Evidence map›Paper›PMID 24111684›Full record

ArticleHistopathology2013

Pancreatic intraepithelial neoplasia and histological changes in non-neoplastic pancreas associated with neoadjuvant therapy in patients with pancreatic ductal adenocarcinoma.

Deyali Chatterjee, Matthew H Katz, Asif Rashid, Jeannelyn S Estrella, Hua Wang, Gauri R Varadhachary, Robert A Wolff, Jeffrey E Lee, Peter W Pisters, James L Abbruzzese and 2 more

Abstract read
In one paragraph

Article in Histopathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Defining post-operative pancreatitis as a new pancreatic specific complication following pancreatic resection.HPB : the official journal of the International Hepato Pancreato Biliary Association · 2016
    Pooled it
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Borderline resectable pancreatic cancer: Certainties and controversies.World journal of gastrointestinal surgery · 2021
    Review
  7. Article
  8. Early Detection in a Mouse Model of Pancreatic Cancer by Imaging DNA Damage Response Signaling.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2020
    Article
  9. Usefulness ofCancer medicine · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Pathologic assessment of gastrointestinal tract and pancreatic carcinoma after neoadjuvant therapy.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
    Review
  16. Article
  17. Article
  18. 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

12 authors.

Deyali ChatterjeeDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Matthew H Katz
Asif Rashid
Jeannelyn S Estrella
Hua Wang
Gauri R Varadhachary
Robert A Wolff
Jeffrey E Lee
Peter W Pisters
James L Abbruzzese
Jason B Fleming
Huamin Wang

Funding

Proteasome-mediated Degradation of Hematopoietic Progenitor Kinase 1 in PancreatiR21CA149544 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WANG, HUAMIN · 2011 to 2012
$378k
NCI NIH HHS 1R21CA149544-01A1NCI NIH HHS R21 CA149544
6 · The paper itself

Abstract

aimsTo study the histological changes in non-neoplastic pancreas and the effects on pancreatic intraepithelial neoplasia (PanIN) after neoadjuvant chemoradiation therapy (NCRT) for pancreatic ductal adenocarcinoma (PDAC). METHODS AND

resultsWe reviewed the archival H&E slides from 218 patients with PDAC who completed NCRT and pancreaticoduodenectomy. Sixty-five patients who underwent pancreaticoduodenectomy for PDAC without NCRT were used as controls. Various histological features were reviewed and correlated with NCRT and survival. The NCRT group had lower densities of PanIN2 (P = 0.004) and PanIN3 (P = 0.02) than the control group. The extent of fibrosis, the frequency of neuroma-like nerve proliferation and the frequency of islet cell aggregation were significantly higher in the NCRT group than in the control group (P < 0.05). The intensity of inflammation was less in the NCRT group than in the control group (P = 0.02). In the NCRT group, patents with moderate to severe fibrosis or grade 2 inflammation had poorer survival than those with mild fibrosis (P = 0.04) or those with grade 0 or grade 1 inflammation (P = 0.003), respectively.

conclusionsNon-neoplastic pancreatic tissue from patients who received NCRT had a reduced density of high-grade PanIN lesions, more pancreatic fibrosis, and higher frequencies of neuroma-like nerve proliferation and islet cell aggregation, but less inflammation, compared to tissue from those who did not receive NCRT.

Indexed as

Neoadjuvant TherapyAdultAgedAged, 80 and overCarcinoma in SituCarcinoma, Pancreatic DuctalCase-Control StudiesCell AggregationCell ProliferationFemaleFibrosisHumansInflammationIslets of LangerhansMaleMiddle Agedfibrosisinflammationislet cell aggregationneoadjuvant therapyneuroma-like nerve proliferationpancreatic cancerpancreatic intraepithelial neoplasia

Identifiers

PMID24111684
PMCPMC3836824

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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.