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Molecular characteristics and therapeutic vulnerabilities across paediatric solid tumours.
Jones, David T W; Banito, Ana; Grünewald, Thomas G P; Haber, Michelle; Jäger, Natalie; Kool, Marcel; Milde, Till; Molenaar, Jan J; Nabbi, Arash; Pugh, Trevor J; Schleiermacher, Gudrun; Smith, Malcolm A; Westermann, Frank; Pfister, Stefan M.
Afiliación
  • Jones DTW; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Banito A; Pediatric Glioma Research Group, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Grünewald TGP; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Haber M; Pediatric Soft Tissue Sarcoma Research Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Jäger N; Max-Eder Research Group for Pediatric Sarcoma Biology, Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.
  • Kool M; German Cancer Consortium (DKTK), Partner Site Munich, Munich, Germany.
  • Milde T; Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Australia, Randwick, NSW, Australia.
  • Molenaar JJ; School of Women's & Children's Health, UNSW Australia, Randwick, NSW, Australia.
  • Nabbi A; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Pugh TJ; Division of Pediatric Neurooncology, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Schleiermacher G; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Smith MA; Division of Pediatric Neurooncology, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Westermann F; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Pfister SM; Clinical Cooperation Unit Pediatric Oncology, German Cancer Research Center (DKFZ) and German Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
Nat Rev Cancer ; 19(8): 420-438, 2019 08.
Article en En | MEDLINE | ID: mdl-31300807
ABSTRACT
The spectrum of tumours arising in childhood is fundamentally different from that seen in adults, and they are known to be divergent from adult malignancies in terms of cellular origins, epidemiology, genetic complexity, driver mutations and underlying mutational processes. Despite the immense knowledge generated through sequencing efforts and functional characterization of identified (epi-)genetic alterations over the past decade, the clinical implications of this knowledge have so far been limited. Novel preclinical platforms such as the European Innovative Therapies for Children with Cancer-Paediatric Preclinical Proof-of-Concept Platform and the US-based Pediatric Preclinical Testing Consortium are being developed to try to change this by aiming to recapitulate the extensive heterogeneity of paediatric tumours and thereby, hopefully, improve the ability to predict clinical benefit. Numerous studies have also been established worldwide to provide patients with access to real-time molecular profiling and the possibility of more precise mechanism-of-action-based treatments. In addition to tumour-intrinsic findings and mechanisms, ongoing studies are investigating features such as the immune microenvironment of paediatric tumours in comparison with adult cancers - currently of very timely clinical relevance. However, there is an ongoing need for rigorous preclinical biomarker and target validation to feed into the next generation of molecularly stratified clinical trials. This Review aims to provide a comprehensive state-of-the-art overview of the molecular landscape of paediatric solid tumours, including their underlying genomic alterations and interactions with the microenvironment, complemented with our current understanding of potential therapeutic vulnerabilities and how these can be preclinically tested using more accurate predictive methods. Finally, we provide an outlook on the challenges and opportunities associated with translating this overwhelming scientific progress into real clinical benefit.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pediatría / Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Nat Rev Cancer Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pediatría / Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Nat Rev Cancer Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article País de afiliación: Alemania