Personalized treatment of HER2-positive lung adenocarcinoma using Human Organoid Drug Sensitivity Test.
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OpenAlex 토픽 ·
HER2/EGFR in Cancer Research
Lung Cancer Treatments and Mutations
Advanced Biosensing Techniques and Applications
Human Epidermal Growth Factor Receptor 2 (HER2) mutations account for approximately 3% of non-small cell lung cancer (NSCLC) patients.
APA
Tao Luan, Suneng Fu, et al. (2026). Personalized treatment of HER2-positive lung adenocarcinoma using Human Organoid Drug Sensitivity Test.. Human vaccines & immunotherapeutics, 22(1), 2629081. https://doi.org/10.1080/21645515.2026.2629081
MLA
Tao Luan, et al.. "Personalized treatment of HER2-positive lung adenocarcinoma using Human Organoid Drug Sensitivity Test.." Human vaccines & immunotherapeutics, vol. 22, no. 1, 2026, pp. 2629081.
PMID
41700896
Abstract
Human Epidermal Growth Factor Receptor 2 (HER2) mutations account for approximately 3% of non-small cell lung cancer (NSCLC) patients. Currently, targeted therapies for HER2-mutant NSCLC include HER2 tyrosine kinase inhibitors (TKIs) and HER2 Antibody-drug conjugates (ADC). However, resistance often develops, and effective treatments for HER2 mutations remain lacking. We report a case of HER2-mutant lung adenocarcinoma where the patient developed resistance and severe interstitial lung disease following antibody-drug conjugate therapy. A highly biomimetic Human Organoid (HO) platform was employed to screen potential therapeutic options for the patient. The HO results indicated efficacy of Sunvozertinib and ineffectiveness of ADC, with maximum half-maximal inhibitory concentration (IC) values of 0.28 and 2.96, respectively. This case demonstrates the potential of Human Organoid Drug Sensitivity Test (HO-DST) to guide effective salvage therapy, bridging the gap between genomic profiling and functional drug response in precision oncology.
MeSH Terms
Humans; Erb-b2 Receptor Tyrosine Kinases; Organoids; Adenocarcinoma of Lung; Precision Medicine; Lung Neoplasms; Antineoplastic Agents; Drug Resistance, Neoplasm; Immunoconjugates; Female; Protein Kinase Inhibitors; Mutation