体细胞
精密医学
基因组
个性化医疗
基因
生物
免疫疗法
计算生物学
DNA测序
癌症
融合基因
医学
生物信息学
遗传学
作者
Liqun Wu,Herui Yao,Hui Chen,Aodi Wang,Kun Guo,Wenli Gou,Yanfei Yu,Xiang Li,Ming Yao,Shaohua Yuan,Fei Pang,Jinwei Hu,Lijuan Chen,Wenjin Liu,Jicheng Yao,Shuirong Zhang,Xiaowei Dong,Weifeng Wang,Jing Hu,Qi Ling
标识
DOI:10.1038/s41467-022-31780-9
摘要
Abstract Extending the benefits of tumor molecular profiling for all cancer patients requires a comprehensive analysis of tumor genomes across distinct patient populations worldwide. In this study, we perform deep next-generation DNA sequencing (NGS) from tumor tissues and matched blood specimens from over 10,000 patients in China by using a 450-gene comprehensive assay, developed and implemented under international clinical regulations. We perform a comprehensive comparison of somatically altered genes, the distribution of tumor mutational burden (TMB), gene fusion patterns, and the spectrum of various somatic alterations between Chinese and American patient populations. Here, we show 64% of cancers from Chinese patients in this study have clinically actionable genomic alterations, which may affect clinical decisions related to targeted therapy or immunotherapy. These findings describe the similarities and differences between tumors from Chinese and American patients, providing valuable information for personalized medicine.
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