Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status
Descripción del Articulo
Objectives: the main goal for this study was to evaluate overall survival in mCRC patients with mutated vs. wild type KRAS gene (exon 2) status. Materials and methods: between January 2010 and December 2013, data from clinical records of mCRC patients from different hospitals in Lima, stating an ass...
Autor: | |
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Formato: | artículo |
Fecha de Publicación: | 2020 |
Institución: | Colegio Médico del Perú |
Repositorio: | Acta Médica Peruana |
Lenguaje: | español |
OAI Identifier: | oai:ojs.pkp.sfu.ca:article/868 |
Enlace del recurso: | https://amp.cmp.org.pe/index.php/AMP/article/view/868 |
Nivel de acceso: | acceso abierto |
Materia: | Cancer, colorectal /genetics Mutation Exons |
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Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational statusSupervivencia global del cáncer colorrectal metastásico en Lima Metropolitana: relación con el estado mutacional del gen KRASAldecoa, FranklinCancer, colorectal/geneticsMutationExonsObjectives: the main goal for this study was to evaluate overall survival in mCRC patients with mutated vs. wild type KRAS gene (exon 2) status. Materials and methods: between January 2010 and December 2013, data from clinical records of mCRC patients from different hospitals in Lima, stating an assessment of the KRAS gene mutation status (exon 2), were analyzed. Kaplan-Meier survival estimates and Log-Rank or Breslow Test were used to compare the survival curves. Results: three-hundred and twenty cases were analyzed. There were 227 patients (70.93%) with wild type KRAS and 93 (29.07%) with mutated KRAS. The overall survival of mCRC patients and mutated KRAS was higher than that of patients with wild type KRAS (HR: 0.73; 95% CI: 0.55–0.98; P= 0.037). Conclusion: patients with mCRC and mutated KRAS who were studied in Lima have higher survival rates compared to wild type patients, being this different from what is found in the world literature.Objetivos: el objetivo principal del estudio fue evaluar la supervivencia global en pacientes con carcinoma colorrectal metastásico (CCRm) cuyos tumores tuvieran el gen KRAS mutado frente al no mutado. Materiales y métodos: se analizaron los datos de las historias clínicas de pacientes con CCRm (enero 2010 - diciembre 2013) de diferentes hospitales de Lima Metropolitana, cuyos tumores tuvieron evaluación del estado mutacional del exón 2, gen KRAS. Se usaron la curva de supervivencia de Kaplan-Meier y la prueba de long rank o Breslow para las comparaciones de las curvas de supervivencia. Resultados: de los 320 casos analizados, hubo 227 pacientes (70,93%) con KRAS no mutado y 93 (29,07%) con KRAS mutado. La supervivencia global de pacientes con CCRm y KRAS mutado fue mayor que los pacientes con KRAS no mutado (hazart ratio: 0,73; IC 95% 0,55 – 0,98; p=0,037). Conclusión: la población con CCRm y KRAS mutado estudiada en centros médicos de Lima Metropolitana tuvo una supervivencia mayor, comparada con la no mutada, comportamiento diferente a lo encontrado en la literatura mundial.Colegio Médico del Perú2020-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://amp.cmp.org.pe/index.php/AMP/article/view/86810.35663/amp.2020.372.868ACTA MEDICA PERUANA; Vol 37 No 2 (2020): April - JuneACTA MEDICA PERUANA; Vol. 37 Núm. 2 (2020): Abril - Junio1728-59171018-8800reponame:Acta Médica Peruanainstname:Colegio Médico del Perúinstacron:CMPspahttps://amp.cmp.org.pe/index.php/AMP/article/view/868/437Copyright (c) 2020 ACTA MEDICA PERUANAinfo:eu-repo/semantics/openAccessoai:ojs.pkp.sfu.ca:article/8682023-07-06T05:50:52Z |
dc.title.none.fl_str_mv |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status Supervivencia global del cáncer colorrectal metastásico en Lima Metropolitana: relación con el estado mutacional del gen KRAS |
title |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
spellingShingle |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status Aldecoa, Franklin Cancer, colorectal /genetics Mutation Exons |
title_short |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
title_full |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
title_fullStr |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
title_full_unstemmed |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
title_sort |
Overall survival of metastatic colorectal cancer in Lima: relationship with the KRAS gene mutational status |
dc.creator.none.fl_str_mv |
Aldecoa, Franklin |
author |
Aldecoa, Franklin |
author_facet |
Aldecoa, Franklin |
author_role |
author |
dc.subject.none.fl_str_mv |
Cancer, colorectal /genetics Mutation Exons |
topic |
Cancer, colorectal /genetics Mutation Exons |
description |
Objectives: the main goal for this study was to evaluate overall survival in mCRC patients with mutated vs. wild type KRAS gene (exon 2) status. Materials and methods: between January 2010 and December 2013, data from clinical records of mCRC patients from different hospitals in Lima, stating an assessment of the KRAS gene mutation status (exon 2), were analyzed. Kaplan-Meier survival estimates and Log-Rank or Breslow Test were used to compare the survival curves. Results: three-hundred and twenty cases were analyzed. There were 227 patients (70.93%) with wild type KRAS and 93 (29.07%) with mutated KRAS. The overall survival of mCRC patients and mutated KRAS was higher than that of patients with wild type KRAS (HR: 0.73; 95% CI: 0.55–0.98; P= 0.037). Conclusion: patients with mCRC and mutated KRAS who were studied in Lima have higher survival rates compared to wild type patients, being this different from what is found in the world literature. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-07-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://amp.cmp.org.pe/index.php/AMP/article/view/868 10.35663/amp.2020.372.868 |
url |
https://amp.cmp.org.pe/index.php/AMP/article/view/868 |
identifier_str_mv |
10.35663/amp.2020.372.868 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
https://amp.cmp.org.pe/index.php/AMP/article/view/868/437 |
dc.rights.none.fl_str_mv |
Copyright (c) 2020 ACTA MEDICA PERUANA info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2020 ACTA MEDICA PERUANA |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Colegio Médico del Perú |
publisher.none.fl_str_mv |
Colegio Médico del Perú |
dc.source.none.fl_str_mv |
ACTA MEDICA PERUANA; Vol 37 No 2 (2020): April - June ACTA MEDICA PERUANA; Vol. 37 Núm. 2 (2020): Abril - Junio 1728-5917 1018-8800 reponame:Acta Médica Peruana instname:Colegio Médico del Perú instacron:CMP |
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Colegio Médico del Perú |
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CMP |
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CMP |
reponame_str |
Acta Médica Peruana |
collection |
Acta Médica Peruana |
repository.name.fl_str_mv |
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repository.mail.fl_str_mv |
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1816075103017893888 |
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13.889614 |
Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).