Application of Comprehensive Genomic Profiling-Based Next-Generation Sequencing Assay to Improve Cancer Care in a Developing Country

Fecha de publicación:

Autores organización

  • Luis Leonardo Rojas Beltran

    Autor

  • Andres Felipe Cardona Mendoza

    Autor

Autores

  • Cifuentes C.
  • Lombana M.
  • Vargas H.
  • Laguado P.
  • Ruiz-Patiño A.
  • Navarro U.
  • Vargas C.
  • Ricaurte L.
  • Arrieta O.
  • Zatarain-Barron L.
  • Zapata L.
  • González G.
  • Ortiz C.
  • Bernal L.
  • Restrepo J.G.
  • Viola L.
  • Grosso F.
  • Zapata R.
  • Mantilla W.
  • Carranza H.
  • Bustillo I.
  • Llinas N.
  • Duarte R.
  • Rodríguez J.
  • Archila P.
  • Ávila J.
  • Bermúdez M.
  • Gámez T.
  • Sotelo C.
  • Otero J.
  • Forero E.
  • Lema M.
  • Limpias C.
  • Ordóñez-Reyes C.
  • Mejía S.
  • Rolfo C.
  • Rosell R.

Grupos de investigación

Resumen

Purpose: Identifying actionable oncogenic mutations have changed the therapeutic landscape in different types of tumors. This study investigated the utility of comprehensive genomic profiling (CGP), a hybrid capture-based next-generation sequencing (NGS) assay, in clinical practice in a developing country. Methods: In this retrospective cohort study, CGP was performed on clinical samples from patients with different solid tumors recruited between December 2016 and November 2020, using hybrid capture-based genomic profiling, at the individual treating physicians’ request in the clinical care for therapy decisions. Kaplan–Meier survival curves were estimated to characterize the time-to-event variables. Results: Patients median age was 61 years (range: 14–87 years), and 64.7% were female. The most common histological diagnosis was lung primary tumors, with 90 patients corresponding to 52.9% of the samples (95% CI 45.4-60.4%). Actionable mutations with FDA-approved medications for specific alterations correspondent to tumoral histology were identified in 58 cases (46.4%), whereas other alterations were detected in 47 different samples (37.6%). The median overall survival was 15.5 months (95% CI 11.7 months-NR). Patients who were subjected to genomic evaluation at diagnosis reached a median overall survival of 18.3 months (95% CI 14.9 months-NR) compared to 14.1 months (95% CI 11.1 months-NR) in patients who obtained genomic evaluation after tumor progression and during standard treatment (P =.7). Conclusion: CGP of different types of tumors identifies clinically relevant genomic alterations that have benefited from targeted therapy and improve cancer care in a developing country to guide personalized treatment to beneficial outcomes of cancer patients. © The Author(s) 2023.

Datos de la publicación

ISSN/ISSNe:
1073-2748, 1526-2359

Cancer Control  SAGE Publications Ltd

Tipo:
Article
Páginas:
-
Enlace a otro recurso:
www.scopus.com

Citas Recibidas en Scopus: 3

Documentos

  • No hay documentos

Métricas

Filiaciones mostrar / ocultar

Keywords

  • Developing Countries; Female; Genomics; High-Throughput Nucleotide Sequencing; Humans; Lung Neoplasms; Male; Middle Aged; Mutation; Retrospective Studies; antineoplastic metal complex; atezolizumab; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor; pembrolizumab; pemetrexed; adolescent; adult; aged; Article; cancer patient; cancer therapy; cohort analysis; comprehensive genomic profiling; controlled study; developing country; female; Food and Drug Administration; gene mutation; genetic profile; high throughput sequencing; histology; human; Kaplan Meier method; lung tumor; major clinical study; male; oncogenomics; overall survival; personalized medicine; primary tumor; retrospective study; solid tumor; tumor growth; developed country; genomics; high throughput sequencing; lung tumor; middle aged; mutation; pathology

Campos de estudio

Financiación

Citar la publicación

Compartir la publicación