Kashiro Ayumi, Jung Giman, Honda Kazufumi
Institution for Advanced Medical Science, Nippon Medical School, Tokyo, Japan.
Bio-Tool Department, Toray International America, Inc., Brisbane, CA, USA.
Cancer Biomark. 2025 Mar;42(3):18758592251317405. doi: 10.1177/18758592251317405. Epub 2025 Apr 2.
Pancreatic cancer is a rare and refractory cancer, and the development of blood biomarkers for the enrichment of high-risk individuals who have risk factors for pancreatic cancer from the asymptomatic population is an unmet medical need. We identified abnormalities in the C-terminal truncation of the apolipoprotein A2 dimer (apoA2-isoforms: apoA2-i) in the blood of pancreatic cancer patients through proteomic analysis, and we have reported the potential for diagnosing resectable pancreatic cancer by detecting these abnormalities. We successfully developed enzyme-linked immunosorbent assay (ELISA) reagents for measuring apoA2-i for research use only, and then the basic data for diagnosing pancreatic cancer were accumulated by several studies using these reagents. In 2023, ELISA for measuring apoA2-i was regenerated by the regulation under the Japanese Quality Management System (QMS), it received marketing approval in Japan as an diagnostic (IVD) kit to aid in the diagnosis of pancreatic cancer, and it is now used in clinical practice. This review chronicles the journey from the initial discovery through omics research, to demonstrating clinical utility via multicenter studies in Japan and international collaborative research using the research reagent and validating the clinical performance of the IVD ELISA kit through a regulatory, science-guided, clinical trial in Japan, and finally to recent activities in the USA.
胰腺癌是一种罕见且难治的癌症,从无症状人群中筛选出具有胰腺癌危险因素的高危个体并开发相关血液生物标志物,是一项尚未满足的医学需求。我们通过蛋白质组学分析,在胰腺癌患者血液中发现了载脂蛋白A2二聚体(apoA2-异构体:apoA2-i)的C端截短异常,并报告了通过检测这些异常来诊断可切除胰腺癌的可能性。我们成功开发了仅用于研究的检测apoA2-i的酶联免疫吸附测定(ELISA)试剂,随后通过多项使用这些试剂的研究积累了诊断胰腺癌的基础数据。2023年,检测apoA2-i的ELISA试剂依据日本质量管理体系(QMS)的规定进行了更新,并作为诊断(IVD)试剂盒在日本获得上市批准,用于辅助胰腺癌的诊断,目前已应用于临床实践。这篇综述记录了从最初通过组学研究发现,到在日本通过多中心研究及国际合作研究利用研究试剂证明临床效用,并通过日本一项由监管机构指导、科学设计的临床试验验证IVD ELISA试剂盒的临床性能,直至近期在美国开展的相关活动的整个历程。