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2023 GEIS Guidelines for gastrointestinal stromal tumors.
Serrano, César; Martín-Broto, Javier; Asencio-Pascual, José Manuel; López-Guerrero, José Antonio; Rubió-Casadevall, Jordi; Bagué, Silvia; García-Del-Muro, Xavier; Fernández-Hernández, Juan Ángel; Herrero, Luís; López-Pousa, Antonio; Poveda, Andrés; Martínez-Marín, Virginia.
Afiliación
  • Serrano C; Sarcoma Translational Research Group, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, Carrer de Natzaret, 115-117, Barcelona 08035, Spain.
  • Martín-Broto J; Medical Oncology Department, Fundación Jimenez Diaz University Hospital, Madrid, Spain.
  • Asencio-Pascual JM; University Hospital General de Villalba, Madrid, Spain Instituto de investigación Sanitaria Fundación Jimenez Diaz (IIS/FJD; UAM), Madrid, Spain.
  • López-Guerrero JA; Department of General Surgery, Gregorio Marañón University Hospital, Madrid, Spain.
  • Rubió-Casadevall J; Department of Surgery, Universidad Complutense de Madrid, Madrid, Spain.
  • Bagué S; Laboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
  • García-Del-Muro X; Department of Medical Oncology, Catalan Institute of Oncology, Girona Biomedical Research Institute (IDIBGI), Girona, Spain.
  • Fernández-Hernández JÁ; Department of Pathology, Santa Creu i Sant Pau University Hospital, Barcelona, Spain.
  • Herrero L; Department of Medical Oncology, Institut Català d'Oncologia, IDIBELL and University of Barcelona, Barcelona, Spain.
  • López-Pousa A; Department of Surgery, Virgen de la Arrixaca University Hospital, Murcia, Spain.
  • Poveda A; GIST advocacy group - Colectivo GIST, Valladolid, Spain.
  • Martínez-Marín V; Department of Pathology, Santa Creu i Sant Pau University Hospital, Barcelona, Spain.
Ther Adv Med Oncol ; 15: 17588359231192388, 2023.
Article en En | MEDLINE | ID: mdl-37655207
Gastrointestinal stromal tumor (GIST) is the most common malignant neoplasm of mesenchymal origin. GIST spans a wide clinical spectrum that ranges from tumors with essentially no metastatic potential to malignant and life-threatening spread diseases. Gain-of-function mutations in KIT or PDGFRA receptor tyrosine kinases are the crucial drivers of most GISTs, responsible for tumor initiation and evolution throughout the entire course of the disease. The introduction of tyrosine kinase inhibitors targeting these receptors has substantially improved the outcomes in this formerly chemoresistant cancer. As of today, five agents hold regulatory approval for the treatment of GIST: imatinib, sunitinib, regorafenib, ripretinib, and avapritinib. This, in turn, represents a success for a rare neoplasm. During the past two decades, GIST has become a paradigmatic model in cancer for multidisciplinary work, given the disease-specific particularities regarding tumor biology and tumor evolution. Herein, we review currently available evidence for the management of GIST. This clinical practice guideline has been developed by a multidisciplinary expert panel (oncologist, pathologist, surgeon, molecular biologist, radiologist, and representative of patients' advocacy groups) from the Spanish Group for Sarcoma Research, and it is conceived to provide, from a critical perspective, the standard approach for diagnosis, treatment, and follow-up.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Ther Adv Med Oncol Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Ther Adv Med Oncol Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido