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Gastrointestinal stromal tumours (GISTs) are malignant mesenchymal tumours with a variable clinical behaviour, marked by differentiation towards the interstitial cells of Cajal.1 GISTs belong to the family of soft tissue sarcomas (STSs) but are treated separately due to their peculiar histogenesis, clinical behaviour and specific therapy. This European Society for Medical Oncology (ESMO)–European Reference Network for Rare Adult Solid Cancers (EURACAN)–European Reference Network for Genetic Tumour Risk Syndromes (GENTURIS) Clinical Practice Guideline (CPG) will cover GISTs while other STSs are covered in the ESMO–EURACAN–European Reference Network for Paediatric Oncology (ERN PaedCan)–GENTURIS STS CPG.
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Gastrointestinal stromal tumour, Gastrointestinal Stromal Tumors, Medizin, Tyrosine kinase inhibitor, Sarcoma, gastrointestinal stromal tumour, GIST; clinical practice guidelines; gastrointestinal stromal tumour; surgery; tyrosine kinase inhibitor, surgery, tyrosine kinase inhibitor, Humans, Surgery, Clinical practice guidelines, clinical practice guidelines, clinical practice guidelines; gastrointestinal stromal tumour; GIST; surgery; tyrosine kinase inhibitor, GIST, Follow-Up Studies, Gastrointestinal Neoplasms
Gastrointestinal stromal tumour, Gastrointestinal Stromal Tumors, Medizin, Tyrosine kinase inhibitor, Sarcoma, gastrointestinal stromal tumour, GIST; clinical practice guidelines; gastrointestinal stromal tumour; surgery; tyrosine kinase inhibitor, surgery, tyrosine kinase inhibitor, Humans, Surgery, Clinical practice guidelines, clinical practice guidelines, clinical practice guidelines; gastrointestinal stromal tumour; GIST; surgery; tyrosine kinase inhibitor, GIST, Follow-Up Studies, Gastrointestinal Neoplasms
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