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Clinical Course of Neuroendocrine Tumors With Different Origins (the Pancreas, Gastrointestinal Tract, and Lung)
DC Field | Value | Language |
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dc.contributor.author | Kim, Su-Jung | - |
dc.contributor.author | Kim, Jin Won | - |
dc.contributor.author | Oh, Do-Youn | - |
dc.contributor.author | Han, Sae-Won | - |
dc.contributor.author | Lee, Se-Hoon | - |
dc.contributor.author | Kim, Dong-Wan | - |
dc.contributor.author | Im, Seock-Ah | - |
dc.contributor.author | Kim, Tae-You | - |
dc.contributor.author | Heo, Dae Seog | - |
dc.contributor.author | Bang, Yung-Jue | - |
dc.date.accessioned | 2020-04-27T11:32:42Z | - |
dc.date.available | 2020-04-27T11:32:42Z | - |
dc.date.created | 2020-02-19 | - |
dc.date.created | 2020-02-19 | - |
dc.date.issued | 2012-12 | - |
dc.identifier.citation | American Journal of Clinical Oncology, Vol.35 No.6, pp.549-556 | - |
dc.identifier.issn | 0277-3732 | - |
dc.identifier.other | 91811 | - |
dc.identifier.uri | https://hdl.handle.net/10371/165490 | - |
dc.description.abstract | Objectives: Neuroendocrine tumor originates from several sites. This study was conducted to reveal the differences in clinical course of neuroendocrine tumors by the origin. Methods: We reviewed data of patients diagnosed with neuroendocrine tumor between January 1996 and July 2007. Results: A total of 371 patients were enrolled [pancreas 60, gastrointestinal (GI) tract 210, lung 35, other sites 46, unknown primary sites 20]. The primary tumor site correlated with the stage (P = 0.000) and grade (P = 0.000). At diagnosis, metastasis was observed in 28.3%, 6.7%, and 2.9% of the cases in pancreatic, GI, and pulmonary neuroendocrine tumors, respectively. Grade 3 neuroendocrine tumor was observed in 7.7%, 0.5%, and 0.0% in pancreatic, GI, and pulmonary neuroendocrine tumors. Overall survival was 116.0 months (95% confidence interval, 86.9-145.1). Overall survival was 116.0 months in pancreatic neuroendocrine tumor, not reached in GI neuroendocrine tumor and 120.0 months in pulmonary neuroendocrine tumor (P = 0.024). The recurrence rate was 18.0%. It was 20.9%, 11.9%, and 2.9% in pancreatic, GI, and pulmonary neuroendocrine tumors (P = 0.062). In multivariate analysis, stage, grade, and age were prognostic for overall survival (OS). Stage, grade, and sex were prognostic for disease-free survival. Conclusions: Neuroendocrine tumors from the pancreas, GI tract, and lung showed different clinical characteristics. | - |
dc.language | 영어 | - |
dc.publisher | Lippincott Williams & Wilkins Ltd. | - |
dc.title | Clinical Course of Neuroendocrine Tumors With Different Origins (the Pancreas, Gastrointestinal Tract, and Lung) | - |
dc.type | Article | - |
dc.contributor.AlternativeAuthor | 임석아 | - |
dc.identifier.doi | 10.1097/COC.0b013e31821dee0f | - |
dc.citation.journaltitle | American Journal of Clinical Oncology | - |
dc.identifier.wosid | 000311384000008 | - |
dc.identifier.scopusid | 2-s2.0-84870255588 | - |
dc.citation.endpage | 556 | - |
dc.citation.number | 6 | - |
dc.citation.startpage | 549 | - |
dc.citation.volume | 35 | - |
dc.identifier.sci | 000311384000008 | - |
dc.description.isOpenAccess | N | - |
dc.contributor.affiliatedAuthor | Oh, Do-Youn | - |
dc.contributor.affiliatedAuthor | Kim, Dong-Wan | - |
dc.contributor.affiliatedAuthor | Im, Seock-Ah | - |
dc.contributor.affiliatedAuthor | Kim, Tae-You | - |
dc.contributor.affiliatedAuthor | Heo, Dae Seog | - |
dc.contributor.affiliatedAuthor | Bang, Yung-Jue | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.subject.keywordPlus | PROGNOSTIC-FACTORS | - |
dc.subject.keywordPlus | LOW-GRADE | - |
dc.subject.keywordPlus | SURVIVAL | - |
dc.subject.keywordPlus | CLASSIFICATION | - |
dc.subject.keywordPlus | EPIDEMIOLOGY | - |
dc.subject.keywordPlus | NEOPLASMS | - |
dc.subject.keywordAuthor | neuroendocrine tumor | - |
dc.subject.keywordAuthor | origin | - |
dc.subject.keywordAuthor | treatment outcome | - |
dc.subject.keywordAuthor | prognosis | - |
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