Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/4828
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dc.contributor.authorMelo, Andreia Cristina de-
dc.contributor.authorSá, Vanessa Karen de-
dc.contributor.authorSternberg, Cinthya-
dc.contributor.authorOlivieri, Eloisa Ribeiro-
dc.contributor.authorCunha, Isabela Werneck da-
dc.contributor.authorFabro, Alexandre Todorovic-
dc.contributor.authorCarraro, Dirce Maria-
dc.contributor.authorSilva, Milton José de Barros e-
dc.contributor.authorInada, Haynna Kimie Pimenta-
dc.contributor.authorMello, Evandro Sobrosa de-
dc.contributor.authorSoares, Fernando Augusto-
dc.contributor.authorTakagaki, Tereza-
dc.contributor.authorFerreira, Carlos Gil Moreira-
dc.contributor.authorCapelozzi, Vera Luiza-
dc.date.accessioned2022-01-05T14:52:12Z-
dc.date.available2022-01-05T14:52:12Z-
dc.date.issued2015-
dc.identifier.citationMELO, Andreia Cristina de et al. Mutational Profile and New IASLC/ATS/ERS Classification Provide Additional Prognostic Information. Oncology, v. 89, p. 175–186, 2015.-
dc.identifier.issn1423-0232-
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/4828-
dc.descriptionp. 175–186.: tab. p&b.-
dc.description.abstractTo show additional prognostic information about the mutational profile and new International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society (IASLC/ATS/ERS) classification of adeno carcinoma (ADC) in patients without epidermal growth fac tor receptor (EGFR)-tyrosine kinase inhibitor treatments. Methods: In human lung ADC patients (n = 125), including 24 lepidic, 67 acinar, 23 papillary, and 11 solid predominant subtypes, EGFR and KRAS were sequenced, and anaplastic lymphoma kinase (ALK) rearrangements were screened us ing fluorescence in situ hybridization (FISH). Results: EGFR was mutated in 21.6% of patients with 19.57% showing a mean expression. The most frequent EGFR mutation was a deletion in exon 19, followed by an L858R amino acid substi tution in exon 21. KRAS was mutated in 26.4% of patients with 50% displaying mean expression. ALK rearrangement was detected in 6 patients (4.8%). Predominant acinar ADC was strongly associated with EGFR and KRAS mutation. Clin ical stage, lymph node metastases, and EGFR mutation in exon 18 showed a significant difference in disease-free and overall survival, but only a trend significance for EGFR and KRAS mutations. Multivariate analysis revealed that men aged >71 years, with a history of smoking (<72 packs/year), clinical stage I/II, and acinar histologic subtype presented better survival than women aged ≤ 71 years, with a history of smoking (>72 packs/year), and having a predominant solid ADC and EGFR mutation in exon 18. Conclusions: These re sults indicate that the mutational profile and new IASLC/ ATS/ERS classification provide additional prognostic infor mation about lung ADC.-
dc.publisherOncologypt_BR
dc.subjectAdenocarcinoma de Pulmãopt_BR
dc.subjectAdenocarcinoma of Lungpt_BR
dc.subjectMutaçãopt_BR
dc.subjectMutationpt_BR
dc.subjectGenes raspt_BR
dc.subjectGenes erbB-1pt_BR
dc.subjectPrognósticopt_BR
dc.subjectPrognosispt_BR
dc.subjectBrasilpt_BR
dc.subjectBrazilpt_BR
dc.titleMutational Profile and New IASLC/ATS/ERS Classification Provide Additional Prognostic Informationpt_BR
dc.TypeArticlept_BR
Appears in Collections:Artigos de Periódicos da área de Ginecologia



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