Literature DB >> 33074853

A Critical Assessment of Postneoadjuvant Therapy Pancreatic Cancer Regression Grading Schemes With a Proposal for a Novel Approach.

Angela Chou1,2,3, Mahsa Ahadi1,2,3, Jennifer Arena4, Loretta Sioson1, Amy Sheen1, Talia L Fuchs1,2,3, Nick Pavlakis5,3, Stephen Clarke5,3, Andrew Kneebone6,3, George Hruby6,3, Sumit Sahni3, Anubhav Mittal4,3, Jaswinder Samra4,3, Anthony J Gill1,2,3.   

Abstract

Currently, there is no consensus on the optimal tumor response score (TRS) system to assess regression in pancreatic cancers resected after neoadjuvant therapy. We developed a novel TRS (Royal North Shore [RNS] system) based on estimating the percentage of tumor bed occupied by viable cancer and categorized into 3 tiers: grade 1 (≤10%), grade 2 (11% to 75%), and grade 3 (>75%). We assessed 147 resected carcinomas with this and other TRS systems (College of American Pathologists [CAP], MD Anderson Cancer Center [MDACC], and Evans). The 3-tiered RNS system predicted median survival after surgery for grades 1, 2, and 3 of 54, 23, and 9 months, respectively (P<0.05). The CAP, MDACC, and Evans systems also predicted survival (P<0.05) but less consistently. The median survival for MDACC and CAP grade 0 (complete regression) was less than MDACC grade 1 and CAP grades 1 and 2. There was no difference in survival between CAP grades 2 and 3 (P=0.960), Evans grades 1 and 2a (P=0.395), and Evans grades 2a and 2b (P=0.587). Interobserver concordance was weak for CAP (κ=0.431), moderate for MDACC (κ=0.691), minimal for Evans (κ=0.307), and moderate to strong for RNS (κ=0.632 to 0.84). Of age, sex, size, stage, grade, perineural and vascular invasion, extrapancreatic extension, margin status, and RNS score, only RNS score, vascular invasion, and extrapancreatic extension predicted survival in univariate analysis. Only extrapancreatic extension (P=0.034) and RNS score (P<0.0001) remained significant in multivariate analysis. We conclude that the RNS system is a reproducible and powerful predictor of survival after resection for pancreatic cancers treated with neoadjuvant therapy and should be investigated in larger cohorts.
Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Entities:  

Year:  2021        PMID: 33074853     DOI: 10.1097/PAS.0000000000001601

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  4 in total

Review 1.  Critical issues in pathologic evaluation of pancreatic ductal adenocarcinoma resected after neoadjuvant treatment: a narrative review.

Authors:  Mehran Taherian; Huamin Wang
Journal:  Chin Clin Oncol       Date:  2022-06-16

2.  Pathologic Examination of Pancreatic Specimens Resected for Treated Pancreatic Ductal Adenocarcinoma: Recommendations From the Pancreatobiliary Pathology Society.

Authors:  Huamin Wang; Runjan Chetty; Mojgan Hosseini; Daniela S Allende; Irene Esposito; Yoko Matsuda; Vikram Deshpande; Jiaqi Shi; Deepti Dhall; Kee-Taek Jang; Grace E Kim; Claudio Luchini; Rondell P Graham; Michelle D Reid; Olca Basturk; Ralph H Hruban; Alyssa Krasinskas; David S Klimstra; Volkan Adsay
Journal:  Am J Surg Pathol       Date:  2021-12-15       Impact factor: 6.298

3.  Stroma composition and proliferative activity are related to therapy response in neoadjuvant treated pancreatic ductal adenocarcinoma.

Authors:  Lena Haeberle; Andrea Cacciato Insilla; Anne-Christine Kapp; Katja Steiger; Anna Melissa Schlitter; Björn Konukiewitz; Ihsan Ekin Demir; Helmut Friess; Irene Esposito
Journal:  Histol Histopathol       Date:  2021-03-26       Impact factor: 2.303

Review 4.  Pancreatic Ductal Adenocarcinoma: Molecular Pathology and Predictive Biomarkers.

Authors:  Mehran Taherian; Hua Wang; Huamin Wang
Journal:  Cells       Date:  2022-09-29       Impact factor: 7.666

  4 in total

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