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Identification of a high-risk group for brain metastases in non-small cell lung cancer patients.
Cacho-Díaz, Bernardo; Cuapaténcatl, Laura Denisse; Rodríguez, Jose Antonio; Garcilazo-Reyes, Ytel Jazmin; Reynoso-Noverón, Nancy; Arrieta, Oscar.
Afiliação
  • Cacho-Díaz B; Neuro Oncology Unit, National Cancer Institute, San Fernando 22, Tlalpan, 14080, Mexico City, ZC, Mexico. bernardocacho@doctor.com.
  • Cuapaténcatl LD; Neuro Oncology Unit, National Cancer Institute, San Fernando 22, Tlalpan, 14080, Mexico City, ZC, Mexico.
  • Rodríguez JA; Neuro Oncology Unit, National Cancer Institute, San Fernando 22, Tlalpan, 14080, Mexico City, ZC, Mexico.
  • Garcilazo-Reyes YJ; Neuro Oncology Unit, National Cancer Institute, San Fernando 22, Tlalpan, 14080, Mexico City, ZC, Mexico.
  • Reynoso-Noverón N; Research Department, National Cancer Institute, Mexico City, Mexico.
  • Arrieta O; Thoracic Oncology Unit, National Cancer Institute, Mexico City, Mexico. ogarrieta@gmail.com.
J Neurooncol ; 155(1): 101-106, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34546499
PURPOSE: Identification of a high-risk group of brain metastases (BM) in patients with non-small cell lung cancer (NSCLC) could lead to early interventions and probably better prognosis. The objective of the study was to identify this group by generating a multivariable model with recognized and accessible risk factors. METHODS: A retrospective cohort from patients seen at a single center during 2010-2020, was divided into a training (TD) and validation (VD) datasets, associations with BM were measured in the TD with logit, variables significantly associated were used to generate a multivariate model. Model´s performance was measured with the AUC/C-statistic, Akaike information criterion, and Brier score. RESULTS: From 570 patients with NSCLC who met the strict eligibility criteria a TD and VD were randomly assembled, no significant differences were found amid both datasets. Variables associated with BM in the multivariate logit analyses were age [P 0.001, OR 0.96 (95% CI 0.93-0.98)]; mutational status positive [P 0.027, OR 1.96 (95% CI 1.07-3.56); and carcinoembryonic antigen levels [P 0.016, OR 1.001 (95% CI 1.000-1.003). BM were diagnosed in 24% of the whole cohort. Stratification into a high-risk group after simplification of the model, displayed a frequency of BM of 63% (P < 0.001). CONCLUSION: A multivariate model comprising age, carcinoembryonic antigen levels, and mutation status allowed the identification of a truly high-risk group of BM in NSCLC patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article