréDepartment of Pediatric Hematology and Oncology, Hôpital de La Timone, AP-HM, Marseille, France.ORCID 0000-0002-6786-4968
Isabelle AertsSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), Institut Curie, PSL Research University, Paris, France.
Estelle ThebaudDepartment of Pediatric Oncology, Centre Hospitalier Universitaire, Nantes, France.
Michela CasanovaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
Cormac OwensPaediatric Haematology/Oncology, Children's Health Ireland, Crumlin, Dublin, Republic of Ireland.ORCID 0000-0001-6559-3239
Raquel Hladun-AlvaroDivision 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.
Stefan MichielsBiostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Saclay, Villejuif, France.
Olivier DelattreINSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
Gilles VassalClinical Research Direction, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Gudrun Schleiermacher *INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, PSL Research University, Institut Curie, Paris, France.
Birgit Geoerger *Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.ORCID 0000-0003-4361-3643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractMAPPYACTS (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.

Indexed as

CarcinomaCell-Free Nucleic AcidsAdaptive Clinical Trials as TopicAdolescentBiomarkers, TumorChildHigh-Throughput Nucleotide SequencingHumansMutationNeoplasm Recurrence, LocalPrecision MedicineProspective StudiesBiomarkers, TumorCell-Free Nucleic Acids

Identifiers

PMID35292802
PMCPMC9394403

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.