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Pulmonary toxicity of craniospinal irradiation using helical tomotherapy

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dc.contributor.authorLee, Joongyo-
dc.contributor.authorKim, Euidam-
dc.contributor.authorKim, Nalee-
dc.contributor.authorSuh, Chang-Ok-
dc.contributor.authorChung, Yoonsun-
dc.contributor.authorYoon, Hong In-
dc.date.accessioned2022-07-06T10:14:08Z-
dc.date.available2022-07-06T10:14:08Z-
dc.date.created2022-04-06-
dc.date.issued2022-02-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/139485-
dc.description.abstractCraniospinal irradiation using helical tomotherapy (HT-CSI) has advantages in aspects of homogeneous dose distribution. Physicians, however, still have concerns of pulmonary toxicity due to HT-CSI's relatively large, low-dose irradiated volume from continuous and 360 degrees rotation delivery. In this study, we investigated the pulmonary toxicity of HT-CSI. We retrospectively reviewed 105 patients who received HT-CSI between January 2014 and December 2019. Grade 2 + pulmonary toxicities were evaluated. Intensive systemic treatment was defined as systemic treatment administration before, during, and after HT-CSI. V-X Gy was defined as % volume receiving >= X Gy. Thirteen patients (12.4%) presented with grade 2 + pulmonary toxicities after HT-CSI. Of these patients, only one experienced grade 2 radiation pneumonitis combined with pembrolizumab-induced pneumonitis. Conversely, pneumonia was observed in 12 patients. Intensive systemic treatment (p = 0.004), immunosuppressive drugs (p = 0.031), and bilateral lung V-5 Gy >= 65% (p = 0.031) were identified as independent risk factors for pneumonia. The risk factor for pneumonia in pediatric patients were immunosuppressive drugs (p = 0.035) and bilateral lung V-5 Gy >= 65% (p = 0.047). HT-CSI can be a safe treatment modality with tolerable pulmonary toxicities. Intensive systemic treatment, immunosuppressive drugs, and bilateral lung V-5 Gy >= 65% were significantly associated with pneumonia. In these patients, close follow-up should be considered for proper management of pneumonia.-
dc.language영어-
dc.language.isoen-
dc.publisherNATURE PORTFOLIO-
dc.titlePulmonary toxicity of craniospinal irradiation using helical tomotherapy-
dc.typeArticle-
dc.contributor.affiliatedAuthorChung, Yoonsun-
dc.identifier.doi10.1038/s41598-022-07224-1-
dc.identifier.scopusid2-s2.0-85125543757-
dc.identifier.wosid000761274300013-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.12, no.1, pp.1 - 9-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume12-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage9-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusPNEUMOCYSTIS-CARINII-PNEUMONIA-
dc.subject.keywordPlusRADIATION PNEUMONITIS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusRADIOTHERAPY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusTUMORS-
dc.subject.keywordPlusELECTRON-
dc.subject.keywordPlusRISK-
dc.identifier.urlhttps://www.nature.com/articles/s41598-022-07224-1-
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