<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(11)</volume><submitter>Alves Pinto I</submitter><funding>AstraZeneca do Brasil Ltda</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Targeted and immunotherapies are currently moving toward early-stage settings for patients with non-small cell lung cancer (NSCLC). Predictive biomarkers data are scarce in this scenario. We aimed to describe the frequency of EGFR mutations and PD-L1 expression levels in early-stage non-squamous patients with NSCLC from a large, single Brazilian oncology center.&lt;h4>Methods&lt;/h4>We retrospectively evaluated patients with NSCLC diagnosed at an early-stage (IB to IIIA-AJCC seventh edition) at Barretos Cancer Hospital (n = 302). EGFR mutational status was assessed in FFPE tumor tissues using distinct methodologies (NGS, Cobas, or Sanger sequencing). PD-L1 expression was evaluated by immunohistochemistry (clone 22C3) and reported as Tumor Proportion Score (TPS), categorized as</pubmed_abstract><journal>The oncologist</journal><pagination>e899-e907</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9632322</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>EGFR Mutations and PD-L1 Expression in Early-Stage Non-Small Cell Lung Cancer: A Real-World Data From a Single Center in Brazil.</pubmed_title><pmcid>PMC9632322</pmcid><pubmed_authors>Oliveira da Silva M</pubmed_authors><pubmed_authors>Biazotto Fernandes MF</pubmed_authors><pubmed_authors>Berardinelli GN</pubmed_authors><pubmed_authors>Jacinto AA</pubmed_authors><pubmed_authors>Junqueira Pinto GD</pubmed_authors><pubmed_authors>de Oliveira Cavagna R</pubmed_authors><pubmed_authors>Virginio da Silva AL</pubmed_authors><pubmed_authors>Negreiros IS</pubmed_authors><pubmed_authors>Duval da Silva V</pubmed_authors><pubmed_authors>Reis RM</pubmed_authors><pubmed_authors>Albino da Silva EC</pubmed_authors><pubmed_authors>Dias JM</pubmed_authors><pubmed_authors>Santiago Goncalves MF</pubmed_authors><pubmed_authors>Leal LF</pubmed_authors><pubmed_authors>de Oliveira MA</pubmed_authors><pubmed_authors>Alves Pinto I</pubmed_authors><pubmed_authors>Ferreira da Silva FA</pubmed_authors><pubmed_authors>Souza LC</pubmed_authors><pubmed_authors>de Paula FE</pubmed_authors><pubmed_authors>Casagrande GMS</pubmed_authors><pubmed_authors>Santana IV</pubmed_authors><pubmed_authors>De Marchi P</pubmed_authors></additional><is_claimable>false</is_claimable><name>EGFR Mutations and PD-L1 Expression in Early-Stage Non-Small Cell Lung Cancer: A Real-World Data From a Single Center in Brazil.</name><description>&lt;h4>Background&lt;/h4>Targeted and immunotherapies are currently moving toward early-stage settings for patients with non-small cell lung cancer (NSCLC). Predictive biomarkers data are scarce in this scenario. We aimed to describe the frequency of EGFR mutations and PD-L1 expression levels in early-stage non-squamous patients with NSCLC from a large, single Brazilian oncology center.&lt;h4>Methods&lt;/h4>We retrospectively evaluated patients with NSCLC diagnosed at an early-stage (IB to IIIA-AJCC seventh edition) at Barretos Cancer Hospital (n = 302). EGFR mutational status was assessed in FFPE tumor tissues using distinct methodologies (NGS, Cobas, or Sanger sequencing). PD-L1 expression was evaluated by immunohistochemistry (clone 22C3) and reported as Tumor Proportion Score (TPS), categorized as</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-07-14T16:04:14.094Z</modification><creation>2024-11-08T20:16:10.234Z</creation></dates><accession>S-EPMC9632322</accession><cross_references><pubmed>36099421</pubmed><doi>10.1093/oncolo/oyac167</doi></cross_references></HashMap>