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Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)

An accurate and complete pathology report is critical for the optimal management of cutaneous melanoma patients. Protocols for the pathologic reporting of melanoma have been independently developed by the Royal College of Pathologists of Australasia (RCPA), Royal College of Pathologists (United King...

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Autores principales: Scolyer, Richard A., Judge, Meagan J., Evans, Alan, Frishberg, David P., Prieto, Victor G., Thompson, John F., Trotter, Martin J., Walsh, Maureen Y., Walsh, Noreen M.G., Ellis, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Raven Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864181/
https://www.ncbi.nlm.nih.gov/pubmed/24061524
http://dx.doi.org/10.1097/PAS.0b013e31829d7f35
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author Scolyer, Richard A.
Judge, Meagan J.
Evans, Alan
Frishberg, David P.
Prieto, Victor G.
Thompson, John F.
Trotter, Martin J.
Walsh, Maureen Y.
Walsh, Noreen M.G.
Ellis, David W.
author_facet Scolyer, Richard A.
Judge, Meagan J.
Evans, Alan
Frishberg, David P.
Prieto, Victor G.
Thompson, John F.
Trotter, Martin J.
Walsh, Maureen Y.
Walsh, Noreen M.G.
Ellis, David W.
author_sort Scolyer, Richard A.
collection PubMed
description An accurate and complete pathology report is critical for the optimal management of cutaneous melanoma patients. Protocols for the pathologic reporting of melanoma have been independently developed by the Royal College of Pathologists of Australasia (RCPA), Royal College of Pathologists (United Kingdom) (RCPath), and College of American Pathologists (CAP). In this study, data sets, checklists, and structured reporting protocols for pathologic examination and reporting of cutaneous melanoma were analyzed by an international panel of melanoma pathologists and clinicians with the aim of developing a common, internationally agreed upon, evidence-based data set. The International Collaboration on Cancer Reporting cutaneous melanoma expert review panel analyzed the existing RCPA, RCPath, and CAP data sets to develop a protocol containing “required” (mandatory/core) and “recommended” (nonmandatory/noncore) elements. Required elements were defined as those that had agreed evidentiary support at National Health and Medical Research Council level III-2 level of evidence or above and that were unanimously agreed upon by the review panel to be essential for the clinical management, staging, or assessment of the prognosis of melanoma or fundamental for pathologic diagnosis. Recommended elements were those considered to be clinically important and recommended for good practice but with lesser degrees of supportive evidence. Sixteen core/required data elements for cutaneous melanoma pathology reports were defined (with an additional 4 core/required elements for specimens received with lymph nodes). Eighteen additional data elements with a lesser level of evidentiary support were included in the recommended data set. Consensus response values (permitted responses) were formulated for each data item. Development and agreement of this evidence-based protocol at an international level was accomplished in a timely and efficient manner, and the processes described herein may facilitate the development of protocols for other tumor types. Widespread utilization of an internationally agreed upon, structured pathology data set for melanoma will lead not only to improved patient management but is a prerequisite for research and for international benchmarking in health care.
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spelling pubmed-38641812013-12-16 Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR) Scolyer, Richard A. Judge, Meagan J. Evans, Alan Frishberg, David P. Prieto, Victor G. Thompson, John F. Trotter, Martin J. Walsh, Maureen Y. Walsh, Noreen M.G. Ellis, David W. Am J Surg Pathol Original Articles An accurate and complete pathology report is critical for the optimal management of cutaneous melanoma patients. Protocols for the pathologic reporting of melanoma have been independently developed by the Royal College of Pathologists of Australasia (RCPA), Royal College of Pathologists (United Kingdom) (RCPath), and College of American Pathologists (CAP). In this study, data sets, checklists, and structured reporting protocols for pathologic examination and reporting of cutaneous melanoma were analyzed by an international panel of melanoma pathologists and clinicians with the aim of developing a common, internationally agreed upon, evidence-based data set. The International Collaboration on Cancer Reporting cutaneous melanoma expert review panel analyzed the existing RCPA, RCPath, and CAP data sets to develop a protocol containing “required” (mandatory/core) and “recommended” (nonmandatory/noncore) elements. Required elements were defined as those that had agreed evidentiary support at National Health and Medical Research Council level III-2 level of evidence or above and that were unanimously agreed upon by the review panel to be essential for the clinical management, staging, or assessment of the prognosis of melanoma or fundamental for pathologic diagnosis. Recommended elements were those considered to be clinically important and recommended for good practice but with lesser degrees of supportive evidence. Sixteen core/required data elements for cutaneous melanoma pathology reports were defined (with an additional 4 core/required elements for specimens received with lymph nodes). Eighteen additional data elements with a lesser level of evidentiary support were included in the recommended data set. Consensus response values (permitted responses) were formulated for each data item. Development and agreement of this evidence-based protocol at an international level was accomplished in a timely and efficient manner, and the processes described herein may facilitate the development of protocols for other tumor types. Widespread utilization of an internationally agreed upon, structured pathology data set for melanoma will lead not only to improved patient management but is a prerequisite for research and for international benchmarking in health care. Raven Press 2013-12 2013-11-26 /pmc/articles/PMC3864181/ /pubmed/24061524 http://dx.doi.org/10.1097/PAS.0b013e31829d7f35 Text en Copyright © 2013 by Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Original Articles
Scolyer, Richard A.
Judge, Meagan J.
Evans, Alan
Frishberg, David P.
Prieto, Victor G.
Thompson, John F.
Trotter, Martin J.
Walsh, Maureen Y.
Walsh, Noreen M.G.
Ellis, David W.
Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title_full Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title_fullStr Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title_full_unstemmed Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title_short Data Set for Pathology Reporting of Cutaneous Invasive Melanoma: Recommendations From the International Collaboration on Cancer Reporting (ICCR)
title_sort data set for pathology reporting of cutaneous invasive melanoma: recommendations from the international collaboration on cancer reporting (iccr)
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864181/
https://www.ncbi.nlm.nih.gov/pubmed/24061524
http://dx.doi.org/10.1097/PAS.0b013e31829d7f35
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