Publication:
Outcome of postoperative radiation therapy for pediatric intracranial ependymoma: a single-institution review

dc.contributor.authorRawee Ruangkanchanasetren_US
dc.contributor.authorThiti Swangsilpaen_US
dc.contributor.authorPutipun Puataweepongen_US
dc.contributor.authorMantana Dhanachaien_US
dc.contributor.authorAke Hansasutaen_US
dc.contributor.authorAtthaporn Boongirden_US
dc.contributor.authorNongnuch Sirachainanen_US
dc.contributor.authorSuradej Hongengen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.date.accessioned2020-01-27T09:37:01Z
dc.date.available2020-01-27T09:37:01Z
dc.date.issued2019-08-01en_US
dc.description.abstract© 2019, Springer-Verlag GmbH Germany, part of Springer Nature. Purpose: To report outcome of postoperative radiotherapy (RT) in both new and recurrent grade II and III intracranial ependymomas in children treated at Ramathibodi Hospital. Materials and methods: Between 2006 and 2017, 24 pediatric intracranial ependymomas treated with postoperative RT were retrospectively reviewed. The median age at diagnosis was 44.5 months (range, 4–165 months). There were 14 (58%) males. Fourteen (58%) patients had infratentorial tumor. The median maximal diameter of tumor at diagnosis was 4.45 cm (range, 2.2–10 cm). Fourteen (58%) patients had anaplastic tumor. Gross total resections were performed in 14 (58%) patients. The median prescribed dose was 54 Gy (range, 45–60 Gy). The median total treatment time was 43 days (range, 37–78 days). Results: The median clinical follow-up time was 44.5 months (range, 1–146 months). There were nine recurrences, five of which occurred at the primary tumor site. The estimated 5-year progression-free survival rate was 56%. The estimated 5-year overall survival rate was 75%. Extent of resection was the only factor associated with improved progression-free survival and overall survival after univariate testing. Six from nine patients with recurrent diseases underwent further surgery or further RT. These six patients had better median overall survival than the three who did not. Acute complication was mostly transient and tolerable. No late radiation effect was found. Conclusions: Postoperative radiation is an effective treatment. GTR is associated with better PFS and OS. Aggressive salvage local treatments for recurrent patients can result in good overall survival. Longer follow-up is needed in account for late relapse.en_US
dc.identifier.citationChild's Nervous System. Vol.35, No.8 (2019), 1313-1321en_US
dc.identifier.doi10.1007/s00381-019-04198-wen_US
dc.identifier.issn14330350en_US
dc.identifier.issn02567040en_US
dc.identifier.other2-s2.0-85067806586en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/51491
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067806586&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleOutcome of postoperative radiation therapy for pediatric intracranial ependymoma: a single-institution reviewen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067806586&origin=inwarden_US

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