Evidence map›Paper›PMID 35229208›Full record

ArticleDigestive diseases and sciences2022

Serial EUS-Guided FNA for the Surveillance of Pancreatic Cysts: A Study of Long-Term Performance of Tumor Markers.

Mahmoud A Rahal, John M DeWitt, Harsh Patel, C Max Schmidt, Eugene P Ceppa, Rachel E Simpson, Stuart Sherman, Mohammad Al-Haddad

Abstract read
In one paragraph

Article in Digestive diseases and sciences, 2022. 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

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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

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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. Article
  2. Modern aspects of the management of pancreatic intraductal papillary mucinous neoplasms: a narrative review.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Review
4 · The record

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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

8 authors.

Mahmoud A RahalDepartment of Internal Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
John M DeWittDivision of Gastroenterology and Hepatology, Indiana University School of Medicine, 550 University Blvd, Suite 4100, Indianapolis, IN, 46202, USA.
Harsh PatelDepartment of Internal Medicine, Ochsner Clinic Foundation, New Orleans, LA, USA.
C Max SchmidtDepartment of Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.
Eugene P CeppaDepartment of Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.
Rachel E SimpsonDepartment of Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.
Stuart ShermanDivision of Gastroenterology and Hepatology, Indiana University School of Medicine, 550 University Blvd, Suite 4100, Indianapolis, IN, 46202, USA.
Mohammad Al-HaddadDivision of Gastroenterology and Hepatology, Indiana University School of Medicine, 550 University Blvd, Suite 4100, Indianapolis, IN, 46202, USA. moalhadd@iu.edu.ORCID 0000-0003-1641-9976

Funding

Indiana University (IU) Clinical Center for Chronic Pancreatitis Clinical Research NetworkU01DK108323 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Jeffrey James Easler, Evan L Fogel · 2015 to 2026
$6.5M
NIDDK NIH HHS U01 DK108323
6 · The paper itself

Abstract

BACKGROUND AND

aimThe natural history of KRAS mutations in mucinous pancreatic cysts (MPCs) over time remains to be fully understood. The aim of this study was to examine the performance of DNA markers and assess changes of KRAS mutations over time.

methodsPatients who underwent EUS-FNA of pancreatic cysts with at least two separate molecular analysis results were included in the study. We assessed the baseline patient and cyst characteristics, and DNA fluid analysis. The presence of either a KRAS mutation, or a CEA > 192 ng/ml was used as the diagnostic standard for mucinous cysts when surgical pathology was not available.

resultsA total of 933 pancreatic cyst fluid samples were collected, including 117 with ≥ 2 FNAs. Examinations were performed over a median of 30 months (range 1-115 months). Forty-three (36%) had a mutant KRAS on the index analysis out of which 26 had a change in their KRAS status to the wild-type. Eighty-one (64%) had a wild-type KRAS on the index analysis out of which 18 had change in their KRAS status to mutant type. There was no significant difference in the index cyst characteristics, presence of symptoms, or main duct involvement based on KRAS status change. Increasing age was associated with a changing KRAS mutation status (p = 0.023).

conclusionKRAS mutations gain and loss in pancreatic cyst fluid appears to occur frequently during long-term surveillance of MPCs. Age appears to be the only predictor for KRAS change over time.

Indexed as

Pancreatic CystPancreatic NeoplasmsBiomarkers, TumorCarcinoembryonic AntigenCyst FluidDNAEndoscopic Ultrasound-Guided Fine Needle AspirationGenetic MarkersHumansProto-Oncogene Proteins p21(ras)Biomarkers, TumorCarcinoembryonic AntigenDNAGenetic MarkersProto-Oncogene Proteins p21(ras)CEA (Carcinoembryonic Antigen)EUS-FNAIPMN (Intraductal Papillary Mucinous Neoplasm)KRAS

Identifiers

PMID35229208
PMCPMC10153767

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