Evidence map›Paper›PMID 40890542›Full record

ArticleAnnals of surgical oncology2025

Favorable Response Defined by CA19-9 Reduction After Neoadjuvant Treatment for Pancreatic Cancer.

Yuya Ashitomi, Fuyuhiko Motoi, Atsushi Oba, Teiichi Sugiura, Daisuke Hashimoto, Koetsu Inoue, Kenjiro Okada, Hideki Takami, Toru Nakamura, Ryosuke Takahashi and 12 more

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Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Yuya AshitomiDepartment of Surgery I, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Fuyuhiko MotoiDepartment of Surgery I, Faculty of Medicine, Yamagata University, Yamagata, Japan. fmotoi@med.id.yamagata-u.ac.jp.ORCID http://orcid.org/0000-0001-7601-8395
Atsushi ObaDivision of Hepato-Biliary-Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Teiichi SugiuraDepartment of Hepato-Biliary-Pancreatic Surgery, Shizuoka Cancer Center, Nagaizumi, Japan.
Daisuke HashimotoDepartment of Pancreatobiliary Surgery, Kansai Medical University, Hirakata, Japan.
Koetsu InoueDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kenjiro OkadaDepartment of Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Higashihiroshima, Japan.
Hideki TakamiDepartment of Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Toru NakamuraDepartment of Gastroenterological Surgery II, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Ryosuke TakahashiDepartment of Surgery I, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Keiichi AkahoshiDepartment of Hepatobiliary and Pancreatic Surgery, Tokyo Medical and Dental University, Bunkyō, Japan.
Kimitaka TanakaDepartment of Gastroenterological Surgery II, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Hideki IshikawaDepartment of Molecular-Targeting Prevention, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kojiro OmiyaDivision of Hepato-Biliary-Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Katsuhisa OhgiDepartment of Hepato-Biliary-Pancreatic Surgery, Shizuoka Cancer Center, Nagaizumi, Japan.
So YamakiDepartment of Pancreatobiliary Surgery, Kansai Medical University, Hirakata, Japan.
Masamichi MizumaDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kenichiro UemuraDepartment of Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Higashihiroshima, Japan.
Shuichiro SugawaraDepartment of Surgery I, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Satoshi HiranoDepartment of Gastroenterological Surgery II, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Sohei SatoiDepartment of Pancreatobiliary Surgery, Kansai Medical University, Hirakata, Japan.
Hepato-pancreato-biliary Scientific Network for clinical Oncology research Working (HPB SNOW)

Funding

Japan Society for the Promotion of Science Grant-in-Aid for Scientific Research (C) 23K08125
6 · The paper itself

Abstract

backgroundNeoadjuvant treatment (NAT) for pancreatic cancer has been shown to reduce mortality risk, with carbohydrate antigen (CA)19-9 response indicating survival outcomes. The purpose of this study is to clarify the degree of the CA19-9 response after neoadjuvant treatment (NAT) on prognosis. PATIENTS AND

methodsIn this retrospective, multicenter, observational study involving 1811 patients with pancreatic cancer scheduled for surgery, patients were stratified on the basis of pretreatment CA19-9 levels into elevated CA19-9 level and CA19-9 within the normal range groups. The groups were further divided into upfront surgery (UPS) and NAT subgroups.

resultsPatients with high CA19-9 levels had significantly poorer prognoses compared with those with normal levels. Among the high CA19-9 group, patients undergoing NAT demonstrated significantly improved prognoses compared with those receiving UPS. Further analysis of the high CA19-9 and received NAT group stratified by CA19-9 response showed clearly different median survivals: normalized CA19-9 group > decreased but not normalized CA19-9 group > increased CA19-9 after NAT group. Notably, patients with post-NAT CA19-9 levels < 296 U/mL (eightfold of upper limit) and > 40% reduction in CA19-9 levels had equivalent prognoses as those with normalized CA19-9 levels, while those with post-NAT CA19-9 levels > 296 U/mL and/or < 40% reduction in its value had a worse prognosis, akin to those with increased CA19-9 after NAT.

conclusionsNAT improves the prognosis of patients with pancreatic cancer with high CA19-9 levels, allowing for clear stratification of patients into favorable responders, defined as those with post-NAT normalized CA19-9 or levels < 296 U/mL with a > 40% reduction in CA19-9, and unfavorable responders.

Indexed as

CA19-9Neoadjuvant therapyPancreatic cancerPrognosisSurgery

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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.