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Updated: Mar 14, 2026

Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Sequential targeted therapy in synchronous dual-primary lung adenocarcinomas with EGFR and RET alterations: a 5-year
Yong-Liang Niu1, Ying Yang2, Xiao-Bao Teng1
1Department of Respiratory and Critical Care Medicine, No.2 People's Hospital of Fuyang City, Fuyang Infectious Disease Clinical College of Anhui Medical University, Fuyang, China.
Abstract:
With the increasing detection of multiple primary pulmonary nodules, accurately distinguishing between multiple primary lung cancers and intrapulmonary metastasis is crucial for diagnosis and treatment. We herein report a case of a 71-year-old female with bilateral multiple primary lung adenocarcinomas, in which separate lesions harbored an EGFR 19del mutation and a RET fusion gene, demonstrating intratumoral genetic heterogeneity. The patient was successively treated with an EGFR-TKI, chemotherapy, and the RET inhibitor pralsetinib, the latter of which maintained a response for over three years. Following the development of resistance, combination therapy with pralsetinib and anlotinib successfully achieved a partial response again. This case underscores the importance of comprehensive molecular testing across multiple lesions to guide precision therapy and provides clinical insights into RET fusion-positive lung cancer treatment and post-resistance combination strategies.
Insights
Distinguishing multiple primary lung cancers from metastasis is key. This case shows genetic differences in lung tumors, guiding targeted therapy and combination treatments after resistance develops.
Area of Science:
- Oncology
- Genetics
- Pulmonology
Background:
- Accurate diagnosis of multiple pulmonary nodules is critical for effective lung cancer treatment.
- Distinguishing multiple primary lung cancers from intrapulmonary metastasis presents a diagnostic challenge.
- Intratumoral genetic heterogeneity can influence treatment response in lung adenocarcinoma.
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