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Benefits of NGS in Advanced Lung Adenocarcinoma Vary by Populations and Timing of Examination.
Lee, Po-Hsin; Ou, Wei-Fan; Huang, Yen-Hsiang; Hsu, Kuo-Hsuan; Tseng, Jeng-Sen; Chang, Gee-Chen; Yang, Tsung-Ying.
Afiliación
  • Lee PH; Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
  • Ou WF; School of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Huang YH; Doctoral Program in Translational Medicine, National Chung Hsing University, Taichung 402, Taiwan.
  • Hsu KH; Rong Hsing Translational Medicine Research Center, National Chung Hsing University, Taichung 402, Taiwan.
  • Tseng JS; Institute of Biomedical Sciences, National Chung Hsing University, Taichung 402, Taiwan.
  • Chang GC; Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
  • Yang TY; Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
Int J Mol Sci ; 25(13)2024 Jun 25.
Article en En | MEDLINE | ID: mdl-39000058
ABSTRACT
Despite the widespread application of next-generation sequencing (NGS) in advanced lung adenocarcinoma, its impact on survival and the optimal timing for the examination remain uncertain. This cohort study included advanced lung adenocarcinoma patients who underwent NGS testing. We categorized patients into four groups Group 1 treatment-naïve, upfront NGS; Group 2 Treatment-naïve, exclusionary EGFR/ALK/ROS1; Group 3 post-treatment, no known EGFR/ALK/ROS1; Group 4 known driver mutation and post-TKI treatment. A total of 424 patients were included. There were 128, 126, 90, and 80 patients in Groups 1, 2, 3, and 4, respectively. In Groups 1, 2, 3, and 4, targetable mutations were identified in 76.6%, 49.2%, 41.1%, and 33.3% of the patients, respectively (p < 0.001). Mutation-targeted treatments were applied in 68.0%, 15.1%, 27.8%, and 22.5% of the patients, respectively (p < 0.001). In the overall population, patients receiving mutation-targeted treatments exhibited significantly longer overall survival (OS) (aHR 0.54 [95% CI 0.37-0.79], p = 0.001). The most profound benefit was seen in the Group 1 patients (not reached vs. 40.4 months, p = 0.028). The median OS of patients with mutation-targeted treatments was also significantly longer among Group 2 patients. The median post-NGS survival of patients receiving mutation-targeted treatments was numerically longer in Group 3 and Group 4 patients. In conclusion, mutation-targeted therapy is associated with a favorable outcome. However, the opportunities of NGS-directed treatment and the survival benefits of mutation-targeted treatment were various among different populations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Secuenciación de Nucleótidos de Alto Rendimiento / Adenocarcinoma del Pulmón / Neoplasias Pulmonares / Mutación Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Secuenciación de Nucleótidos de Alto Rendimiento / Adenocarcinoma del Pulmón / Neoplasias Pulmonares / Mutación Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán