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


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
01 03 2021
Historique:
pubmed: 20 10 2020
medline: 31 3 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33074853
pii: 00000478-202103000-00011
doi: 10.1097/PAS.0000000000001601
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

394-404

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest and Source of Funding: The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article.

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Auteurs

Angela Chou (A)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.
NSW Health Pathology, Department of Anatomical Pathology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Mahsa Ahadi (M)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.
NSW Health Pathology, Department of Anatomical Pathology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Jennifer Arena (J)

Departments of Upper GI Surgery.

Loretta Sioson (L)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.

Amy Sheen (A)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.

Talia L Fuchs (TL)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.
NSW Health Pathology, Department of Anatomical Pathology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Nick Pavlakis (N)

Medical Oncology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Stephen Clarke (S)

Medical Oncology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Andrew Kneebone (A)

Radiation Oncology, Royal North Shore Hospital, St Leonards.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

George Hruby (G)

Radiation Oncology, Royal North Shore Hospital, St Leonards.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Sumit Sahni (S)

Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Anubhav Mittal (A)

Departments of Upper GI Surgery.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Jaswinder Samra (J)

Departments of Upper GI Surgery.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

Anthony J Gill (AJ)

Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research.
NSW Health Pathology, Department of Anatomical Pathology.
Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

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