Cited 0 times in
Correlation Between 18F-Fluorodeoxyglucose Uptake and Epidermal Growth Factor Receptor Mutations in Advanced Lung Cancer
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 조병철 | - |
dc.contributor.author | 조응혁 | - |
dc.contributor.author | 강원준 | - |
dc.contributor.author | 윤미진 | - |
dc.contributor.author | 이재훈 | - |
dc.contributor.author | 이종두 | - |
dc.contributor.author | 전태주 | - |
dc.date.accessioned | 2014-12-19T17:31:23Z | - |
dc.date.available | 2014-12-19T17:31:23Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 1869-3474 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/91567 | - |
dc.description.abstract | Purpose Mutations in the epidermal growth factor receptor (EGFR) gene have been identified as potential targets for the treatment and prognostic factors for non-small cell lung cancer (NSCLC). We assessed the correlation between fluorodeoxyglucose (FDG) uptake and EGFR mutations, as well as their prognostic implications. Methods A total of 163 patients with pathologically confirmed NSCLC were enrolled (99 males and 64 females; median age, 60 years). All patients underwent FDG positron emission tomography before treatment, and genetic studies of EGFR mutations were performed. The maximum standardized uptake value (SUVmax) of the primary lung cancer was measured and normalized with regard to liver uptake. The SUVmax between the wild-type and EGFR mutant groups was compared. Survival was evaluated according to SUVmax and EGFR mutation status. Results EGFR mutations were found in 57 patients (60.8 %). The SUVmax tended to be higher in wild-type than mutant tumors, but was not significantly different (11.1 ± 5.7 vs. 9.8 ± 4.4, P = 0.103). The SUVmax was significantly lower in patients with an exon 19 mutation than in those with either an exon 21 mutation or wild type (P = 0.003 and 0.009, respectively). The EGFR mutation showed prolonged overall survival (OS) compared to wild-type tumors (P = 0.004). There was no significant difference in survival according to SUVmax. Both OS and progression-free survival of patients with a mutation in exon 19 were significant longer than in patients with wild-type tumors. Conclusion In patients with NSCLC, a mutation in exon 19 was associated with a lower SUVmax and is a reliable predictor for good survival. | - |
dc.description.statementOfResponsibility | open | - |
dc.relation.isPartOf | NUCLEAR MEDICINE AND MOLECULAR IMAGING | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Correlation Between 18F-Fluorodeoxyglucose Uptake and Epidermal Growth Factor Receptor Mutations in Advanced Lung Cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학) | - |
dc.contributor.googleauthor | Yun-Jung Choi | - |
dc.contributor.googleauthor | Byoung Chul Cho | - |
dc.contributor.googleauthor | Yong Hyu Jeong | - |
dc.contributor.googleauthor | Hyo Jung Seo | - |
dc.contributor.googleauthor | Hyun Jeong Kim | - |
dc.contributor.googleauthor | Arthur Cho | - |
dc.contributor.googleauthor | Jae Hoon Lee | - |
dc.contributor.googleauthor | Mijin Yun | - |
dc.contributor.googleauthor | Tae Joo Jeon | - |
dc.contributor.googleauthor | Jong Doo Lee | - |
dc.contributor.googleauthor | Won Jun Kang | - |
dc.identifier.doi | 24900056 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00062 | - |
dc.contributor.localId | A03822 | - |
dc.contributor.localId | A03887 | - |
dc.contributor.localId | A02550 | - |
dc.contributor.localId | A03138 | - |
dc.contributor.localId | A03093 | - |
dc.contributor.localId | A03557 | - |
dc.contributor.localId | A05554 | - |
dc.contributor.localId | A05646 | - |
dc.relation.journalcode | J02383 | - |
dc.identifier.eissn | 1869-3482 | - |
dc.identifier.pmid | 24900056 | - |
dc.identifier.url | http://link.springer.com/article/10.1007/s13139-012-0142-z# | - |
dc.subject.keyword | 18F-fluoro-2-deoxy-D-glucose positron emission tomography (18F-FDG PET) | - |
dc.subject.keyword | Epidermal growth factor receptor (EGFR) gene | - |
dc.subject.keyword | Non-small cell lung cancer | - |
dc.contributor.alternativeName | Cho, Byoung Chul | - |
dc.contributor.alternativeName | Cho, Arthur Eung Hyuck | - |
dc.contributor.alternativeName | Kang, Won Jun | - |
dc.contributor.alternativeName | Yun, Mi Jin | - |
dc.contributor.alternativeName | Lee, Jae Hoon | - |
dc.contributor.alternativeName | Lee, Jong Doo | - |
dc.contributor.alternativeName | Jeon, Tae Joo | - |
dc.contributor.affiliatedAuthor | Kang, Won Jun | - |
dc.contributor.affiliatedAuthor | Cho, Byoung Chul | - |
dc.contributor.affiliatedAuthor | Cho, Arthur Eung Hyuck | - |
dc.contributor.affiliatedAuthor | Yun, Mi Jin | - |
dc.contributor.affiliatedAuthor | Lee, Jong Doo | - |
dc.contributor.affiliatedAuthor | Lee, Jae Hoon | - |
dc.contributor.affiliatedAuthor | Jeon, Tae Joo | - |
dc.contributor.affiliatedAuthor | Jeong, Yong Hyu | - |
dc.citation.volume | 46 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 169 | - |
dc.citation.endPage | 175 | - |
dc.identifier.bibliographicCitation | NUCLEAR MEDICINE AND MOLECULAR IMAGING, Vol.46(3) : 169-175, 2012 | - |
dc.identifier.rimsid | 29309 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.