
Researchers at Kanazawa University report that blood-based gene expression tests may enable early pancreatic cancer screening and improve long-term survival.
Pancreatic cancer is one of the most malignant cancers, with a five-year relative survival rate of only 8.5% in Japan (2009–2011, National Cancer Center data). Curative treatment is possible only when the disease is detected early and surgical resection can be performed. However, early-stage pancreatic cancer accounts for only 2–3% of all diagnosed cases because of the difficulty of early detection. This diagnostic challenge is a major factor contributing to the poor prognosis of pancreatic cancer. To improve outcomes, there is an urgent need for noninvasive diagnostic methods, particularly blood-based biomarkers, capable of efficiently detecting early-stage disease.
A research group led by Dr. Yamashita, dean of the Graduate School of Advanced Preventive Medical Sciences and professor of gastroenterology at the Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, previously developed a pancreatic cancer diagnostic test called “Panregza,” which combines gene expression patterns from peripheral whole blood with the serum tumor marker CA19-9. While its effectiveness has been demonstrated primarily in advanced pancreatic cancer, its usefulness for detecting early-stage disease had not been clarified until now.
Yamashita and colleagues analyzed 10 patients with stage 0–I pancreatic cancer (representing 4% of 253 cases) and compared them with 104 healthy individuals. The following diagnostic approaches were evaluated: 1. Peripheral whole blood gene expression patterns (mRNA); 2. Tumor marker CA19-9; and 3. Combined test.

Gene signals outperformed CA19-9
Using a panel of 56 gene probes, the gene expression approach successfully detected 9 of 10 cases (90%) of early-stage pancreatic cancer. In contrast, CA19-9 detected only 1 of 10 cases (10%), showing a substantial difference in detection performance. The combined Panregza test demonstrated 60% sensitivity and 93.3% specificity. These findings indicate that gene expression analysis from peripheral whole blood is a highly effective method for detecting early-stage pancreatic cancer.
At the Innovative Research and Development Center for Pancreatic Cancer at Kanazawa University Hospital, five-year survival rates are 100% for stage 0 and 74.4% for stage I pancreatic cancer, emphasizing the critical role of early diagnosis in improving prognosis.
Early-stage changes appear in blood
Researchers at Kanazawa University previously found that gene expression patterns in peripheral blood mononuclear cells (PBMCs) differ between patients with pancreatic cancer and healthy individuals. Based on this finding, they developed a diagnostic kit called Panregza using whole blood and CA19-9, which is currently marketed by Cubix Inc.
Most PBMCs are immune cells, and it has been assumed that pancreatic cancer cells induce changes in gene expression by influencing these immune cells. However, it has remained unclear whether such expression changes also occur in early-stage pancreatic cancer, where the tumor burden is minimal.
This study demonstrated that even in stage 0–I pancreatic cancer with normal CA19-9 levels, abnormalities in whole blood gene expression can be detected. These findings suggest that this diagnostic test enables early detection of pancreatic cancer and is not dependent on tumor volume.
Publication details
Masaki Miyazawa et al, Pilot validation of a whole-blood mRNA expression-based diagnostic system for early-stage pancreatic ductal adenocarcinoma: a single-center case–control diagnostic accuracy study, Scientific Reports (2026). DOI: 10.1038/s41598-026-58684-8
Journal information:
Scientific Reports
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