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Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases

A heterogeneous group of cancers for which the site of origin remains occult after detailed investigations is defined as carcinomas of unknown primary origin (CUPs). Because patients with CUP have a dismal prognosis, we have analyzed CUPs to highlight the implication of clinicopathologic factors rel...

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Autores principales: Choi, Junjeong, Nahm, Ji Hae, Kim, Sang Kyum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617535/
https://www.ncbi.nlm.nih.gov/pubmed/28977975
http://dx.doi.org/10.18632/oncotarget.16021
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author Choi, Junjeong
Nahm, Ji Hae
Kim, Sang Kyum
author_facet Choi, Junjeong
Nahm, Ji Hae
Kim, Sang Kyum
author_sort Choi, Junjeong
collection PubMed
description A heterogeneous group of cancers for which the site of origin remains occult after detailed investigations is defined as carcinomas of unknown primary origin (CUPs). Because patients with CUP have a dismal prognosis, we have analyzed CUPs to highlight the implication of clinicopathologic factors related with patient survival. A total of 106 consecutive cases of CUP were collected. A two-step strategy of immunohistochemistry to assess CUPs according NCCN Guidelines is used to separate carcinomatous tumors and subtype carcinomas. Median follow up of censored patients was 26 months. Median survival time of whole patients was 13 months (95% confidence interval [CI], 8.43 - 19.1 months), with one, two and five-year survival rate of 53.7%, 35.1%, and 30.5%, respectively. Factors related with shorter overall survival was adenocarcinoma histology (P=0.001), increased CA19-9 (P=0.003), increased CEA (P=0.047), increased LDH (P<0.001), CK20 positivity (P=0.002), presence of bone metastasis (P=0.017), metastasis not confined to the lymph nodes (P=0.015), unfavorable clinical group based predefined category (P=0.017), and patients with no treatment (P<0.001). Multivariable analysis with cox regression model revealed factors related with overall survival; cases belonged to Culine’s poor risk group (HR, 3.88; 95% CI, 1.75-8.64; P=0.001) and CK20 positivity (HR, 3.31; 95% CI, 1.42-7.70; P=0.005). In conclusion, the CK20 expression profile is a prognostic factor in patients with CUP and initial stratification of patient with Culine’s model may provide a prognostic information in these patients. Assessment of clinical implication of these factors in the context of site specific therapy needs to be evaluated.
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spelling pubmed-56175352017-10-03 Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases Choi, Junjeong Nahm, Ji Hae Kim, Sang Kyum Oncotarget Clinical Research Paper A heterogeneous group of cancers for which the site of origin remains occult after detailed investigations is defined as carcinomas of unknown primary origin (CUPs). Because patients with CUP have a dismal prognosis, we have analyzed CUPs to highlight the implication of clinicopathologic factors related with patient survival. A total of 106 consecutive cases of CUP were collected. A two-step strategy of immunohistochemistry to assess CUPs according NCCN Guidelines is used to separate carcinomatous tumors and subtype carcinomas. Median follow up of censored patients was 26 months. Median survival time of whole patients was 13 months (95% confidence interval [CI], 8.43 - 19.1 months), with one, two and five-year survival rate of 53.7%, 35.1%, and 30.5%, respectively. Factors related with shorter overall survival was adenocarcinoma histology (P=0.001), increased CA19-9 (P=0.003), increased CEA (P=0.047), increased LDH (P<0.001), CK20 positivity (P=0.002), presence of bone metastasis (P=0.017), metastasis not confined to the lymph nodes (P=0.015), unfavorable clinical group based predefined category (P=0.017), and patients with no treatment (P<0.001). Multivariable analysis with cox regression model revealed factors related with overall survival; cases belonged to Culine’s poor risk group (HR, 3.88; 95% CI, 1.75-8.64; P=0.001) and CK20 positivity (HR, 3.31; 95% CI, 1.42-7.70; P=0.005). In conclusion, the CK20 expression profile is a prognostic factor in patients with CUP and initial stratification of patient with Culine’s model may provide a prognostic information in these patients. Assessment of clinical implication of these factors in the context of site specific therapy needs to be evaluated. Impact Journals LLC 2017-03-08 /pmc/articles/PMC5617535/ /pubmed/28977975 http://dx.doi.org/10.18632/oncotarget.16021 Text en Copyright: © 2017 Choi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Choi, Junjeong
Nahm, Ji Hae
Kim, Sang Kyum
Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title_full Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title_fullStr Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title_full_unstemmed Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title_short Prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
title_sort prognostic clinicopathologic factors in carcinoma of unknown primary origin: a study of 106 consecutive cases
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617535/
https://www.ncbi.nlm.nih.gov/pubmed/28977975
http://dx.doi.org/10.18632/oncotarget.16021
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