Literature DB >> 27681847

Regression grading in neoadjuvant treated pancreatic cancer: an interobserver study.

Sangeetha N Kalimuthu1, Stefano Serra1, Neesha Dhani2, Sara Hafezi-Bakhtiari1, Eva Szentgyorgyi1, Rajkumar Vajpeyi1, Runjan Chetty1.   

Abstract

AIM: Several regression grading systems have been proposed for neoadjuvant chemoradiation-treated pancreatic ductal adenocarcinoma (PDAC). This study aimed to examine the utility, reproducibility and level of concordance of three most frequently used grading systems.
METHODS: Four gastrointestinal pathologists used the College of American Pathologists (CAP), Evans, MD Anderson Cancer Centre (MDA) regression grading systems to grade 14 selected cases (7-20 slides from each case) of neoadjuvant chemoradiation-treated PDAC. A postscoring discussion with each pathologist was conducted. The results were entered into a standardised data collection form and statistical analyses were performed.
RESULTS: There was little concordance across the three systems. The Kendall coefficient of concordance agreement scores were: CAP: 2-poor, 2-fair; Evans: 1-fair, 1-moderate, 2-good; MDA: 1-poor, 2-moderate, 1-good. Interpretation in all three grades in the CAP grading system was a source of discrepancy. Furthermore, using fibrosis as a criterion to assess regression was contentious. In the Evans system, quantifying tumour destruction using arbitrary percentage cut-offs (ie, 9% vs 10%; 50% vs 51%, etc) was imprecise and subjective. Although the MDA system generated greatest concordance, this was due to 'oversimplification' surrounding wide, arbitrarily assigned thresholds of </> 5% of tumour.
CONCLUSIONS: All systems lacked precision and clarity for accurate regression grading. Presently the clinical utility and impact of histological regression grading in patient management is questionable. There is a need to re-evaluate regression grading in the pancreas and establish a reproducible, clinically relevant grading system. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  CANCER; HISTOPATHOLOGY; NEOPLASMS; ONCOLOGY; PANCREATIC CANCER

Mesh:

Year:  2016        PMID: 27681847     DOI: 10.1136/jclinpath-2016-203947

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  13 in total

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8.  Area of residual tumor (ART) can predict prognosis after post neoadjuvant therapy resection for pancreatic ductal adenocarcinoma.

Authors:  Satoshi Okubo; Motohiro Kojima; Yoko Matsuda; Masayoshi Hioki; Yasuhiro Shimizu; Hirochika Toyama; Soichiro Morinaga; Naoto Gotohda; Katsuhiko Uesaka; Genichiro Ishii; Mari Mino-Kenudson; Shinichiro Takahashi
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