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Usefulness of complementary next-generation sequencing and quantitative immunohistochemistry panels for predicting brain metastases and selecting treatment outcomes of non-small cell lung cancer

dc.contributor.authorMachado-Rugolo, Juliana
dc.contributor.authorFabro, Alexandre Todorovic
dc.contributor.authorAscheri, Daniel
dc.contributor.authorFarhat, Cecilia
dc.contributor.authorAb'Saber, Alexandre Muxfeldt
dc.contributor.authorSa, Vanessa Karen de
dc.contributor.authorNagai, Maria Aparecida
dc.contributor.authorTakagaki, Teresa
dc.contributor.authorTerra, Ricardo
dc.contributor.authorParra, Edwin Roger
dc.contributor.authorCapelozzi, Vera Luiza
dc.contributor.institutionState Univ Soo Paulo
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionClin Hosp
dc.contributor.institutionInst Canc Sao Paulo
dc.contributor.institutionHeart Inst Incor
dc.contributor.institutionUniv Texas MD Anderson Canc Ctr
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2019-10-04T12:42:51Z
dc.date.available2019-10-04T12:42:51Z
dc.date.issued2019-01-01
dc.description.abstractTo demonstrate the usefulness of complementary next-generation sequencing (NGS) and immunohistochemistry (IHC) counting, we analyzed 196 patients with non-small cell lung cancer who underwent surgical resection and adjuvant chemotherapy. Formalin-fixed, paraffin-embedded samples of adenocarcinoma (ADC), squamous cell carcinoma, and large cell carcinoma were used to prepare tissue microarrays and were examined by protein H-score IHC image analysis and NGS for oncogenes and proto-oncogenes and genes of tumor suppressors, immune checkpoints, epithelial-mesenchymal transition factors, tyrosine kinase receptors, and vascular endothelial growth factors. In patients with brain metastases, primary tumors expressed lower PIK3CA protein levels. Overexpression of p53 and a higher PD-LI protein H-score were detected in patients who underwent surgical treatment followed by chemotherapy as compared with those who underwent only surgical treatment The absence of brain metastases was associated with wild-type sequences of genes EGFR, CD267, CTLA-4, and ZEBI. The combination of protein overexpression according to IHC and mutation according to NGS was rare (ie, represented by a very low percentage of concordant cases), except for p53 and vascular endothelial growth factor. Our data suggest that protein levels detected by IHC may be a useful complementary tool when mutations are not detected by NGS and also support the idea to expand this approach beyond ADC to include squamous cell carcinoma and even large cell carcinoma, particularly for patients with unusual clinical characteristics. Conversely, well-pronounced immunogenotypic features seemed to predict the clinical outcome after univariate and multivariate analyses. Patients with a solid ADC subtype and mutated genes EGFR, CTLA4, PDCDILG2, or ZEBI complemented with PD-L1 or p53 protein lower expression that only underwent surgical treatment who develop brain metastases may have the worst prognosis. (C) 2018 Elsevier Inc. All rights reserved.en
dc.description.affiliationState Univ Soo Paulo, Fac Med, Clin Hosp, BR-18618682 Botucatu, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Ribeirao Preto Sch Med, Dept Pathol & Legal Med, BR-14049900 Ribeirao Preto, Brazil
dc.description.affiliationUniv Sao Paulo, Med Sch, Dept Pathol, Lab Genom & Histomorphometry, BR-01246903 Sao Paulo, Brazil
dc.description.affiliationClin Hosp, Dept Oncol, BR-01246903 Sao Paulo, Brazil
dc.description.affiliationUniv Sao Paulo, Fac Med, Heart Inst Incor, Div Pneumol, BR-01246903 Sao Paulo, Brazil
dc.description.affiliationInst Canc Sao Paulo, Dept Thorac Surg, BR-01246903 Sao Paulo, Brazil
dc.description.affiliationHeart Inst Incor, Dept Thorac Surg, BR-01246903 Sao Paulo, Brazil
dc.description.affiliationUniv Texas MD Anderson Canc Ctr, Dept Translat Mol Pathol, Houston, TX 77030 USA
dc.description.sponsorshipUniversity of Texas Lung Specialized Programs of Research Excellence grant
dc.description.sponsorshipMD Anderson's Cancer Center Support Grant from National Cancer Institute
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipTechnology and Innovation of Brazil
dc.description.sponsorshipFoundation for the Support of Research of the State of Sao Paulo
dc.description.sponsorshipIdUniversity of Texas Lung Specialized Programs of Research Excellence grant: P50CA70907
dc.description.sponsorshipIdMD Anderson's Cancer Center Support Grant from National Cancer Institute: 2P3OCA016672
dc.description.sponsorshipIdTechnology and Innovation of Brazil: P246042/2012-5
dc.description.sponsorshipIdFoundation for the Support of Research of the State of Sao Paulo: FAPESP 2013/14277-4
dc.format.extent177-191
dc.identifierhttp://dx.doi.org/10.1016/j.humpath.2018.08.026
dc.identifier.citationHuman Pathology. Philadelphia: W B Saunders Co-elsevier Inc, v. 83, p. 177-191, 2019.
dc.identifier.doi10.1016/j.humpath.2018.08.026
dc.identifier.issn0046-8177
dc.identifier.urihttp://hdl.handle.net/11449/186211
dc.identifier.wosWOS:000459234800023
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofHuman Pathology
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectEpithelial-mesenchymal transition
dc.subjectImmunohistochemistry
dc.subjectNext-generation sequencing
dc.subjectH-score
dc.subjectAdenocarcinoma
dc.subjectSquamouscell carcinoma
dc.subjectLarge cell carcinoma
dc.titleUsefulness of complementary next-generation sequencing and quantitative immunohistochemistry panels for predicting brain metastases and selecting treatment outcomes of non-small cell lung canceren
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication

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