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The negative prognostic impact of bone metastasis with a tumor mass
OBJECTIVE: Typically, bone metastasis causes osteolytic and osteoblastic lesions resulting from the interactions of tumor cells with osteoclasts and osteoblasts. In addition to these interactions, tumor tissues may grow inside bones and cause mass lesions. In the present study, we aimed to demonstra...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518841/ https://www.ncbi.nlm.nih.gov/pubmed/26247664 http://dx.doi.org/10.6061/clinics/2015(08)01 |
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author | Yücel, Birsen Celasun, Mustafa Gürol Öztoprak, Bilge Hasbek, Zekiye Bahar, Seher Kaçan, Turgut Bahçeci, Aykut Şeker, Mehmet Metin |
author_facet | Yücel, Birsen Celasun, Mustafa Gürol Öztoprak, Bilge Hasbek, Zekiye Bahar, Seher Kaçan, Turgut Bahçeci, Aykut Şeker, Mehmet Metin |
author_sort | Yücel, Birsen |
collection | PubMed |
description | OBJECTIVE: Typically, bone metastasis causes osteolytic and osteoblastic lesions resulting from the interactions of tumor cells with osteoclasts and osteoblasts. In addition to these interactions, tumor tissues may grow inside bones and cause mass lesions. In the present study, we aimed to demonstrate the negative impact of a tumor mass in a large cohort of patients with bone metastatic cancer. METHODS: Data from 335 patients with bone metastases were retrospectively reviewed. For the analysis, all patients were divided into three subgroups with respect to the type of bone metastasis: osteolytic, osteoblastic, or mixed. The patients were subsequently categorized as having bone metastasis with or without a tumor mass, and statistically significant differences in median survival and 2-year overall survival were observed between these patients (the median survival and 2-year overall survival were respectively 3 months and 16% in patients with a tumor mass and 11 months and 26% in patients without a tumor mass; p<0.001). RESULTS: According to multivariate analysis, the presence of bone metastasis with a tumor mass was found to be an independent prognostic factor (p=0.011, hazard ratio: 1.62, 95% confidence interval: 1.11–1.76). Bone metastasis with a tumor mass was more strongly associated with osteolytic lesions, other primary diseases (except for primary breast and prostate cancers), and spinal cord compression. CONCLUSION: Bone metastasis with a tumor mass is a strong and independent negative prognostic factor for survival in cancer patients. |
format | Online Article Text |
id | pubmed-4518841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-45188412015-08-17 The negative prognostic impact of bone metastasis with a tumor mass Yücel, Birsen Celasun, Mustafa Gürol Öztoprak, Bilge Hasbek, Zekiye Bahar, Seher Kaçan, Turgut Bahçeci, Aykut Şeker, Mehmet Metin Clinics (Sao Paulo) Clinical Science OBJECTIVE: Typically, bone metastasis causes osteolytic and osteoblastic lesions resulting from the interactions of tumor cells with osteoclasts and osteoblasts. In addition to these interactions, tumor tissues may grow inside bones and cause mass lesions. In the present study, we aimed to demonstrate the negative impact of a tumor mass in a large cohort of patients with bone metastatic cancer. METHODS: Data from 335 patients with bone metastases were retrospectively reviewed. For the analysis, all patients were divided into three subgroups with respect to the type of bone metastasis: osteolytic, osteoblastic, or mixed. The patients were subsequently categorized as having bone metastasis with or without a tumor mass, and statistically significant differences in median survival and 2-year overall survival were observed between these patients (the median survival and 2-year overall survival were respectively 3 months and 16% in patients with a tumor mass and 11 months and 26% in patients without a tumor mass; p<0.001). RESULTS: According to multivariate analysis, the presence of bone metastasis with a tumor mass was found to be an independent prognostic factor (p=0.011, hazard ratio: 1.62, 95% confidence interval: 1.11–1.76). Bone metastasis with a tumor mass was more strongly associated with osteolytic lesions, other primary diseases (except for primary breast and prostate cancers), and spinal cord compression. CONCLUSION: Bone metastasis with a tumor mass is a strong and independent negative prognostic factor for survival in cancer patients. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015-08 2015-08 /pmc/articles/PMC4518841/ /pubmed/26247664 http://dx.doi.org/10.6061/clinics/2015(08)01 Text en Copyright © 2015 Clinics http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Yücel, Birsen Celasun, Mustafa Gürol Öztoprak, Bilge Hasbek, Zekiye Bahar, Seher Kaçan, Turgut Bahçeci, Aykut Şeker, Mehmet Metin The negative prognostic impact of bone metastasis with a tumor mass |
title | The negative prognostic impact of bone metastasis with a tumor mass |
title_full | The negative prognostic impact of bone metastasis with a tumor mass |
title_fullStr | The negative prognostic impact of bone metastasis with a tumor mass |
title_full_unstemmed | The negative prognostic impact of bone metastasis with a tumor mass |
title_short | The negative prognostic impact of bone metastasis with a tumor mass |
title_sort | negative prognostic impact of bone metastasis with a tumor mass |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518841/ https://www.ncbi.nlm.nih.gov/pubmed/26247664 http://dx.doi.org/10.6061/clinics/2015(08)01 |
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