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dc.contributor.authorCorley, EA
dc.contributor.authorPace, E
dc.contributor.authorBarnacle, AM
dc.contributor.authorPatel, PA
dc.contributor.authorThway, K
dc.contributor.authorChisholm, JC
dc.coverage.spatialUnited States
dc.date.accessioned2023-02-14T13:48:14Z
dc.date.available2023-02-14T13:48:14Z
dc.date.issued2023-01-16
dc.identifier00043426-990000000-00171
dc.identifier.citationJournal of Pediatric Hematology/Oncology, 2023, Publish Ahead of Printen_US
dc.identifier.issn1077-4114
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5689
dc.identifier.eissn1536-3678
dc.identifier.eissn1536-3678
dc.identifier.doi10.1097/MPH.0000000000002612
dc.description.abstractAngiomatoid fibrous histiocytoma (AFH) is a soft tissue neoplasm of intermediate biological potential. Typically a slow-growing tumor, it can recur locally. Rarely, it manifests as a soft tissue sarcoma capable of metastasis. When metastases are nonamenable to local therapy, it is believed uniformly fatal. We present 3 patients with metastatic AFH who demonstrated a sustained response to chemotherapy; including one who achieved complete remission with cryoablation. These cases reinforce the potential value of chemotherapy in some patients with unresectable metastatic AFH and provide the first case in the literature of cryoablation in AFH.en_US
dc.formatPrint-Electronic
dc.languageeng
dc.language.isoengen_US
dc.publisherOvid Technologies (Wolters Kluwer Health)en_US
dc.relation.ispartofJournal of Pediatric Hematology/Oncology
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_US
dc.titleEvidence of Chemoresponsiveness in Unresectable Metastatic Angiomatoid Fibrous Histiocytoma.en_US
dc.typeJournal Article
dcterms.dateAccepted2022-11-13
dc.date.updated2023-02-13T22:30:56Z
rioxxterms.versionAMen_US
rioxxterms.versionofrecord10.1097/MPH.0000000000002612en_US
rioxxterms.licenseref.startdate2023-01-16
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36716049
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials in Children and Young People
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials in Children and Young People/Sarcoma Clinical Trials in Children and Young People (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people/Sarcoma Clinical Trials in Children and Young People (hon.)
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1097/mph.0000000000002612
pubs.volumePublish Ahead of Print
dc.contributor.icrauthorChisholm, Julia
icr.provenanceDeposited by Dr Julia Chisholm on 2023-02-13. Deposit type is initial. No. of files: 1. Files: JPHO-21-720_EC_answers[1].pdf
icr.provenanceDeposited by Mr Arek Surman (impersonating Dr Julia Chisholm) on 2023-02-14. Deposit type is subsequent. No. of files: 1. Files: JPHO-21-720_E.pdf


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