Malignant fibrous histiocytoma of bone: A survival analysis from the National Cancer Database

Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH...

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Published inJournal of surgical oncology Vol. 121; no. 7; pp. 1097 - 1103
Main Authors Malik, Azeem T., Baek, Jae, Alexander, John H., Voskuil, Ryan T., Khan, Safdar N., Scharschmidt, Thomas J.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.06.2020
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Abstract Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH of bone. Methods The 2004 to 2016 National Cancer Database was queried to identify patients with a primary MFH of bone. Kaplan‐Meier survival and Cox regression analyses were used to analyze overall survival and risk factors associated with overall mortality. Results The overall 5‐year and 10‐year survival rates were 38.3% and 30.5%, respectively. Increasing stage and metastatic disease at presentation were associated with poor overall survival (P < .001). Patients aged 18 to 50 years (hazard ratio [HR], 0.51), 51 to 75 years (HR, 0.61), and those undergoing surgery (HR, 0.39) had improved survival. Having Medicare insurance (HR, 1.48), residing in a low educated area (HR, 2.56), and positive surgical margins (HR, 1.80) were associated with poor survival. Conclusions The overall prognosis of MFH of bone is poor with a reported 5‐year survival rate of 38.3%. Undergoing surgery and younger age were associated with a better prognosis. Older age, having Medicare insurance, and positive surgical margins were predictors of mortality.
AbstractList Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH of bone. The 2004 to 2016 National Cancer Database was queried to identify patients with a primary MFH of bone. Kaplan-Meier survival and Cox regression analyses were used to analyze overall survival and risk factors associated with overall mortality. The overall 5-year and 10-year survival rates were 38.3% and 30.5%, respectively. Increasing stage and metastatic disease at presentation were associated with poor overall survival (P < .001). Patients aged 18 to 50 years (hazard ratio [HR], 0.51), 51 to 75 years (HR, 0.61), and those undergoing surgery (HR, 0.39) had improved survival. Having Medicare insurance (HR, 1.48), residing in a low educated area (HR, 2.56), and positive surgical margins (HR, 1.80) were associated with poor survival. The overall prognosis of MFH of bone is poor with a reported 5-year survival rate of 38.3%. Undergoing surgery and younger age were associated with a better prognosis. Older age, having Medicare insurance, and positive surgical margins were predictors of mortality.
BACKGROUND AND OBJECTIVESMalignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH of bone. METHODSThe 2004 to 2016 National Cancer Database was queried to identify patients with a primary MFH of bone. Kaplan-Meier survival and Cox regression analyses were used to analyze overall survival and risk factors associated with overall mortality. RESULTSThe overall 5-year and 10-year survival rates were 38.3% and 30.5%, respectively. Increasing stage and metastatic disease at presentation were associated with poor overall survival (P < .001). Patients aged 18 to 50 years (hazard ratio [HR], 0.51), 51 to 75 years (HR, 0.61), and those undergoing surgery (HR, 0.39) had improved survival. Having Medicare insurance (HR, 1.48), residing in a low educated area (HR, 2.56), and positive surgical margins (HR, 1.80) were associated with poor survival. CONCLUSIONSThe overall prognosis of MFH of bone is poor with a reported 5-year survival rate of 38.3%. Undergoing surgery and younger age were associated with a better prognosis. Older age, having Medicare insurance, and positive surgical margins were predictors of mortality.
Abstract Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH of bone. Methods The 2004 to 2016 National Cancer Database was queried to identify patients with a primary MFH of bone. Kaplan‐Meier survival and Cox regression analyses were used to analyze overall survival and risk factors associated with overall mortality. Results The overall 5‐year and 10‐year survival rates were 38.3% and 30.5%, respectively. Increasing stage and metastatic disease at presentation were associated with poor overall survival ( P  < .001). Patients aged 18 to 50 years (hazard ratio [HR], 0.51), 51 to 75 years (HR, 0.61), and those undergoing surgery (HR, 0.39) had improved survival. Having Medicare insurance (HR, 1.48), residing in a low educated area (HR, 2.56), and positive surgical margins (HR, 1.80) were associated with poor survival. Conclusions The overall prognosis of MFH of bone is poor with a reported 5‐year survival rate of 38.3%. Undergoing surgery and younger age were associated with a better prognosis. Older age, having Medicare insurance, and positive surgical margins were predictors of mortality.
Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of all primary malignant bone tumors. The objective of the current study was to evaluate prognosis and survival for MFH of bone. Methods The 2004 to 2016 National Cancer Database was queried to identify patients with a primary MFH of bone. Kaplan‐Meier survival and Cox regression analyses were used to analyze overall survival and risk factors associated with overall mortality. Results The overall 5‐year and 10‐year survival rates were 38.3% and 30.5%, respectively. Increasing stage and metastatic disease at presentation were associated with poor overall survival (P < .001). Patients aged 18 to 50 years (hazard ratio [HR], 0.51), 51 to 75 years (HR, 0.61), and those undergoing surgery (HR, 0.39) had improved survival. Having Medicare insurance (HR, 1.48), residing in a low educated area (HR, 2.56), and positive surgical margins (HR, 1.80) were associated with poor survival. Conclusions The overall prognosis of MFH of bone is poor with a reported 5‐year survival rate of 38.3%. Undergoing surgery and younger age were associated with a better prognosis. Older age, having Medicare insurance, and positive surgical margins were predictors of mortality.
Author Scharschmidt, Thomas J.
Khan, Safdar N.
Malik, Azeem T.
Baek, Jae
Voskuil, Ryan T.
Alexander, John H.
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Keywords malignant fibrous histiocytoma
undifferentiated pleomorphic sarcoma
NCDB
survival
UPS
MFH
bone sarcoma
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  doi: 10.1007/s00132-006-1017-8
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Snippet Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that...
Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that accounts for less than 2% of...
Abstract Background and Objectives Malignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm...
Background and ObjectivesMalignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that...
BACKGROUND AND OBJECTIVESMalignant fibrous histiocytoma (MFH) of bone, now known as undifferentiated pleomorphic sarcoma of bone, is a rare neoplasm that...
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pubmed
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage 1097
SubjectTerms Adolescent
Adult
Aged
Bone cancer
Bone Neoplasms - mortality
Bone Neoplasms - pathology
bone sarcoma
Databases, Factual
Female
Histiocytoma, Malignant Fibrous - mortality
Histiocytoma, Malignant Fibrous - pathology
Humans
Kaplan-Meier Estimate
Male
malignant fibrous histiocytoma
Medical prognosis
Medicare
MFH
Middle Aged
Mortality
NCDB
Proportional Hazards Models
Retrospective Studies
Sarcoma
survival
Survival analysis
undifferentiated pleomorphic sarcoma
United States - epidemiology
UPS
Young Adult
Title Malignant fibrous histiocytoma of bone: A survival analysis from the National Cancer Database
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjso.25878
https://www.ncbi.nlm.nih.gov/pubmed/32133661
https://www.proquest.com/docview/2396505830
https://search.proquest.com/docview/2371867359
Volume 121
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