Min Byung-Joo, Lee Woo Seung, Seo Myung-Eui, Lee Kye-Hwa, Jeong Seung-Yong, Ku Ja-Lok, Kim Yeul Hong, Shin Sang-Won, Kim Ju Han
DNA Analysis Division, National Forensic Service Seoul Institute, Seoul 08036, Korea.
Seoul National University Biomedical Informatics (SNUBI), Division of Biomedical Informatics, Seoul National University College of Medicine, Seoul 03080, Korea.
Cancers (Basel). 2021 Oct 12;13(20):5112. doi: 10.3390/cancers13205112.
Recently, several panels using two representative targeting methods have been developed but they do not reflect racial specificity, especially for Asians. We have developed and analytically validated the Korean Pan-cancer Companion Diagnostic (CDX) Panel to apply targeted anticancer drugs to Korean patients based on the molecular characteristics of tumors using tumor samples without matched patient normal samples. The panel included 31 genes with reported single nucleotide variants, 9 genes with reported copy number variations, and 15 genes with predictive responses to targeted drugs under clinical testing, enabling the panel to be analyzed for the targets of 30 targeted anticancer drugs. It is cost-effective and optimized for cancer type-specific therapy in Korean cancer patients across solid cancer types while minimizing the limitations of existing approaches. In addition, the optimized filtering protocol for somatic variants from tumor-only samples enables researchers to use this panel without matched normal samples. To verify the panel, 241 frozen tumor tissues and 71 formalin-fixed paraffin-embedded (FFPE) samples from several institutes were registered. This gene screening method is expected to reduce test turnaround time and cost, making it a balanced approach to investigate solid cancer-related gene regions.
最近,已经开发出了几种使用两种代表性靶向方法的检测板,但它们没有反映出种族特异性,尤其是对亚洲人而言。我们开发并通过分析验证了韩国泛癌伴随诊断(CDX)检测板,以便根据肿瘤的分子特征,使用未匹配患者正常样本的肿瘤样本,将靶向抗癌药物应用于韩国患者。该检测板包括31个具有报道的单核苷酸变异的基因、9个具有报道的拷贝数变异的基因以及15个在临床试验中对靶向药物有预测反应的基因,使得该检测板能够针对30种靶向抗癌药物的靶点进行分析。它具有成本效益,针对韩国实体癌类型的癌症患者进行癌症类型特异性治疗进行了优化,同时将现有方法的局限性降至最低。此外,针对仅肿瘤样本的体细胞变异的优化过滤方案使研究人员能够在没有匹配正常样本的情况下使用该检测板。为了验证该检测板,登记了来自几个机构的241个冷冻肿瘤组织和71个福尔马林固定石蜡包埋(FFPE)样本。这种基因筛查方法有望减少检测周转时间和成本,使其成为研究实体癌相关基因区域的一种平衡方法。