Evidence map›Paper›PMID 27406244›Full record

ArticleFamilial cancer2017

Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer.

Isaura S Ibrahim, Bert A Bonsing, Rutger-Jan Swijnenburg, Lieke Welling, Roeland A Veenendaal, Martin N J M Wasser, Hans Morreau, Akin Inderson, Hans F A Vasen

Abstract readCase Reports
In one paragraph

Article in Familial cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

9 authors.

Isaura S IbrahimDepartment of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Bert A BonsingDepartment of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.
Rutger-Jan SwijnenburgDepartment of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.
Lieke WellingDepartment of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.
Roeland A VeenendaalDepartment of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Martin N J M WasserDepartment of Radiology, Leiden University Medical Centre, Leiden, The Netherlands.
Hans MorreauDepartment of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
Akin IndersonDepartment of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Hans F A VasenDepartment of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands. hfavasen@stoet.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 3-5 % of all cases of pancreatic ductal adenocarcinoma (PDAC), hereditary factors influence etiology. While surveillance of high-risk individuals may improve the prognosis, this study describes two very different outcomes in patients with screen-detected lesions. In 2000, a surveillance program of carriers of a CDKN2A/p16-Leiden-mutation consisting of annual MRI was initiated. Patients with a suspected pancreatic lesion undergo CT-scan and Endoscopic Ultrasound, and surgery is offered when a lesion is confirmed. In 2015, two patients with a screen-detected solid lesion were identified. In both patients, lesions were visible on MRI and CT scan, while the EUS was unremarkable. Surgical resection of the head of the pancreas resulted in nearly fatal complications in the first patient. This patient was shown to have a benign lesion. In contrast, timely identification of an early cancer in the second patient was accompanied by an uneventful postoperative course. These cases underline the risks inherent to a PDAC prevention program. All patients should be fully informed about the possible outcomes before joining a surveillance program.

Indexed as

Carcinoma, Pancreatic DuctalCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p18HeterozygoteHumansMagnetic Resonance ImagingMaleMiddle AgedPancreatic NeoplasmsTomography, X-Ray ComputedCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p18CDKN2A mutationComplicationsGenetic predispositionp16-Leiden mutationPancreatic ductal adenocarcinomaPDACPylorus-preserving pancreaticoduodenectomySurveillance

Identifiers

PMID27406244
PMCPMC5243878

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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.