Prediction of TKI response in EGFR-mutant lung cancer patients-derived organoids using malignant pleural effusion

Author:

Lee Sang-HyunORCID,Kim Kyuhwan,Lee Eunyoung,Lee KyungminORCID,Ahn Kyeong Hwan,Park HansomORCID,Kim Yelim,Shin Soeun,Jeon Sang Youl,Hwang Yongki,Ahn Dong Hyuck,Kwon Yong-Jun,Moon Seok Whan,Moon Mi Hyoung,Kim Kyung Soo,Hyun Kwanyong,Kim Tae-JungORCID,Sung Yeoun Eun,Choi Joon YoungORCID,Park Chan Kwon,Kim Sung Won,Yeo Chang Dong,Sohn Hyun-Jung,Hyun You-SeokORCID,Kim Tai-Gyu,Ku Bosung,Lim Jeong Uk,Kim Seung JoonORCID

Abstract

AbstractPatient-derived organoids (PDOs) are valuable in predicting response to cancer therapy. PDOs are ideal models for precision oncologists. However, their practical application in guiding timely clinical decisions remains challenging. This study focused on patients with advanced EGFR-mutated non-small cell lung cancer and employed a cancer organoid-based diagnosis reactivity prediction (CODRP)-based precision oncology platform to assess the efficacy of EGFR inhibitor treatments. CODRP was employed to evaluate EGFR-tyrosine kinase inhibitors (TKI) drug sensitivity. The results were compared to those obtained using area under the curve index. This study validated this index by testing lung cancer-derived organoids in 14 patients with lung cancer. The CODRP index-based drug sensitivity test reliably classified patient responses to EGFR-TKI treatment within a clinically suitable 10-day timeline, which aligned with clinical drug treatment responses. This approach is promising for predicting and analyzing the efficacy of anticancer, ultimately contributing to the development of a precision medicine platform.

Publisher

Springer Science and Business Media LLC

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