Cargando…

Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study

Immunohistochemistry (IHC) and polymerase chain reaction (PCR) and fragment separation by capillary electrophoresis represent the current clinical laboratory standard for the evaluation of microsatellite instability (MSI) status. The importance of reporting MSI status in colorectal cancer is based o...

Descripción completa

Detalles Bibliográficos
Autores principales: Malapelle, Umberto, Parente, Paola, Pepe, Francesco, De Luca, Caterina, Cerino, Pellegrino, Covelli, Claudia, Balestrieri, Mariangela, Russo, Gianluca, Bonfitto, Antonio, Pisapia, Pasquale, Fiordelisi, Fabiola, D’Armiento, Maria, Bruzzese, Dario, Loupakis, Fotios, Pietrantonio, Filippo, Triassi, Maria, Fassan, Matteo, Troncone, Giancarlo, Graziano, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565496/
https://www.ncbi.nlm.nih.gov/pubmed/32887373
http://dx.doi.org/10.3390/cells9092019
_version_ 1783595945675456512
author Malapelle, Umberto
Parente, Paola
Pepe, Francesco
De Luca, Caterina
Cerino, Pellegrino
Covelli, Claudia
Balestrieri, Mariangela
Russo, Gianluca
Bonfitto, Antonio
Pisapia, Pasquale
Fiordelisi, Fabiola
D’Armiento, Maria
Bruzzese, Dario
Loupakis, Fotios
Pietrantonio, Filippo
Triassi, Maria
Fassan, Matteo
Troncone, Giancarlo
Graziano, Paolo
author_facet Malapelle, Umberto
Parente, Paola
Pepe, Francesco
De Luca, Caterina
Cerino, Pellegrino
Covelli, Claudia
Balestrieri, Mariangela
Russo, Gianluca
Bonfitto, Antonio
Pisapia, Pasquale
Fiordelisi, Fabiola
D’Armiento, Maria
Bruzzese, Dario
Loupakis, Fotios
Pietrantonio, Filippo
Triassi, Maria
Fassan, Matteo
Troncone, Giancarlo
Graziano, Paolo
author_sort Malapelle, Umberto
collection PubMed
description Immunohistochemistry (IHC) and polymerase chain reaction (PCR) and fragment separation by capillary electrophoresis represent the current clinical laboratory standard for the evaluation of microsatellite instability (MSI) status. The importance of reporting MSI status in colorectal cancer is based on its potential for guiding treatment and as a prognostic indicator. It is also used to identify patients for Lynch syndrome testing. Our aim was to evaluate pre-analytical factors, such as age of formalin-fixed and paraffin-embedded (FFPE) block, neoplastic cell percentage, mucinous component, and DNA integrity, that may influence the accuracy of MSI testing and assess the concordance between three different MSI evaluation approaches. We selected the mucinous colorectal cancer (CRC) histotype for this study as it may possibly represent an intrinsic diagnostic issue due to its low tumor cellularity. Seventy-five cases of mucinous CRC and corresponding normal colon tissue samples were retrospectively selected. MMR proteins were evaluated by IHC. After DNA quality and quantity evaluation, the Idylla™ and TapeStation 4200 platforms were adopted for the evaluation of MSI status. Seventy-three (97.3%) cases were successfully analyzed by the three methodologies. Overall, the Idylla™ platform showed a concordance rate with IHC of 98.0% for microsatellite stable (MSS)/proficient MMR (pMMR) cases and 81.8% for MSI/deficient MMR (dMMR) cases. The TapeStation 4200 system showed a concordance rate with IHC of 96.0% for MSS/pMMR cases and 45.4% for MSI/dMMR cases. The concordance rates of the TapeStation 4200 system with respect to the Idylla™ platform were 98.1% for MSS profile and 57.8% for MSI profile. Discordant cases were analyzed using the Titano MSI kit. Considering pre-analytical factors, no significant variation in concordance rate among IHC analyses and molecular systems was observed by considering the presence of an acellular mucus cut-off >50% of the tumor area, FFPE year preparation, and DNA concentration. Conversely, the Idylla™ platform showed a significant variation in concordance rate with the IHC approach by considering a neoplastic cell percentage >50% (p-value = 0.002), and the TapeStation 4200 system showed a significant variation in concordance rate with the IHC approach by considering a DNA integrity number (DIN) ≥4 as cut-off (p-value = 0.009). Our data pinpoint a central role of the pre-analytical phase in the diagnostic outcome of MSI testing in CRC.
format Online
Article
Text
id pubmed-7565496
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-75654962020-10-26 Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study Malapelle, Umberto Parente, Paola Pepe, Francesco De Luca, Caterina Cerino, Pellegrino Covelli, Claudia Balestrieri, Mariangela Russo, Gianluca Bonfitto, Antonio Pisapia, Pasquale Fiordelisi, Fabiola D’Armiento, Maria Bruzzese, Dario Loupakis, Fotios Pietrantonio, Filippo Triassi, Maria Fassan, Matteo Troncone, Giancarlo Graziano, Paolo Cells Article Immunohistochemistry (IHC) and polymerase chain reaction (PCR) and fragment separation by capillary electrophoresis represent the current clinical laboratory standard for the evaluation of microsatellite instability (MSI) status. The importance of reporting MSI status in colorectal cancer is based on its potential for guiding treatment and as a prognostic indicator. It is also used to identify patients for Lynch syndrome testing. Our aim was to evaluate pre-analytical factors, such as age of formalin-fixed and paraffin-embedded (FFPE) block, neoplastic cell percentage, mucinous component, and DNA integrity, that may influence the accuracy of MSI testing and assess the concordance between three different MSI evaluation approaches. We selected the mucinous colorectal cancer (CRC) histotype for this study as it may possibly represent an intrinsic diagnostic issue due to its low tumor cellularity. Seventy-five cases of mucinous CRC and corresponding normal colon tissue samples were retrospectively selected. MMR proteins were evaluated by IHC. After DNA quality and quantity evaluation, the Idylla™ and TapeStation 4200 platforms were adopted for the evaluation of MSI status. Seventy-three (97.3%) cases were successfully analyzed by the three methodologies. Overall, the Idylla™ platform showed a concordance rate with IHC of 98.0% for microsatellite stable (MSS)/proficient MMR (pMMR) cases and 81.8% for MSI/deficient MMR (dMMR) cases. The TapeStation 4200 system showed a concordance rate with IHC of 96.0% for MSS/pMMR cases and 45.4% for MSI/dMMR cases. The concordance rates of the TapeStation 4200 system with respect to the Idylla™ platform were 98.1% for MSS profile and 57.8% for MSI profile. Discordant cases were analyzed using the Titano MSI kit. Considering pre-analytical factors, no significant variation in concordance rate among IHC analyses and molecular systems was observed by considering the presence of an acellular mucus cut-off >50% of the tumor area, FFPE year preparation, and DNA concentration. Conversely, the Idylla™ platform showed a significant variation in concordance rate with the IHC approach by considering a neoplastic cell percentage >50% (p-value = 0.002), and the TapeStation 4200 system showed a significant variation in concordance rate with the IHC approach by considering a DNA integrity number (DIN) ≥4 as cut-off (p-value = 0.009). Our data pinpoint a central role of the pre-analytical phase in the diagnostic outcome of MSI testing in CRC. MDPI 2020-09-02 /pmc/articles/PMC7565496/ /pubmed/32887373 http://dx.doi.org/10.3390/cells9092019 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Malapelle, Umberto
Parente, Paola
Pepe, Francesco
De Luca, Caterina
Cerino, Pellegrino
Covelli, Claudia
Balestrieri, Mariangela
Russo, Gianluca
Bonfitto, Antonio
Pisapia, Pasquale
Fiordelisi, Fabiola
D’Armiento, Maria
Bruzzese, Dario
Loupakis, Fotios
Pietrantonio, Filippo
Triassi, Maria
Fassan, Matteo
Troncone, Giancarlo
Graziano, Paolo
Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title_full Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title_fullStr Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title_full_unstemmed Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title_short Impact of Pre-Analytical Factors on MSI Test Accuracy in Mucinous Colorectal Adenocarcinoma: A Multi-Assay Concordance Study
title_sort impact of pre-analytical factors on msi test accuracy in mucinous colorectal adenocarcinoma: a multi-assay concordance study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565496/
https://www.ncbi.nlm.nih.gov/pubmed/32887373
http://dx.doi.org/10.3390/cells9092019
work_keys_str_mv AT malapelleumberto impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT parentepaola impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT pepefrancesco impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT delucacaterina impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT cerinopellegrino impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT covelliclaudia impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT balestrierimariangela impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT russogianluca impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT bonfittoantonio impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT pisapiapasquale impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT fiordelisifabiola impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT darmientomaria impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT bruzzesedario impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT loupakisfotios impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT pietrantoniofilippo impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT triassimaria impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT fassanmatteo impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT tronconegiancarlo impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy
AT grazianopaolo impactofpreanalyticalfactorsonmsitestaccuracyinmucinouscolorectaladenocarcinomaamultiassayconcordancestudy