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LungBEAM: A prospective multicenter study to monitor stage IV NSCLC patients with EGFR mutations using BEAMing technology.
Garrido, Pilar; Paz-Ares, Luis; Majem, Margarita; Morán, Teresa; Trigo, José Manuel; Bosch-Barrera, Joaquim; Garcίa-Campelo, Rosario; González-Larriba, José Luis; Sánchez-Torres, José Miguel; Isla, Dolores; Viñolas, Núria; Camps, Carlos; Insa, Amelia; Juan, Óscar; Massuti, Bartomeu; Paredes, Alfredo; Artal, Ángel; López-Brea, Marta; Palacios, José; Felip, Enriqueta.
Afiliación
  • Garrido P; Medical Oncology Department, IRYCIS Hospital Universitario Ramón y Cajal, Universidad Alcalá, Madrid, Spain.
  • Paz-Ares L; CIBERONC, Madrid, Spain.
  • Majem M; CIBERONC, Madrid, Spain.
  • Morán T; Medical Oncology Department, Hospital Universitario 12 de Octubre and i+12 Research Institute, Madrid, Spain.
  • Trigo JM; Lung Cancer Group, Clinical Research Program, Spanish National Cancer Research Center (CNIO), Madrid, Spain.
  • Bosch-Barrera J; Complutense University, Madrid, Spain.
  • Garcίa-Campelo R; Medical Oncology Department, Hospital De La Santa Creu I Sant Pau, Barcelona, Spain.
  • González-Larriba JL; Spanish Lung Cancer Group (GECP), Barcelona, Spain.
  • Sánchez-Torres JM; Spanish Lung Cancer Group (GECP), Barcelona, Spain.
  • Isla D; ICO Badalona, Hospital Germans Trias i Pujol, Barcelona, Spain.
  • Viñolas N; Medical Oncology Department, Hospital Universitario Virgen de la Victoria, Málaga, Spain.
  • Camps C; Medical Oncology, Catalan Institute of Oncology (ICO), Dr. Josep Trueta Hospital of Girona, Girona, Spain.
  • Insa A; Medical Oncology Department, Hospital Universitario Da Coruña, A Coruña, Spain.
  • Juan Ó; Medical Oncology Department, Hospital Universitario Clínico San Carlos, Madrid, Spain.
  • Massuti B; Medical Oncology Department, Hospital de la Princesa, Madrid, Spain.
  • Paredes A; Medical Oncology Department, Hospital Universitario Lozano Blesa, Zaragoza, Spain.
  • Artal Á; Medical Oncology Department, Hospital Clinic i Provincial, Barcelona, Spain.
  • López-Brea M; CIBERONC, Madrid, Spain.
  • Palacios J; Medical Oncology Department, Hospital General Universitario de Valencia, Universidad de Valencia, Valencia, Spain.
  • Felip E; Medical Oncology Department, Hospital Clínico Universitario, Valencia, Spain.
Cancer Med ; 10(17): 5878-5888, 2021 09.
Article en En | MEDLINE | ID: mdl-34296539
ABSTRACT

OBJECTIVES:

The aim of LungBEAM was to determine the value of a novel epidermal growth factor receptor (EGFR) mutation test in blood based on BEAMing technology to predict disease progression in advanced non-small cell lung cancer (NSCLC) patients treated with first- or second-generation EGFR-tyrosine kinase inhibitors (EGFR-TKIs). Another goal was to monitor the dynamics of EGFR mutations, as well as to track EGFR exon 20 p.T790M (p.T790M) resistance during treatment, as critical indicators of therapeutic efficacy and patient survival.

METHODS:

Stage IV NSCLC patients with locally confirmed EGFR-TKI sensitizing mutations (ex19del and/or L858R) in biopsy tissue who were candidates to receive first- or second-generation EGFR-TKI as first-line therapy were included. Plasma samples were obtained at baseline and every 4 weeks during treatment until a progression-free survival (PFS) event or until study completion (72-week follow-up). The mutant allele fraction (MAF) was determined for each identified mutation using BEAMing.

RESULTS:

A total of 68 of the 110 (61.8%) patients experienced a PFS event. Twenty-six patients (23.6%) presented with an emergent p.T790M mutation in plasma at some point during follow-up, preceding radiologic progression with a median of 76 (interquartile ratio 54-111) days. Disease progression correlated with the appearance of p.T790M in plasma with a hazard ratio (HR) of 1.94 (95% confidence interval [CI], 1.48-2.54; p < 0.001). The HR for progression in patients showing increasing plasma sensitizing mutation levels (positive MAF slope) versus patients showing either decreasing or unchanged plasma mutation levels (negative or null MAF slopes) was 3.85 (95% CI, 2.01-7.36; p < 0.001).

CONCLUSION:

Detection and quantification of EGFR mutations in circulating tumor DNA using the highly sensitive BEAMing method should greatly assist in optimizing treatment decisions for advanced NSCLC patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Cancer Med Año: 2021 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Cancer Med Año: 2021 Tipo del documento: Article País de afiliación: España