Evidence map›Paper›PMID 41817932›Full record

ArticleAnnals of surgical oncology2026

Tissue Factor as a Prognostic and Therapeutic Biomarker in Resected Pancreatic Cancer.

Mariko Kamiya, Shiro Koizume, Tatsuya Kanai, Rei Kanemoto, Naohiko Matsushita, Shinnosuke Kawahara, Yuto Kamioka, Masaaki Murakawa, Kota Washimi, Satoshi Kobayashi and 7 more

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Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Mariko KamiyaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan. kamiyanwin@hotmail.co.jp.ORCID http://orcid.org/0000-0002-2867-423X
Shiro KoizumeMolecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Yokohama, Japan.
Tatsuya KanaiDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Rei KanemotoDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Naohiko MatsushitaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Shinnosuke KawaharaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Yuto KamiokaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Masaaki MurakawaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Kota WashimiDepartment of Pathology, Kanagawa Cancer Center, Yokohama, Japan.
Satoshi KobayashiDepartment of Gastroenterology, Hepatobiliary and Pancreatic Medical Oncology Division, Kanagawa Cancer Center, Yokohama, Japan.
Toru AoyamaDepartment of Surgery, Yokohama City University, Yokohama, Japan.
Makoto UenoDepartment of Gastroenterology, Hepatobiliary and Pancreatic Medical Oncology Division, Kanagawa Cancer Center, Yokohama, Japan.
Naoto YamamotoDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Takashi OshimaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Soichiro MorinagaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Aya SaitoDepartment of Surgery, Yokohama City University, Yokohama, Japan.
Yohei MiyagiMolecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Yokohama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTissue factor (TF), a key initiator of the coagulation cascade, is frequently overexpressed in pancreatic cancer and linked to tumor progression and thrombosis. While TF has been recognized as a prognostic biomarker, its clinical relevance in surgically treated patients remains unclear.

methodsWe retrospectively analyzed TF expression in resected pancreatic cancer specimens from 265 patients, including those with and without preoperative therapy, using immunohistochemistry. Tissue factor expression was semiquantitatively classified as negative, low, or high. Associations with clinicopathological features, treatment response, and survival were evaluated.

resultsHigh TF expression was observed in 17.4% of cases and was significantly associated with elevated CA19-9, biologically borderline resectable disease, and lymph node metastases. These patients had shorter overall survival (median overall survival: 20.6 vs. 38.8 vs. 53.6 months, p < 0.001). High TF expression remained an independent predictor of poor prognosis (hazard ratio [HR]: 2.21, p = 0.0002). Tissue factor-negative tumors were associated with favorable outcomes, including long-term survival despite recurrence. Tissue factor expression decreased following preoperative therapy but did not correlate with histological response.

conclusionsTissue factor expression stratifies pancreatic cancer into biologically and prognostically distinct subgroups. While high TF expression indicates aggressive disease and poor survival, TF-negative tumors represent an indolent, treatment-sensitive subtype. These findings underscore the biological heterogeneity of pancreatic cancer and support TF as a clinically relevant prognostic biomarker.

Indexed as

AdenocarcinomaBiomarkers, TumorNeoplasm Recurrence, LocalPancreatic NeoplasmsThromboplastinAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCA-19-9 AntigenFemaleFollow-Up StudiesHumansImmunoenzyme TechniquesLymphatic MetastasisMaleBiomarkers, TumorCA-19-9 AntigenThromboplastinImmunohistochemistryPancreatic cancerPreoperative therapyPrognostic biomarkerTissue factor

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.