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Risk stratification of symptomatic brain metastases by clinical and FDG PET parameters for selective use of prophylactic cranial irradiation in patients with extensive disease of small cell lung cancer

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dc.contributor.authorChung, Joo-Hyun-
dc.contributor.authorKang, Seo Young-
dc.contributor.authorWu, Hong-Gyun-
dc.contributor.authorSeo, Young Seok-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorKang, Keon Wook-
dc.contributor.authorKim, Hak Jae-
dc.contributor.authorCheon, Gi Jeong-
dc.date.accessioned2021-01-31T08:07:34Z-
dc.date.available2021-01-31T08:07:34Z-
dc.date.created2020-05-14-
dc.date.created2020-05-14-
dc.date.created2020-05-14-
dc.date.issued2020-02-
dc.identifier.citationRadiotherapy and Oncology, Vol.143, pp.81-87-
dc.identifier.issn0167-8140-
dc.identifier.other99612-
dc.identifier.urihttps://hdl.handle.net/10371/171829-
dc.description.abstractPurpose: To identify risk factors for developing symptomatic brain metastases and evaluate the impact of prophylactic cranial irradiation (PCI) on brain metastasis-free survival (BMFS) and overall survival (OS) in extensive disease small cell lung cancer (ED-SCLC). Materials and methods: Among 190 patients diagnosed with ED-SCLC who underwent FDG PET/CT and brain Magnetic Resonance Imaging (MRI) prior to treatment, 53 (27.9%) received PCI while 137 (72.1%) did not. Prognostic index predicting a high risk of symptomatic brain metastases was calculated for the group without receiving PCI (observation group, n = 137) with Cox regression model. Results: Median follow-up time was 10.6 months. Multivariate Cox regression showed that the following three factors were associated with a high risk of symptomatic brain metastases: the presence of extrathoracic metastases (p = 0.004), hypermetabolism of bone marrow or spleen on FDG PET (p < 0.001), and high neutrophil-to-lymphocyte ratio (p = 0.018). PCI significantly improved BMFS in high-risk patients (1-year rate: 94.7% vs. 62.1%, p = 0.001), but not in low-risk patients (1-year rate: 100.0% vs. 87.7%, p = 0.943). However, PCI did not improve OS in patients at high risk for symptomatic brain metastases (1-year rate: 65.2% vs. 50.0%, p = 0.123). Conclusion: Three prognostic factors (the presence of extrathoracic metastases, hypermetabolism of bone marrow or spleen on FDG PET, and high neutrophil-to-lymphocyte ratio) were associated with a high risk of symptomatic brain metastases in ED-SCLC. PCI was beneficial for patients at a high risk of symptomatic brain metastases in terms of BMFS, but not OS. Thus, selective use of PCI in ED-SCLC according to the risk stratification is recommended. (C) 2020 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleRisk stratification of symptomatic brain metastases by clinical and FDG PET parameters for selective use of prophylactic cranial irradiation in patients with extensive disease of small cell lung cancer-
dc.typeArticle-
dc.contributor.AlternativeAuthor천기정-
dc.contributor.AlternativeAuthor김동완-
dc.contributor.AlternativeAuthor김학재-
dc.contributor.AlternativeAuthor강건욱-
dc.contributor.AlternativeAuthor우홍균-
dc.identifier.doi10.1016/j.radonc.2020.01.009-
dc.citation.journaltitleRadiotherapy and Oncology-
dc.identifier.wosid000519526300012-
dc.identifier.scopusid2-s2.0-85079068036-
dc.citation.endpage87-
dc.citation.startpage81-
dc.citation.volume143-
dc.identifier.sci000519526300012-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorWu, Hong-Gyun-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.contributor.affiliatedAuthorKang, Keon Wook-
dc.contributor.affiliatedAuthorKim, Hak Jae-
dc.contributor.affiliatedAuthorCheon, Gi Jeong-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTO-LYMPHOCYTE RATIO-
dc.subject.keywordPlusBONE-MARROW-
dc.subject.keywordPlusEMISSION-TOMOGRAPHY-
dc.subject.keywordPlusF-18-FDG UPTAKE-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusIMPROVES-
dc.subject.keywordAuthor[F-18]FDG PET-
dc.subject.keywordAuthorED-SCLC-
dc.subject.keywordAuthorSymptomatic brain metastases-
dc.subject.keywordAuthorProphylactic cranial irradiation-
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