2018
DOI: 10.21037/tgh.2018.07.09
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Current treatment strategies in pediatric gastrointestinal stromal cell tumor

Abstract: Gastrointestinal stromal tumors (GIST) are exceedingly rare tumors in the pediatric population. As a result, many clinicians either may never see this diagnosis or will encounter it only a few times throughout their careers. Additionally, the more we discover about this disease, it becomes evident that it represents a distinct clinical entity from adult GIST. Many of the treatments and strategies used to combat the adult tumor are either ineffective or may be harmful to the pediatric population with this disea… Show more

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Cited by 10 publications
(5 citation statements)
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References 42 publications
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“…All tumours of mesenchymal origin that express the membrane protein kit (CD117) or which have a mutation in platelet-derived-growth factor a (PDGFRA) should be considered as GISTs [ 3 – 6 ].…”
Section: Epidemiology Biology and Clinical Aspectsmentioning
confidence: 99%
“…All tumours of mesenchymal origin that express the membrane protein kit (CD117) or which have a mutation in platelet-derived-growth factor a (PDGFRA) should be considered as GISTs [ 3 – 6 ].…”
Section: Epidemiology Biology and Clinical Aspectsmentioning
confidence: 99%
“…Due to the complexity of the mutations involved in pediatric GIST and its consequences in therapeutic management, the importance of referral to specialized centers should be emphasized when determining adjuvant therapies for the pediatric patient presenting with GIST. [15] Taking into account all of the above, we can conclude that pediatric GISTs are extremely rare, therefore, diagnoses are usually made with delays. GISTs should be considered as a differential diagnosis in patients with anemia and gastrointestinal bleeding.…”
Section: Discussionmentioning
confidence: 99%
“…It also allows for the classification of GIST: some children have an adult-type tumor that possesses KIT or PDGFRA mutations, which may allow for the use of imatinib (especially exon 9 or 11 KIT mutations that are sensitive to imatinib treatment) [ 8 ]. Pediatric-type GIST may be treated with different agents compatible with the exact genetic alterations [ 9 , 10 ].…”
Section: Introductionmentioning
confidence: 99%