Evidence map›Paper›PMID 38451583›Full record

ArticleUnited European gastroenterology journal2024

Temporal progression of pancreatic cancer computed tomography findings until diagnosis: A large-scale multicenter study.

Masanori Gonda, Atsuhiro Masuda, Takashi Kobayashi, Takao Iemoto, Saori Kakuyama, Takeshi Ezaki, Takuya Ikegawa, Yuichi Hirata, Hidetaka Tsumura, Kyohei Ogisu and 17 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in United European gastroenterology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.4field-weighted citation impact, top 6% of its field
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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

27 authors at 16 institutions in 1 country.

Masanori GondaDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Atsuhiro MasudaDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.ORCID 0000-0002-2138-1207
Takashi KobayashiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Takao IemotoDepartment of Gastroenterology, Kitaharima Medical Center, Ono, Hyogo, Japan.
Saori KakuyamaDepartment of Gastroenterology, Takatsuki General Hospital, Takatsuki, Osaka, Japan.
Takeshi EzakiDepartment of Gastroenterology, National Hospital Organization Kobe Medical Center, Kobe, Hyogo, Japan.
Takuya IkegawaDepartment of Gastroenterology, Japanese Red Cross Kobe Hospital, Kobe, Hyogo, Japan.
Yuichi HirataDepartment of Gastroenterology, Kakogawa Central City Hospital, Kakogawa, Hyogo, Japan.
Hidetaka TsumuraDepartment of Gastroenterology, Hyogo Cancer Center, Akashi, Hyogo, Japan.
Kyohei OgisuDepartment of Gastroenterology, Nippon Life Hospital, Osaka, Osaka, Japan.
Ryota NakanoDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Seiji FujigakiDepartment of Gastroenterology, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji, Hyogo, Japan.
Takashi NakagawaDepartment of Gastroenterology, Chibune General Hospital, Osaka, Osaka, Japan.
Megumi TakagiDepartment of Gastroenterology, Osaka Saiseikai Nakatsu Hospital, Osaka, Osaka, Japan.
Kodai YamanakaDepartment of Gastroenterology, Konan Medical Center, Kobe, Hyogo, Japan.
Yu SatoDepartment of Internal Medicine, Hyogo Prefectural Tamba Medical Center, Tamba, Hyogo, Japan.
Koichi FujitaDepartment of Gastroenterology, Yodogawa Christian Hospital, Osaka, Osaka, Japan.ORCID 0000-0002-0768-1801
Keisuke FurumatsuDepartment of Gastroenterology, Akashi Medical Association Akashi Medical Center, Akashi, Hyogo, Japan.
Takao KatoDepartment of Gastroenterology, Hyogo Prefectural Awaji Medical Center, Sumoto, Hyogo, Japan.
Arata SakaiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Hideyuki ShiomiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Tsuyoshi SanukiDepartment of Gastroenterology, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji, Hyogo, Japan.
Yoshifumi ArisakaDepartment of Gastroenterology, Nippon Life Hospital, Osaka, Osaka, Japan.
Yoshihiro OkabeDepartment of Gastroenterology, Kakogawa Central City Hospital, Kakogawa, Hyogo, Japan.
Hirochika ToyamaDepartment of Hepato-Biliary-Pancreatic Surgery, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Keitaro SofueDepartment of Radiology, Kobe University Graduate School of Medicine and Kobe University Hospital, Kobe, Hyogo, Japan.
Yuzo KodamaDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Kobe University · JPHimeji Medical Center · JPHyogo Medical University · JPHyogo Prefectural Awaji Medical Center · JPKagawa Prefectural Central Hospital · JPOsaka Hospital · JPAkashi Medical Center · JPChibune General Hospital · JPHyogo Prefectural Cancer Center · JPJapanese Red Cross Kobe Hospital · JPKobe Medical Center · JPKobe University Hospital · JPSaiseikai Nakatsu Hospital · JPTakatsuki General Hospital · JPTokyo-Kita Medical Center · JPYodogawa Christian Hospital · JP

Funding

Japan Society for the Promotion of Science 19H03698Japan Society for the Promotion of Science 19K08444Japan Society for the Promotion of Science 22H03058Pancreas Research Foundation of Japan
6 · The paper itself

Abstract

backgroundFocal parenchymal atrophy and main pancreatic duct (MPD) dilatation have been identified as early signs of pancreatic ductal adenocarcinoma. However, limited evidence exists regarding their temporal progression due to previous study limitations with restricted case numbers.

objectiveTo ascertain a more precise frequency assessment of suspicious pancreatic ductal adenocarcinoma findings as well as delineate the temporal progression of them.

methodsA multicenter retrospective study was conducted on patients diagnosed with pancreatic ductal adenocarcinoma between 2015 and 2021. We included patients who had undergone at least one computed tomography (CT) scan ≥6 months before diagnosing pancreatic ductal adenocarcinoma. The temporal progression of suspicious pancreatic ductal adenocarcinoma findings on CT was investigated.

resultsOut of 1832 patients diagnosed with pancreatic ductal adenocarcinoma, 320 had a previous CT before their diagnosis. Suspicious pancreatic ductal adenocarcinoma findings were detected in 153 cases (47.8%), with focal parenchymal atrophy (26.6%) being the most common followed by MPD dilatation (11.3%). Focal parenchymal atrophy was the earliest detectable sign among all suspicious findings and became visible on average 2.7 years before diagnosis, and the next most common, MPD dilatation, 1.1 years before diagnosis. Other findings, such as retention cysts, were less frequent and appeared around 1 year before diagnosis. Focal parenchymal atrophy followed by MPD dilatation was observed in 10 patients but not in reverse order. Focal parenchymal atrophy was more frequently detected in the pancreatic body/tail. No significant relationship was found between the pathological pancreatic ductal adenocarcinoma differentiation or tumor stage and the time course of the CT findings. All cases of focal parenchymal atrophy progressed just prior to diagnosis, and the atrophic area was occupied by tumor at diagnosis. Main pancreatic duct dilatation continued to progress until diagnosis.

conclusionThis large-scale study revealed that the temporal progression of focal parenchymal atrophy is the earliest detectable sign indicating pancreatic ductal adenocarcinoma. These results provide crucial insights for early pancreatic ductal adenocarcinoma detection.

Indexed as

AtrophyCarcinoma, Pancreatic DuctalDisease ProgressionPancreatic DuctsPancreatic NeoplasmsTomography, X-Ray ComputedAdultAgedAged, 80 and overDilatation, PathologicEarly Detection of CancerFemaleHumansMaleMiddle AgedPancreascomputed tomographyearly diagnosisfocal parenchymal atrophymain pancreatic duct dilatationpancreatic cancerpancreatic ductal adenocarcinomapre‐diagnostic imagingretention cyststemporal progression

Identifiers

PMID38451583
PMCPMC11250140
OpenAlexW4392546611

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.