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Analysis of genomic alternations in epidermal growth factor receptor (EGFR)-T790M-mutated non-small cell lung cancer (NSCLC) patients with acquired resistance to osimertinib therapy.
Hsu, Ping-Chih; Chang, John Wen-Cheng; Chiu, Li-Chung; Yang, Cheng-Ta; Kuo, Scott Chih-Hsi; Fang, Yueh-Fu; Wu, Chiao-En.
Affiliation
  • Hsu PC; Division of Thoracic Oncology, Department of Thoracic Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, 33305, Taiwan.
  • Chang JW; Department of Medicine, College of Medicine, Chang Gung University, Taoyuan, 33302, Taiwan.
  • Chiu LC; Department of Medicine, College of Medicine, Chang Gung University, Taoyuan, 33302, Taiwan.
  • Yang CT; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, 5, Fu-Hsing Street, Kwei-Shan, Taoyuan, 33305, Taiwan.
  • Kuo SC; Division of Thoracic Oncology, Department of Thoracic Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, 33305, Taiwan.
  • Fang YF; Department of Medicine, College of Medicine, Chang Gung University, Taoyuan, 33302, Taiwan.
  • Wu CE; Division of Thoracic Oncology, Department of Thoracic Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, 33305, Taiwan.
Clin Transl Oncol ; 2024 Sep 24.
Article in En | MEDLINE | ID: mdl-39317868
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Genomic alterations after resistance to osimertinib therapy in advanced T790M-mutated non-small cell lung cancer (NSCLC) are complex and poorly understood. In this study, we aimed to detect these genomic alternations via comprehensive next-generation sequencing (NGS) of tissue and liquid biopsies. PATIENTS AND

METHODS:

From September 2020 to June 2021, 31 stage IIIB/IV T790M-mutated NSCLC patients who exhibited progressive disease after osimertinib therapy and provided written informed consent were recruited. Liquid and tissue biopsy samples for NGS testing were collected from 31 and 18 patients, respectively. Eighteen study patients had paired NGS data from tissue and liquid biopsies.

RESULTS:

With respect to the T790M mutation status, the preservation and loss rates were 33% and 67%, respectively, in both liquid and tissue biopsy samples. Five patients (16.1%) had the C797S mutation (4 liquid samples and 1 tissue sample). Two (6.5%) had MET mutations, 3 (9.7%) had BRAF-V600E mutations, and 1 (3.2%) had a KRAS-G12C mutation. Among the 18 patients who underwent tissue rebiopsies, those with preserved T790M mutation had significantly longer progression-free survival (PFS) with osimertinib therapy than those with T790M mutation loss (10.8 vs. 5.0 months, P = 0.045). Among all patients, those with T790M mutation loss in liquid biopsy samples had longer PFS after osimertinib therapy (10.8 vs. 7.5 months, P = 0.209) and postprogression survival (17.7 vs. 9.6 months, P = 0.132) than those with preserved T790M mutation based on liquid biopsies.

CONCLUSIONS:

NGS using either tissue or liquid biopsy samples from advanced T790M-mutated NSCLC patients with acquired resistance to osimertinib therapy can detect various genomic alternations. Future studies focusing on subsequent tailored therapies on the basis of NGS results are warranted.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Transl Oncol Year: 2024 Document type: Article Affiliation country: Taiwán Country of publication: Italia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Transl Oncol Year: 2024 Document type: Article Affiliation country: Taiwán Country of publication: Italia