Evidence map›Paper›PMID 42678419›Full record

ArticleVirchows Archiv : an international journal of pathology2026

Pancreatic ductal adenocarcinomas arising from intraductal papillary mucinous neoplasms are aggressive despite being low stage: implications on screening and "early diagnosis".

Burcin Pehlivanoglu, Takashi Muraki, Michelle D Reid, Bahar Memis, Serdar Balci, Pelin Bagci, Kadriye Ebru Akar, Juan Sarmiento, David Kooby, Shishir K Maithel and 4 more

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Article in Virchows Archiv : an international journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Burcin PehlivanogluDepartment of Pathology, Emory University School of Medicine, Atlanta, GA, USA.
Takashi MurakiDepartment of Pathology, Emory University School of Medicine, Atlanta, GA, USA.
Michelle D ReidDepartment of Pathology, Emory University School of Medicine, Atlanta, GA, USA.
Bahar MemisDepartment of Pathology, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey.
Serdar BalciDepartment of Pathology, Memorial Hospital, Istanbul, Turkey.
Pelin BagciBotton-Champalimaud Pancreatic Cancer Center, Lisbon, Portugal.
Kadriye Ebru AkarDepartment of Pathology, Marmara University School of Medicine, İstanbul, Turkey.
Juan SarmientoDepartment of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
David KoobyDepartment of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
Shishir K MaithelDepartment of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Susan TsaiDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
Kathleen ChristiansDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
Douglas B EvansDepartment of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
Volkan AdsayDepartment of Pathology, Koç University Hospital, Davutpaşa Caddesi No:4, Istanbul, Topkapi, 34010, Turkey. vadsay@kuh.ku.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The literature is highly conflicting regarding the nature and behavior of pancreatic ductal adenocarcinomas (PDAC) arising from intraductal papillary mucinous neoplasm (IPMN). We investigated and contrasted the clinicopathological features of PDACs associated with IPMN (I-PDAC, n = 52 - only bona-fide and ≥ 1 cm IPMNs along with ordinary pancreatobiliary type invasive adenocarcinomas were included in this group-), versus without (NI-PDAC, n = 390) versus those associated with other IPMN mimicker cysts (pseudo-IPMN-associated, ps-PDAC, n = 39) including retention cysts. In I-PDAC, the average size of the IPMN was 4.05 cm, and 36.5% were > 3 cm, and the PDAC components were captured at an earlier stage (49% pT1) as compared to NI-PDACs (21% pT1), and ps-PDACs (18% pT1). I-PDAC also had a lesser frequency of lymphovascular invasion and lymph node metastasis. However, despite being less advanced PDACs, the overall survival of patients with I-PDACs was only modestly superior to NI-PDACs and ps-PDACs without statistical significance (median survival 44.2 vs. 26.7 vs. 28.4 months, and 5-year survival 41.4% vs. 24% and 0%), and this gap further closed when PDAC size was matched. This data underscores: (1) In > 60% of I-PDACs, the IPMN component is < 3 cm. (2) Contradictory to the prevailing impression in the literature, conventional PDACs arising from frank IPMNs do not behave that much better than ordinary PDACs despite being less advanced. (3) Even small PDACs may warrant adjuvant treatment. (4) Additional studies are needed to preoperatively distinguish "trivial cysts" from progression-prone IPMNs. 4) Following surgical resection of PDAC, it is still important to distinguish the nature of a cyst ≥ 1 cm as IPMN vs. pseudo-IPMN as ps-PDACs are significantly more aggressive which may be related to their ability to cause secondary cystic changes which requires further scrutiny. (5) Screening and removing IPMNs before they become invasive is crucial. 5) Even "early" may be too late: Even I-PDACs that are early stage are lethal which may necessitate re-focusing research efforts on biology, and etiopathogenesis such as anatomy associated chemical carcinogenetic factors.

Indexed as

Intraductal papillary mucinous neoplasmIPMNPancreatic ductal adenocarcinomaPseudo-IPMNSurvival

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.