膵臓がんの早期発見につながる新たな血中バイオマーカーを特定 (Researchers Identify New Blood Markers That May Detect Early Pancreatic Cancer)

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20026-01-30 アメリカ国立衛生研究所(NIH)

米国国立衛生研究所(NIH)は、膵臓がんの早期発見につながる新たな血中バイオマーカーを特定したと発表した。膵臓がんは初期症状が乏しく、多くが進行期に診断されるため、死亡率が極めて高い。本研究では、膵臓がん患者の血液中に特徴的に現れる複数の分子を解析し、従来の指標よりも早期段階で高い検出精度を示す候補マーカー群を同定した。これらを既存の臨床指標と組み合わせることで、診断性能が大幅に向上する可能性が示された。研究者らは、将来的に簡便な血液検査として実用化されれば、ハイリスク群のスクリーニングや早期治療介入を可能にし、膵臓がんの予後改善に大きく貢献するとしている。

<関連情報>

アミノペプチダーゼN(ANPEP)とポリマー免疫グロブリン受容体(PIGR)を用いた膵管腺癌の早期発見のための血漿バイオマーカーパネルの改善 Improving a Plasma Biomarker Panel for Early Detection of Pancreatic Ductal Adenocarcinoma with Aminopeptidase N (ANPEP) and Polymeric Immunoglobulin Receptor (PIGR)

Brianna M. Krusen;Phyllis A. Gimotty;Greg Donahue;Jacob E. Till;Melinda Yin;Erin E. Carlson;William R. Bamlet;Erica L. Carpenter;Shounak Majumder;Ann L. Oberg;Kenneth S. Zaret
Clinical Cancer Research  Published:January 28 2026
DOI:https://doi.org/10.1158/1078-0432.CCR-25-3297

Abstract

Purpose:

Pancreatic ductal adenocarcinoma (PDAC) is typically detected too late for useful therapeutic interventions; hence, we sought blood biomarkers to detect early-stage disease.

Experimental Design:

Using mass spectrometry and ELISA on plasma pools from the University of Pennsylvania (Penn) and the Mayo Clinic (Mayo), we identified aminopeptidase N (ANPEP) and polymeric immunoglobulin receptor (PIGR) as increased in early-stage (stage I/II) PDAC plasma compared with controls. We tested ANPEP and PIGR, along with prior data for thrombospondin 2 (THBS2) and carbohydrate antigen 19-9 (CA19-9), in retrospective phase II studies using separate cohorts of PDAC plasmas at different stages versus healthy or nonmalignant disease controls (DC) from Penn (n = 135) and Mayo (n = 537).

Results:

Comparing healthy controls with stage I/II PDAC, we obtained area under the receiver-operating characteristic curves (AUC) of 0.78 [95% confidence interval (CI), 0.68–0.86]/0.80 (95% CI, 0.74–0.85; ANPEP) and 0.81 (95% CI, 0.70–0.88)/0.86 (95% CI, 0.82–0.90; PIGR) for the Penn/Mayo phase II studies, respectively. In multivariable models, CA19-9/THBS2/ANPEP, CA19-9/THBS2/PIGR, and CA19-9/THBS2/ANPEP/PIGR elicited AUC of 0.94 to 0.96 for Penn and 0.97 for Mayo. Notably, the four-marker panel elicited AUC of 0.87 for the Mayo stage I/II versus DC and 0.91 for stages I to IV versus DC. At a specificity of 95%, a plasma biomarker panel composed of CA19-9 (≥35 U/mL), THBS2 (≥42 ng/mL), ANPEP (≥2,995 ng/mL), and PIGR (≥1,800 ng/mL) yielded a sensitivity of 91.9% for PDAC stages I to IV and 87.5% for PDAC stage I/II.

Conclusions:

Adding ANPEP and PIGR to a plasma biomarker panel of CA19-9 and THBS2 enhances the detection of early-stage PDAC when comparing cancer versus healthy or nonmalignant DC. Given the concordance of our data in two retrospective phase II studies, assessments in prediagnostic cases are warranted.

医療・健康
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