Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal

Detalhes bibliográficos
Autor(a) principal: Brito, María José
Data de Publicação: 2018
Outros Autores: Honavar, Mrinalini, Cipriano, Maria Augusta, Lopes, Joanne, Coelho, Helder, Silva, António Rodrigues da, Silva, Mário, Guimarães, Susana, Frutuoso, Amaro, Gomes, Ana, Barbosa, Elisabete, Carlos, Sandra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696
Resumo: Introduction: Approximately 20% - 30% of histological lymph node-negative patients with colorectal cancer relapse at five years after surgical treatment. This recurrence is likely due to occult nodal disease undetected by standard histopathological practice which has implications in terms of the clinical management of patients.Material and Methods: Lymph nodes were collected from colectomy specimens. A central section from each lymph node was histologically examined following haematoxylin-eosin staining and the remaining tissue was subjected to OSNA - one step nucleic acid amplification analysis.Results: A total of 1046 lymph nodes from 59 pN0 patients were assessed. Of these, 753 lymph nodes were examined by both methods. The median number of lymph nodes assessed with OSNA - one step nucleic acid amplification was 12 (IQR: 7;16). Among pN0 patients, 17 had OSNA - one step nucleic acid amplification-positive lymph nodes, resulting in a positive molecular staging rate of 28.8% (95% CI: 17.8 - 42.1). Among these patients, 12 (70.59%) were molecular-staged as pN1 and 5 (29.41%) were molecular staged as pN2. The tumour burden of lymph nodes assessed with OSNA - one step nucleic acid amplification ranged from 270 to 17 000 cytokeratin 19 mRNA copies/μL. Most of these patients (88.2%) were found to have lymph nodes with micrometastases only (250 - 4999 copies/μL).Discussion: We provide the results from the first study of the use of the OSNA - one step nucleic acid amplification assay in colorectal cancer patients in Portugal. Our results are in-line with other international studies, showing the improvement on patients’ staging by molecular examination of lymph nodes.Conclusion: In our study, 28.8% of patients with histologically negative lymph nodes were found to have metastatic lymph nodes using OSNA - one step nucleic acid molecular assessment. OSNA - one step nucleic acid assay allows a more accurate staging of patients with colorectal cancer and standardizes lymph node assessment.
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spelling Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in PortugalEstadiamento Molecular de Doentes com Carcinoma do Colon. O Estudo C-Closer-II: Um Estudo Multicêntrico em PortugalColorectal NeoplasmsLymph NodesLymphatic MetastasisNeoplasm StagingNucleic Acid Amplification TechniquesEstadiamento de NeoplasiasGânglios LinfáticosMetástase LinfáticaNeoplasias Colo-rectaisTécnicas de Amplificação de Ácido NucleicoIntroduction: Approximately 20% - 30% of histological lymph node-negative patients with colorectal cancer relapse at five years after surgical treatment. This recurrence is likely due to occult nodal disease undetected by standard histopathological practice which has implications in terms of the clinical management of patients.Material and Methods: Lymph nodes were collected from colectomy specimens. A central section from each lymph node was histologically examined following haematoxylin-eosin staining and the remaining tissue was subjected to OSNA - one step nucleic acid amplification analysis.Results: A total of 1046 lymph nodes from 59 pN0 patients were assessed. Of these, 753 lymph nodes were examined by both methods. The median number of lymph nodes assessed with OSNA - one step nucleic acid amplification was 12 (IQR: 7;16). Among pN0 patients, 17 had OSNA - one step nucleic acid amplification-positive lymph nodes, resulting in a positive molecular staging rate of 28.8% (95% CI: 17.8 - 42.1). Among these patients, 12 (70.59%) were molecular-staged as pN1 and 5 (29.41%) were molecular staged as pN2. The tumour burden of lymph nodes assessed with OSNA - one step nucleic acid amplification ranged from 270 to 17 000 cytokeratin 19 mRNA copies/μL. Most of these patients (88.2%) were found to have lymph nodes with micrometastases only (250 - 4999 copies/μL).Discussion: We provide the results from the first study of the use of the OSNA - one step nucleic acid amplification assay in colorectal cancer patients in Portugal. Our results are in-line with other international studies, showing the improvement on patients’ staging by molecular examination of lymph nodes.Conclusion: In our study, 28.8% of patients with histologically negative lymph nodes were found to have metastatic lymph nodes using OSNA - one step nucleic acid molecular assessment. OSNA - one step nucleic acid assay allows a more accurate staging of patients with colorectal cancer and standardizes lymph node assessment.Introdução: Cerca de 20% - 30% dos doentes com cancro colo-rectal, com gânglios linfáticos regionais negativos por histologia têm recidiva do carcinoma colo-rectal, após cinco anos do tratamento cirúrgico. Esta recorrência é provavelmente devida à presença de metástases ganglionares ocultas, não detetadas no exame anatomo-patológico standard.Material e Métodos: Os gânglios linfáticos foram obtidos a partir de espécimes de colectomia. Uma secção central de cada gânglio linfático foi analisada histologicamente com a coloração de hematoxilina-eosina e o tecido restante foi sujeito a análise de OSNA - one step nucleic acid amplification.Resultados: Um total de 1046 gânglios linfáticos de 59 doentes pN0 foram avaliados. Foram examinados 753 gânglios linfáticos por ambos os métodos. A mediana de gânglios linfáticos avaliados com OSNA - one step nucleic acid amplification foi de 12 (IQR:7; 16). Entre os doentes pN0, 17 tinham gânglios linfáticos positivos para OSNA - one step nucleic acid amplification, resultando numa taxa de estadiamento molecular positiva de 28,8% (95% CI: 17,8 - 42,1). De entre esses doentes, 12 (70,59%) apresentaram-se molecularmente pN1 e cinco (29,41%) pN2. A carga tumoral dos gânglios linfáticos avaliada com OSNA - one step nucleic acid amplification variou de 270 a 17 000 cópias/μL de ARNm de citoqueratina 19. A maioria desses doentes (88,2%) apresentou gânglios linfáticos com micrometástases (250 - 4999 cópias/μL).Discussão: Apresentamos os resultados do primeiro estudo do ensaio OSNA - one step nucleic acid amplification levado a cabo, em pacientes com cancro colo-rectal, em Portugal. Os nossos resultados estão em linha com outros estudos internacionais, demostrando uma melhoria no estadiamento dos doentes, pelo exame molecular dos gânglios linfáticos.Conclusão: Verificou-se que 28,8% dos doentes com gânglios linfáticos histologicamente negativos apresentavam doença ganglionar metastática, usando a avaliação molecular de OSNA - one step nucleic acid amplification. O ensaio OSNA - one step nucleic acid amplification permite um estadiamento mais preciso de doentes com carcinoma do colon e padroniza a avaliação dos gânglios linfáticos.Ordem dos Médicos2018-11-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696oai:ojs.www.actamedicaportuguesa.com:article/9696Acta Médica Portuguesa; Vol. 31 No. 11 (2018): November; 661-669Acta Médica Portuguesa; Vol. 31 N.º 11 (2018): Novembro; 661-6691646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/5553https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/9765https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10535https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10735https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10736https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10737https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10738Direitos de Autor (c) 2018 Acta Médica Portuguesainfo:eu-repo/semantics/openAccessBrito, María JoséHonavar, MrinaliniCipriano, Maria AugustaLopes, JoanneCoelho, HelderSilva, António Rodrigues daSilva, MárioGuimarães, SusanaFrutuoso, AmaroGomes, AnaBarbosa, ElisabeteCarlos, Sandra2022-12-20T11:05:47Zoai:ojs.www.actamedicaportuguesa.com:article/9696Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:19:44.520412Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
Estadiamento Molecular de Doentes com Carcinoma do Colon. O Estudo C-Closer-II: Um Estudo Multicêntrico em Portugal
title Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
spellingShingle Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
Brito, María José
Colorectal Neoplasms
Lymph Nodes
Lymphatic Metastasis
Neoplasm Staging
Nucleic Acid Amplification Techniques
Estadiamento de Neoplasias
Gânglios Linfáticos
Metástase Linfática
Neoplasias Colo-rectais
Técnicas de Amplificação de Ácido Nucleico
title_short Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
title_full Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
title_fullStr Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
title_full_unstemmed Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
title_sort Molecular Staging of Patients with Colon Cancer. The C-Closer-II Study: A Multicentre Study in Portugal
author Brito, María José
author_facet Brito, María José
Honavar, Mrinalini
Cipriano, Maria Augusta
Lopes, Joanne
Coelho, Helder
Silva, António Rodrigues da
Silva, Mário
Guimarães, Susana
Frutuoso, Amaro
Gomes, Ana
Barbosa, Elisabete
Carlos, Sandra
author_role author
author2 Honavar, Mrinalini
Cipriano, Maria Augusta
Lopes, Joanne
Coelho, Helder
Silva, António Rodrigues da
Silva, Mário
Guimarães, Susana
Frutuoso, Amaro
Gomes, Ana
Barbosa, Elisabete
Carlos, Sandra
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Brito, María José
Honavar, Mrinalini
Cipriano, Maria Augusta
Lopes, Joanne
Coelho, Helder
Silva, António Rodrigues da
Silva, Mário
Guimarães, Susana
Frutuoso, Amaro
Gomes, Ana
Barbosa, Elisabete
Carlos, Sandra
dc.subject.por.fl_str_mv Colorectal Neoplasms
Lymph Nodes
Lymphatic Metastasis
Neoplasm Staging
Nucleic Acid Amplification Techniques
Estadiamento de Neoplasias
Gânglios Linfáticos
Metástase Linfática
Neoplasias Colo-rectais
Técnicas de Amplificação de Ácido Nucleico
topic Colorectal Neoplasms
Lymph Nodes
Lymphatic Metastasis
Neoplasm Staging
Nucleic Acid Amplification Techniques
Estadiamento de Neoplasias
Gânglios Linfáticos
Metástase Linfática
Neoplasias Colo-rectais
Técnicas de Amplificação de Ácido Nucleico
description Introduction: Approximately 20% - 30% of histological lymph node-negative patients with colorectal cancer relapse at five years after surgical treatment. This recurrence is likely due to occult nodal disease undetected by standard histopathological practice which has implications in terms of the clinical management of patients.Material and Methods: Lymph nodes were collected from colectomy specimens. A central section from each lymph node was histologically examined following haematoxylin-eosin staining and the remaining tissue was subjected to OSNA - one step nucleic acid amplification analysis.Results: A total of 1046 lymph nodes from 59 pN0 patients were assessed. Of these, 753 lymph nodes were examined by both methods. The median number of lymph nodes assessed with OSNA - one step nucleic acid amplification was 12 (IQR: 7;16). Among pN0 patients, 17 had OSNA - one step nucleic acid amplification-positive lymph nodes, resulting in a positive molecular staging rate of 28.8% (95% CI: 17.8 - 42.1). Among these patients, 12 (70.59%) were molecular-staged as pN1 and 5 (29.41%) were molecular staged as pN2. The tumour burden of lymph nodes assessed with OSNA - one step nucleic acid amplification ranged from 270 to 17 000 cytokeratin 19 mRNA copies/μL. Most of these patients (88.2%) were found to have lymph nodes with micrometastases only (250 - 4999 copies/μL).Discussion: We provide the results from the first study of the use of the OSNA - one step nucleic acid amplification assay in colorectal cancer patients in Portugal. Our results are in-line with other international studies, showing the improvement on patients’ staging by molecular examination of lymph nodes.Conclusion: In our study, 28.8% of patients with histologically negative lymph nodes were found to have metastatic lymph nodes using OSNA - one step nucleic acid molecular assessment. OSNA - one step nucleic acid assay allows a more accurate staging of patients with colorectal cancer and standardizes lymph node assessment.
publishDate 2018
dc.date.none.fl_str_mv 2018-11-30
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dc.language.iso.fl_str_mv eng
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/9765
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10535
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10735
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10736
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10737
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/9696/10738
dc.rights.driver.fl_str_mv Direitos de Autor (c) 2018 Acta Médica Portuguesa
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Direitos de Autor (c) 2018 Acta Médica Portuguesa
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 31 No. 11 (2018): November; 661-669
Acta Médica Portuguesa; Vol. 31 N.º 11 (2018): Novembro; 661-669
1646-0758
0870-399X
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