Targeted treatment of refractory primitive neuroectodermal tumor arising from an immature teratoma with crizotinib leading to a sustained response

dc.contributor.authorSnyder, Benjamin M.
dc.contributor.authorLion, Alex H.
dc.contributor.authorHelvie, Amy E.
dc.contributor.authorMarshall, Mark S.
dc.contributor.authorFerguson, Michael J.
dc.contributor.departmentPediatrics, School of Medicine
dc.date.accessioned2023-10-18T12:51:36Z
dc.date.available2023-10-18T12:51:36Z
dc.date.issued2023-01-03
dc.description.abstractHere we present a case of metastatic PNET which arose from an immature teratoma that was refractory to standard Ewing sarcoma chemotherapy. This PNET was determined to have elevated levels of ALK protein via IHC. The patient was treated with crizotinib on a palliative basis with a sustained response.
dc.eprint.versionFinal published version
dc.identifier.citationSnyder BM, Lion AH, Helvie AE, Marshall MS, Ferguson MJ. Targeted treatment of refractory primitive neuroectodermal tumor arising from an immature teratoma with crizotinib leading to a sustained response. Clin Case Rep. 2023;11(1):e6779. Published 2023 Jan 3. doi:10.1002/ccr3.6779
dc.identifier.urihttps://hdl.handle.net/1805/36432
dc.language.isoen_US
dc.publisherWiley
dc.relation.isversionof10.1002/ccr3.6779
dc.relation.journalClinical Case Reports
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectEwing sarcoma
dc.subjectPNET
dc.subjectCrizotinib
dc.subjectPrecision oncology
dc.titleTargeted treatment of refractory primitive neuroectodermal tumor arising from an immature teratoma with crizotinib leading to a sustained response
dc.typeArticle
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