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Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis
Immune checkpoint inhibitor-associated colitis (ICIC) affects approximately 15% of cancer patients treated with immunotherapy. Although histological evaluation is potentially valuable for both the diagnosis of ICIC and evaluation of disease activity, use in clinical practice is heterogeneous. We aim...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928359/ https://www.ncbi.nlm.nih.gov/pubmed/35296560 http://dx.doi.org/10.1136/jitc-2022-004560 |
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author | Ma, Christopher Pai, Rish K Schaeffer, David F Krell, Jonathan Guizzetti, Leonardo McFarlane, Stefanie C MacDonald, John K Choi, Won-Tak Feakins, Roger M Kirsch, Richard Lauwers, Gregory Y Pai, Reetesh K Rosty, Christophe Srivastava, Amitabh Walsh, Joanna C. Feagan, Brian G Jairath, Vipul |
author_facet | Ma, Christopher Pai, Rish K Schaeffer, David F Krell, Jonathan Guizzetti, Leonardo McFarlane, Stefanie C MacDonald, John K Choi, Won-Tak Feakins, Roger M Kirsch, Richard Lauwers, Gregory Y Pai, Reetesh K Rosty, Christophe Srivastava, Amitabh Walsh, Joanna C. Feagan, Brian G Jairath, Vipul |
author_sort | Ma, Christopher |
collection | PubMed |
description | Immune checkpoint inhibitor-associated colitis (ICIC) affects approximately 15% of cancer patients treated with immunotherapy. Although histological evaluation is potentially valuable for both the diagnosis of ICIC and evaluation of disease activity, use in clinical practice is heterogeneous. We aimed to develop expert recommendations to standardize histological assessment of disease activity in patients with ICIC. Using the modified Research and Development/University of California Los Angeles (RAND/UCLA) appropriateness methodology, an international panel of 11 pathologists rated the appropriateness of 99 statements on a 9-point Likert scale during two rounds of anonymous voting. Results were discussed between rounds using moderated videoconferences. There are currently no disease-specific instruments for assessing histological features of ICIC. The panel considered that colonoscopy with at least three biopsies per segment from a total of at least five segments, including both endoscopically normal and inflamed areas, was appropriate for tissue acquisition. They agreed that biopsies should be oriented such that the long axis of the colonic crypts is visualized and should be stained with hematoxylin and eosin. Histological items that the panel voted were appropriate to evaluate in ICIC included the degree of structural/architectural change, chronic inflammatory infiltrate, lamina propria and intraepithelial neutrophils, crypt abscesses and destruction, erosions/ulcerations, apoptosis, surface intraepithelial lymphocytosis, and subepithelial collagen thickness. The appropriateness of routine immunohistochemistry was uncertain. These expert recommendations will help standardize assessment of histological activity in patients with ICIC. The panel also identified the development and validation of an ICIC-specific histological index as a research priority. |
format | Online Article Text |
id | pubmed-8928359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-89283592022-04-01 Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis Ma, Christopher Pai, Rish K Schaeffer, David F Krell, Jonathan Guizzetti, Leonardo McFarlane, Stefanie C MacDonald, John K Choi, Won-Tak Feakins, Roger M Kirsch, Richard Lauwers, Gregory Y Pai, Reetesh K Rosty, Christophe Srivastava, Amitabh Walsh, Joanna C. Feagan, Brian G Jairath, Vipul J Immunother Cancer Position Article and Guidelines Immune checkpoint inhibitor-associated colitis (ICIC) affects approximately 15% of cancer patients treated with immunotherapy. Although histological evaluation is potentially valuable for both the diagnosis of ICIC and evaluation of disease activity, use in clinical practice is heterogeneous. We aimed to develop expert recommendations to standardize histological assessment of disease activity in patients with ICIC. Using the modified Research and Development/University of California Los Angeles (RAND/UCLA) appropriateness methodology, an international panel of 11 pathologists rated the appropriateness of 99 statements on a 9-point Likert scale during two rounds of anonymous voting. Results were discussed between rounds using moderated videoconferences. There are currently no disease-specific instruments for assessing histological features of ICIC. The panel considered that colonoscopy with at least three biopsies per segment from a total of at least five segments, including both endoscopically normal and inflamed areas, was appropriate for tissue acquisition. They agreed that biopsies should be oriented such that the long axis of the colonic crypts is visualized and should be stained with hematoxylin and eosin. Histological items that the panel voted were appropriate to evaluate in ICIC included the degree of structural/architectural change, chronic inflammatory infiltrate, lamina propria and intraepithelial neutrophils, crypt abscesses and destruction, erosions/ulcerations, apoptosis, surface intraepithelial lymphocytosis, and subepithelial collagen thickness. The appropriateness of routine immunohistochemistry was uncertain. These expert recommendations will help standardize assessment of histological activity in patients with ICIC. The panel also identified the development and validation of an ICIC-specific histological index as a research priority. BMJ Publishing Group 2022-03-16 /pmc/articles/PMC8928359/ /pubmed/35296560 http://dx.doi.org/10.1136/jitc-2022-004560 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Position Article and Guidelines Ma, Christopher Pai, Rish K Schaeffer, David F Krell, Jonathan Guizzetti, Leonardo McFarlane, Stefanie C MacDonald, John K Choi, Won-Tak Feakins, Roger M Kirsch, Richard Lauwers, Gregory Y Pai, Reetesh K Rosty, Christophe Srivastava, Amitabh Walsh, Joanna C. Feagan, Brian G Jairath, Vipul Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title | Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title_full | Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title_fullStr | Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title_full_unstemmed | Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title_short | Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
title_sort | recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis |
topic | Position Article and Guidelines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928359/ https://www.ncbi.nlm.nih.gov/pubmed/35296560 http://dx.doi.org/10.1136/jitc-2022-004560 |
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