Cited 61 times in

Genetic and clinicopathologic characteristics of lung adenocarcinoma with tumor spread through air spaces

DC Field Value Language
dc.contributor.author김문식-
dc.contributor.author심효섭-
dc.contributor.author이재석-
dc.date.accessioned2018-10-11T08:54:34Z-
dc.date.available2018-10-11T08:54:34Z-
dc.date.issued2018-
dc.identifier.issn0169-5002-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/163454-
dc.description.abstractOBJECTIVE: The World Health Organization Classification of Lung Tumors considers "Spread Through Air Spaces (STAS)" as a form of invasion in lung adenocarcinoma. However, its existence as an independent pathologic entity rather than an artifact caused by spreading through a knife surface is still controversial. Therefore, we performed comprehensive analyses on the genetic and clinicopathologic characteristics of lung adenocarcinoma with STAS. MATERIALS AND METHODS: A total of 316 surgically resected lung adenocarcinoma cases were analyzed retrospectively. Detailed analyses were performed on clinical-histological-molecular features. Tumor STAS was defined as tumor cells within air spaces in the lung parenchyma beyond the edge of the main tumor. RESULTS: STAS was observed in 160 cases (50.6%). STAS was significantly related to lymphovascular invasion, lymph node metastasis, higher stage, and high-grade histologic subtype. STAS was frequently found in tumors with wild-type EGFR or ALK-rearrangement. Logistic regression analysis showed that STAS was significantly associated with absence of lepidic component, presence of micropapillary component, cribriform predominant type, lymphovascular invasion, and wild-type EGFR. Multivariate survival analysis demonstrated that STAS was independently associated with shorter recurrence-free survival. STAS was also associated with recurrences to extrathoracic sites as well as intrathoracic sites. CONCLUSION: STAS is associated with certain pathological and molecular subtypes. STAS might be a parameter for tumor aggressiveness in that it is strongly associated with poor prognostic factors and recurrence, including to extrathoracic sites.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier Scientific Publishers-
dc.relation.isPartOfLUNG CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleGenetic and clinicopathologic characteristics of lung adenocarcinoma with tumor spread through air spaces-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry-
dc.contributor.departmentDept. of Pathology-
dc.contributor.googleauthorJae Seok Lee-
dc.contributor.googleauthorEun Kyung Kim-
dc.contributor.googleauthorMoonsik Kim-
dc.contributor.googleauthorHyo Sup Shim-
dc.identifier.doi10.1016/j.lungcan.2018.07.020-
dc.contributor.localIdA05557-
dc.contributor.localIdA02219-
dc.contributor.localIdA03072-
dc.relation.journalcodeJ02174-
dc.identifier.eissn1872-8332-
dc.identifier.pmid30089582-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S016950021830480X-
dc.subject.keywordAdenocarcinoma-
dc.subject.keywordGenetic-
dc.subject.keywordLung cancer-
dc.subject.keywordPathological-
dc.subject.keywordRecurrence-
dc.subject.keywordSpread through air spaces-
dc.contributor.alternativeNameKim, Moonsik-
dc.contributor.alternativeNameShim, Hyo Sup-
dc.contributor.alternativeNameLee, Jae Seok-
dc.contributor.affiliatedAuthorKim, Moonsik-
dc.contributor.affiliatedAuthorShim, Hyo Sup-
dc.contributor.affiliatedAuthorLee, Jae Seok-
dc.citation.volume123-
dc.citation.startPage121-
dc.citation.endPage126-
dc.identifier.bibliographicCitationLUNG CANCER, Vol.123 : 121-126, 2018-
dc.identifier.rimsid60403-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.