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Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease
AIMS: The modern prevalence of primary tumours causing metastatic bone disease is ill-defined in the oncological literature. Therefore, the purpose of this study is to identify the prevalence of primary tumours in the setting of metastatic bone disease, as well as reported rates of pathological frac...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Editorial Society of Bone & Joint Surgery
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240245/ https://www.ncbi.nlm.nih.gov/pubmed/37272304 http://dx.doi.org/10.1302/2633-1462.46.BJO-2023-0042.R1 |
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author | Christ, Alexander B. Piple, Amit S. Gettleman, Brandon S. Duong, Andrew Chen, Matthew Wang, Jennifer C. Heckmann, Nathanael D. Menendez, Lawrence |
author_facet | Christ, Alexander B. Piple, Amit S. Gettleman, Brandon S. Duong, Andrew Chen, Matthew Wang, Jennifer C. Heckmann, Nathanael D. Menendez, Lawrence |
author_sort | Christ, Alexander B. |
collection | PubMed |
description | AIMS: The modern prevalence of primary tumours causing metastatic bone disease is ill-defined in the oncological literature. Therefore, the purpose of this study is to identify the prevalence of primary tumours in the setting of metastatic bone disease, as well as reported rates of pathological fracture, postoperative complications, 90-day mortality, and 360-day mortality for each primary tumour subtype. METHODS: The Premier Healthcare Database was queried to identify all patients who were diagnosed with metastatic bone disease from January 2015 to December 2020. The prevalence of all primary tumour subtypes was tabulated. Rates of long bone pathological fracture, 90-day mortality, and 360-day mortality following surgical treatment of pathological fracture were assessed for each primary tumour subtype. Patient characteristics and postoperative outcomes were analyzed based upon whether patients had impending fractures treated prophylactically versus treated completed fractures. RESULTS: In total, 407,893 unique patients with metastatic bone disease were identified. Of the 14 primary tumours assessed, metastatic bone disease most frequently originated from lung (24.8%), prostatic (19.4%), breast (19.3%), gastrointestinal (9.4%), and urological (6.5%) malignancies. The top five malignant tumours resulting in long bone pathological fracture were renal (5.8%), myeloma (3.4%), female reproductive (3.2%), lung (2.8%), and breast (2.7%). Following treatment of pathological fractures of long bones, 90-day mortality rates were greatest for lung (12.1%), central nervous system (10.5%), lymphoma (10.4%), gastrointestinal (10.1%), and non-renal urinary (10.0%) malignancies. Finally, our study demonstrates improved 90-day and 360-day survival in patients treated for impending pathological fracture compared to completed fracture, as well as significantly lower rates of deep vein thrombosis, pulmonary embolism, urinary tract infection, and blood transfusion. CONCLUSION: This study defines the contemporary characteristics of primary malignancies resulting in metastatic bone disease. These data should be considered by surgeons when prognosticating patient outcomes during treatment of their metastatic bone disease. Cite this article: Bone Jt Open 2023;4(6):424–431. |
format | Online Article Text |
id | pubmed-10240245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The British Editorial Society of Bone & Joint Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-102402452023-06-06 Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease Christ, Alexander B. Piple, Amit S. Gettleman, Brandon S. Duong, Andrew Chen, Matthew Wang, Jennifer C. Heckmann, Nathanael D. Menendez, Lawrence Bone Jt Open Oncology AIMS: The modern prevalence of primary tumours causing metastatic bone disease is ill-defined in the oncological literature. Therefore, the purpose of this study is to identify the prevalence of primary tumours in the setting of metastatic bone disease, as well as reported rates of pathological fracture, postoperative complications, 90-day mortality, and 360-day mortality for each primary tumour subtype. METHODS: The Premier Healthcare Database was queried to identify all patients who were diagnosed with metastatic bone disease from January 2015 to December 2020. The prevalence of all primary tumour subtypes was tabulated. Rates of long bone pathological fracture, 90-day mortality, and 360-day mortality following surgical treatment of pathological fracture were assessed for each primary tumour subtype. Patient characteristics and postoperative outcomes were analyzed based upon whether patients had impending fractures treated prophylactically versus treated completed fractures. RESULTS: In total, 407,893 unique patients with metastatic bone disease were identified. Of the 14 primary tumours assessed, metastatic bone disease most frequently originated from lung (24.8%), prostatic (19.4%), breast (19.3%), gastrointestinal (9.4%), and urological (6.5%) malignancies. The top five malignant tumours resulting in long bone pathological fracture were renal (5.8%), myeloma (3.4%), female reproductive (3.2%), lung (2.8%), and breast (2.7%). Following treatment of pathological fractures of long bones, 90-day mortality rates were greatest for lung (12.1%), central nervous system (10.5%), lymphoma (10.4%), gastrointestinal (10.1%), and non-renal urinary (10.0%) malignancies. Finally, our study demonstrates improved 90-day and 360-day survival in patients treated for impending pathological fracture compared to completed fracture, as well as significantly lower rates of deep vein thrombosis, pulmonary embolism, urinary tract infection, and blood transfusion. CONCLUSION: This study defines the contemporary characteristics of primary malignancies resulting in metastatic bone disease. These data should be considered by surgeons when prognosticating patient outcomes during treatment of their metastatic bone disease. Cite this article: Bone Jt Open 2023;4(6):424–431. The British Editorial Society of Bone & Joint Surgery 2023-06-05 /pmc/articles/PMC10240245/ /pubmed/37272304 http://dx.doi.org/10.1302/2633-1462.46.BJO-2023-0042.R1 Text en © 2023 Authors et al. https://creativecommons.org/licenses/by-nc-nd/4.0/https://online.boneandjoint.org.uk/TDMThis is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Oncology Christ, Alexander B. Piple, Amit S. Gettleman, Brandon S. Duong, Andrew Chen, Matthew Wang, Jennifer C. Heckmann, Nathanael D. Menendez, Lawrence Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title | Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title_full | Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title_fullStr | Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title_full_unstemmed | Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title_short | Prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
title_sort | prevalence of primary malignant tumours, rates of pathological fracture, and mortality in the setting of metastatic bone disease |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240245/ https://www.ncbi.nlm.nih.gov/pubmed/37272304 http://dx.doi.org/10.1302/2633-1462.46.BJO-2023-0042.R1 |
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