Cancer organoid-based diagnosis reactivity prediction (CODRP) index-based anticancer drug sensitivity test in ALK-rearrangement positive non-small cell lung cancer (NSCLC)

肺癌 医学 癌症 阿列克替尼 克里唑蒂尼 间变性淋巴瘤激酶 曲线下面积 内科学 肿瘤科 癌细胞 癌症研究 恶性胸腔积液
作者
Sang‐Yun Lee,Hyeong Jun Cho,Jimin Choi,Bosung Ku,Seok Whan Moon,Mi Hyoung Moon,Kyung Soo Kim,Kwanyong Hyun,Tae Jung Kim,Yeoun Eun Sung,Yongki Hwang,Eunyoung Lee,Dong Hyuck Ahn,Joon Young Choi,Jeong Uk Lim,Chan Kwon Park,Sung Won Kim,Seung Joon Kim,In-Seong Koo,Woo Seok Jung
出处
期刊:Journal of Experimental & Clinical Cancer Research [BioMed Central]
卷期号:42 (1): 309-309 被引量:15
标识
DOI:10.1186/s13046-023-02899-4
摘要

Abstract Background Recently, cancer organoid-based drug sensitivity tests have been studied to predict patient responses to anticancer drugs. The area under curve (AUC) or IC 50 value of the dose-response curve (DRC) is used to differentiate between sensitive and resistant patient‘s groups. This study proposes a multi-parameter analysis method (cancer organoid-based diagnosis reactivity prediction, CODRP) that considers the cancer stage and cancer cell growth rate, which represent the severity of cancer patients, in the sensitivity test. Methods On the CODRP platform, patient-derived organoids (PDOs) that recapitulate patients with lung cancer were implemented by applying a mechanical dissociation method capable of high yields and proliferation rates. A disposable nozzle-type cell spotter with efficient high-throughput screening (HTS) has also been developed to dispense a very small number of cells due to limited patient cells. A drug sensitivity test was performed using PDO from the patient tissue and the primary cancer characteristics of PDOs were confirmed by pathological comparision with tissue slides. Results The conventional index of drug sensitivity is the AUC of the DRC. In this study, the CODRP index for drug sensitivity test was proposed through multi-parameter analyses considering cancer cell proliferation rate, the cancer diagnosis stage, and AUC values. We tested PDOs from eight patients with lung cancer to verify the CODRP index. According to the anaplastic lymphoma kinase (ALK) rearrangement status, the conventional AUC index for the three ALK-targeted drugs (crizotinib, alectinib, and brigatinib) did not classify into sensitive and resistant groups. The proposed CODRP index-based drug sensitivity test classified ALK-targeted drug responses according to ALK rearrangement status and was verified to be consistent with the clinical drug treatment response. Conclusions Therefore, the PDO-based HTS and CODRP index drug sensitivity tests described in this paper may be useful for predicting and analyzing promising anticancer drug efficacy for patients with lung cancer and can be applied to a precision medicine platform.
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