Nishihara Hiroshi
Rinsho Byori. 2017 Feb;65(2):167-172.
The development of genomic medicine has enabled us to perform contemporary clinical sequencing, while the acquisition of high-quality biospecimens and the appropriate handling of these materials are indispensable. We started Clinical Biobank, a novel system for on-demand-type banking, in 2014. During the 22 months from August 2014, we stored around 6,000 biospecimens from 1,700 patients, and most of them were obtained for diverse clinical research. The quality and amount of extracted DNA and RNA from PFPE samples were markedly high; thus, these samples are adequate for targeted amplicon sequencing using MiSeq (Illumina). In addition, we recently established the Division of Clinical Cancer Genetics for personalized cancer medicine. We obtain biospecimens including blood and tissue fixed using the PAXgene Tissue system, and the samples are immediately analyzed for targeted amplicon sequencing using MiSeq. The rest of the samples are stored after adequate procedures in a -80 degree freezer. We obtain DNA and RNA from PAX-fixed paraffin- embedded samples with a high quality and sufficient amounts for clinical sequencing after pathological evalua- tion. For three months, we examined 40 cancer patients and performed targeted exome sequencing. As a result, detection rates of actionable and druggable gene mutations were around 85 and 50%, respectively. We have also established the Clinical Biobank Study Group in Japan, collaborating with several universities and cancer centers. We believe that this novel biospecimen repository system will help to effectively estab- lish cancer clinical sequencing throughout Japan.
基因组医学的发展使我们能够开展当代临床测序,而获取高质量生物样本并对这些材料进行妥善处理必不可少。我们于2014年启动了临床生物样本库,这是一种新型的按需存储系统。从2014年8月起的22个月里,我们存储了来自1700名患者的约6000份生物样本,其中大部分是为各种临床研究获取的。从PFPE样本中提取的DNA和RNA的质量和数量都非常高;因此,这些样本足以用于使用MiSeq(Illumina)进行靶向扩增子测序。此外,我们最近成立了临床癌症遗传学部门,用于个性化癌症医疗。我们获取包括血液和使用PAXgene Tissue系统固定的组织在内的生物样本,并立即对样本进行分析,以使用MiSeq进行靶向扩增子测序。其余样本经过适当处理后储存在-80℃的冰箱中。经过病理评估后,我们从PAX固定的石蜡包埋样本中获取了高质量且足够数量的DNA和RNA用于临床测序。在三个月的时间里,我们对40名癌症患者进行了检查并开展了靶向外显子组测序。结果,可操作和可用药基因突变的检测率分别约为85%和50%。我们还在日本成立了临床生物样本库研究小组,与几所大学和癌症中心开展合作。我们相信,这种新型生物样本库系统将有助于在日本各地有效建立癌症临床测序。