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Published in: BMC Musculoskeletal Disorders 1/2020

Open Access 01-12-2020 | Research article

Malignant fibrous neoplasms of long bones: analysis of the surveillance, epidemiology, and end results database from 1973 to 2015

Authors: Yiting Huang, Jianqiao Hong, Jiahong Meng, Haobo Wu, Mingmin Shi, Shigui Yan, Wei Wang

Published in: BMC Musculoskeletal Disorders | Issue 1/2020

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Abstract

Background

Malignant fibrous neoplasms (MFN) of long bones are rare lesions. Moreover, the prognostic determinants of MFN of long bones have not been reported. This study aimed to present epidemiological data and analyse the prognostic factors for survival in patients with MFN.

Materials and methods

The Surveillance, Epidemiology, and End Results (SEER) programme database was used to screen patients with malignant fibrous neoplasms (MFN) of long bones from 1973 to 2015, with attention to fibrosarcoma, fibromyxosarcoma, periosteal fibrosarcoma and malignant fibrous histiocytoma. The prognostic values of overall survival (OS) and cancer-specific survival (CSS) were assessed using the Cox proportional hazards regression model with univariate and multivariate analyses. The Kaplan–Meier method was used to obtain OS and CSS curves.

Results

A total of 237 cases were selected from the SEER database. Malignant fibrous histiocytoma was the most common form of lesion in long bones. Multivariate analysis revealed that independent predictors of OS included age, stage, tumour size and surgery. Age, stage, tumour size and surgery were also independent predictors of CSS. Additionally, the most significant prognostic factor was whether metastasis had occurred at the time of initial diagnosis.

Conclusion

Among patients with MFN of long bones, age (> 60 years), tumour size (> 10 cm), distant stage, and non-surgical treatment are factors for poor survival.
Literature
1.
go back to reference Belal A, Kandil A, Allam A, Khafaga Y, El-Husseiny G, El-Enbaby A, Memon M, Younge D, Moreau P, Gray A, et al. Malignant fibrous histiocytoma: a retrospective study of 109 cases. Am J Clin Oncol. 2002;25(1):16–22.CrossRef Belal A, Kandil A, Allam A, Khafaga Y, El-Husseiny G, El-Enbaby A, Memon M, Younge D, Moreau P, Gray A, et al. Malignant fibrous histiocytoma: a retrospective study of 109 cases. Am J Clin Oncol. 2002;25(1):16–22.CrossRef
2.
go back to reference Heffner DK, Gnepp DR. Sinonasal fibrosarcomas, malignant schwannomas, and “triton” tumors. A clinicopathologic study of 67 cases. Cancer. 1992;70(5):1089–101.CrossRef Heffner DK, Gnepp DR. Sinonasal fibrosarcomas, malignant schwannomas, and “triton” tumors. A clinicopathologic study of 67 cases. Cancer. 1992;70(5):1089–101.CrossRef
3.
go back to reference Ozzello L, Stout AP, Murray MR. Cultural characteristics of malignant histiocytomas and fibrous xanthomas. Cancer. 1963;16:331–44.CrossRef Ozzello L, Stout AP, Murray MR. Cultural characteristics of malignant histiocytomas and fibrous xanthomas. Cancer. 1963;16:331–44.CrossRef
4.
go back to reference Kauffman SL, Stout AP. Histiocytic tumors (fibrous xanthoma and histiocytoma) in children. Cancer. 1961;14:469–82.CrossRef Kauffman SL, Stout AP. Histiocytic tumors (fibrous xanthoma and histiocytoma) in children. Cancer. 1961;14:469–82.CrossRef
5.
go back to reference Simons A, Schepens M, Jeuken J, Sprenger S, van de Zande G, Bjerkehagen B, Forus A, Weibolt V, Molenaar I, van den Berg E, et al. Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma. Cancer Genet Cytogenet. 2000;118(2):89–98.CrossRef Simons A, Schepens M, Jeuken J, Sprenger S, van de Zande G, Bjerkehagen B, Forus A, Weibolt V, Molenaar I, van den Berg E, et al. Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma. Cancer Genet Cytogenet. 2000;118(2):89–98.CrossRef
6.
go back to reference Fu YS, Perzin KH. Nonepithelial tumors of the nasal cavity, paranasal sinuses, and nasopharynx. A clinicopathologic study. VI. Fibrous tissue tumors (fibroma, fibromatosis, fibrosarcoma). Cancer. 1976;37(6):2912–28.CrossRef Fu YS, Perzin KH. Nonepithelial tumors of the nasal cavity, paranasal sinuses, and nasopharynx. A clinicopathologic study. VI. Fibrous tissue tumors (fibroma, fibromatosis, fibrosarcoma). Cancer. 1976;37(6):2912–28.CrossRef
7.
go back to reference Ozkurt B, Basarir K, Yildiz YH, Kalem M, Saglik Y. Primary malignant fibrous histiocytoma of long bones: long-term follow-up. Eklem Hastalik Cerrahisi. 2016;27(2):94–9.CrossRef Ozkurt B, Basarir K, Yildiz YH, Kalem M, Saglik Y. Primary malignant fibrous histiocytoma of long bones: long-term follow-up. Eklem Hastalik Cerrahisi. 2016;27(2):94–9.CrossRef
8.
go back to reference Niu Q, Lu Y, Xu S, Shi Q, Guo B, Guo Z, Huang T, Wu Y, Yu J. Clinicopathological characteristics and survival outcomes of bladder neuroendocrine carcinomas: a population-based study. Cancer Manag Res. 2018;10:4479–89.CrossRef Niu Q, Lu Y, Xu S, Shi Q, Guo B, Guo Z, Huang T, Wu Y, Yu J. Clinicopathological characteristics and survival outcomes of bladder neuroendocrine carcinomas: a population-based study. Cancer Manag Res. 2018;10:4479–89.CrossRef
9.
go back to reference Ge LP, Liu XY, Xiao Y, Gou ZC, Zhao S, Jiang YZ, Di GH. Clinicopathological characteristics and treatment outcomes of occult breast cancer: a SEER population-based study. Cancer Manag Res. 2018;10:4381–91.CrossRef Ge LP, Liu XY, Xiao Y, Gou ZC, Zhao S, Jiang YZ, Di GH. Clinicopathological characteristics and treatment outcomes of occult breast cancer: a SEER population-based study. Cancer Manag Res. 2018;10:4381–91.CrossRef
10.
go back to reference Wu G, Wu J, Wang B, Zhu X, Shi X, Ding Y. Importance of tumor size at diagnosis as a prognostic factor for hepatocellular carcinoma survival: a population-based study. Cancer Manag Res. 2018;10:4401–10.CrossRef Wu G, Wu J, Wang B, Zhu X, Shi X, Ding Y. Importance of tumor size at diagnosis as a prognostic factor for hepatocellular carcinoma survival: a population-based study. Cancer Manag Res. 2018;10:4401–10.CrossRef
11.
go back to reference Pan Y, Lu L, Chen J, Zhong Y, Dai Z. Analysis of prognostic factors for survival in patients with primary spinal chordoma using the SEER registry from 1973 to 2014. J Orthop Surg Res. 2018;13(1):76.CrossRef Pan Y, Lu L, Chen J, Zhong Y, Dai Z. Analysis of prognostic factors for survival in patients with primary spinal chordoma using the SEER registry from 1973 to 2014. J Orthop Surg Res. 2018;13(1):76.CrossRef
12.
go back to reference Ren S, Wang Z, Huang X, Sun L, Shao J, Ye Z. Prognostic factors for postoperative survival among patients with rhabdomyosarcoma of the limbs. Cancer Manag Res. 2018;10:4181–9.CrossRef Ren S, Wang Z, Huang X, Sun L, Shao J, Ye Z. Prognostic factors for postoperative survival among patients with rhabdomyosarcoma of the limbs. Cancer Manag Res. 2018;10:4181–9.CrossRef
13.
go back to reference Patel TD, Carniol ET, Vazquez A, Baredes S, Liu JK, Eloy JA. Sinonasal fibrosarcoma: analysis of the surveillance, epidemiology, and end results database. Int Forum Allergy Rhinol. 2016;6(2):201–5.CrossRef Patel TD, Carniol ET, Vazquez A, Baredes S, Liu JK, Eloy JA. Sinonasal fibrosarcoma: analysis of the surveillance, epidemiology, and end results database. Int Forum Allergy Rhinol. 2016;6(2):201–5.CrossRef
14.
go back to reference Rubio GA, Alvarado A, Gerth DJ, Tashiro J, Thaller SR. Incidence and outcomes of Dermatofibrosarcoma Protuberans in the US pediatric population. J Craniofac Surg. 2017;28(1):182–4.CrossRef Rubio GA, Alvarado A, Gerth DJ, Tashiro J, Thaller SR. Incidence and outcomes of Dermatofibrosarcoma Protuberans in the US pediatric population. J Craniofac Surg. 2017;28(1):182–4.CrossRef
15.
go back to reference Tseng WH, Martinez SR, Do L, Tamurian RM, Borys D, Canter RJ. Lack of survival benefit following adjuvant radiation in patients with retroperitoneal sarcoma: a SEER analysis. J Surg Res. 2011;168(2):e173–80.CrossRef Tseng WH, Martinez SR, Do L, Tamurian RM, Borys D, Canter RJ. Lack of survival benefit following adjuvant radiation in patients with retroperitoneal sarcoma: a SEER analysis. J Surg Res. 2011;168(2):e173–80.CrossRef
16.
go back to reference Borucki RB, Neskey DM, Lentsch EJ. Malignant fibrous histiocytoma: database review suggests a favorable prognosis in the head and neck. Laryngoscope. 2018;128(4):885–8.CrossRef Borucki RB, Neskey DM, Lentsch EJ. Malignant fibrous histiocytoma: database review suggests a favorable prognosis in the head and neck. Laryngoscope. 2018;128(4):885–8.CrossRef
17.
go back to reference Tseng W, Martinez SR, Tamurian RM, Borys D, Canter RJ. Histologic type predicts survival in patients with retroperitoneal soft tissue sarcoma. J Surg Res. 2012;172(1):123–30.CrossRef Tseng W, Martinez SR, Tamurian RM, Borys D, Canter RJ. Histologic type predicts survival in patients with retroperitoneal soft tissue sarcoma. J Surg Res. 2012;172(1):123–30.CrossRef
18.
go back to reference Campschroer T, van der Kwast TH, Jonges GN, Lock MT. Angiosarcoma of the prostate: a more frequent finding in the future owing to radiotherapy? A literature review with treatment implications based on a case report. Scand J Urol. 2014;48(5):420–5.CrossRef Campschroer T, van der Kwast TH, Jonges GN, Lock MT. Angiosarcoma of the prostate: a more frequent finding in the future owing to radiotherapy? A literature review with treatment implications based on a case report. Scand J Urol. 2014;48(5):420–5.CrossRef
19.
go back to reference Matushansky I, Dela CF, Insel BJ, Hershman DL, Neugut AI. Chemotherapy use in elderly patients with soft tissue sarcoma: a population-based study. Cancer Investig. 2013;31(2):83–91.CrossRef Matushansky I, Dela CF, Insel BJ, Hershman DL, Neugut AI. Chemotherapy use in elderly patients with soft tissue sarcoma: a population-based study. Cancer Investig. 2013;31(2):83–91.CrossRef
20.
go back to reference Doyle LA. Sarcoma classification: an update based on the 2013 World Health Organization classification of tumors of soft tissue and bone. Cancer. 2014;120(12):1763–74.CrossRef Doyle LA. Sarcoma classification: an update based on the 2013 World Health Organization classification of tumors of soft tissue and bone. Cancer. 2014;120(12):1763–74.CrossRef
21.
go back to reference Wang Z, Li S, Li Y, Lin N, Huang X, Liu M, Pan W, Yan X, Sun L, Li H, et al. Prognostic factors for survival among patients with primary bone sarcomas of small bones. Cancer Manag Res. 2018;10:1191–9.CrossRef Wang Z, Li S, Li Y, Lin N, Huang X, Liu M, Pan W, Yan X, Sun L, Li H, et al. Prognostic factors for survival among patients with primary bone sarcomas of small bones. Cancer Manag Res. 2018;10:1191–9.CrossRef
22.
go back to reference Williams N, Morris CG, Kirwan JM, Dagan R, Mendenhall WM. Radiotherapy for dermatofibrosarcoma protuberans. Am J Clin Oncol. 2014;37(5):430–2.CrossRef Williams N, Morris CG, Kirwan JM, Dagan R, Mendenhall WM. Radiotherapy for dermatofibrosarcoma protuberans. Am J Clin Oncol. 2014;37(5):430–2.CrossRef
23.
go back to reference Salerni G, Alonso C, Sanchez-Granel G, Gorosito M. Dermoscopic findings in an early malignant fibrous histiocytoma on the face. Dermatol Pract Concept. 2017;7(3):44–6.CrossRef Salerni G, Alonso C, Sanchez-Granel G, Gorosito M. Dermoscopic findings in an early malignant fibrous histiocytoma on the face. Dermatol Pract Concept. 2017;7(3):44–6.CrossRef
24.
go back to reference Arshi A, Sharim J, Park DY, Park HY, Bernthal NM, Yazdanshenas H, Shamie AN. Chondrosarcoma of the osseous spine: an analysis of epidemiology, patient outcomes, and prognostic factors using the SEER registry from 1973 to 2012. Spine (Phila Pa 1976). 2017;42(9):644–52.CrossRef Arshi A, Sharim J, Park DY, Park HY, Bernthal NM, Yazdanshenas H, Shamie AN. Chondrosarcoma of the osseous spine: an analysis of epidemiology, patient outcomes, and prognostic factors using the SEER registry from 1973 to 2012. Spine (Phila Pa 1976). 2017;42(9):644–52.CrossRef
25.
go back to reference Arshi A, Sharim J, Park DY, Park HY, Yazdanshenas H, Bernthal NM, Shamie AN. Prognostic determinants and treatment outcomes analysis of osteosarcoma and Ewing sarcoma of the spine. Spine J. 2017;17(5):645–55.CrossRef Arshi A, Sharim J, Park DY, Park HY, Yazdanshenas H, Bernthal NM, Shamie AN. Prognostic determinants and treatment outcomes analysis of osteosarcoma and Ewing sarcoma of the spine. Spine J. 2017;17(5):645–55.CrossRef
26.
go back to reference Strotman PK, Reif TJ, Kliethermes SA, Sandhu JK, Nystrom LM. Dedifferentiated chondrosarcoma: a survival analysis of 159 cases from the SEER database (2001-2011). J Surg Oncol. 2017;116(2):252–7.CrossRef Strotman PK, Reif TJ, Kliethermes SA, Sandhu JK, Nystrom LM. Dedifferentiated chondrosarcoma: a survival analysis of 159 cases from the SEER database (2001-2011). J Surg Oncol. 2017;116(2):252–7.CrossRef
Metadata
Title
Malignant fibrous neoplasms of long bones: analysis of the surveillance, epidemiology, and end results database from 1973 to 2015
Authors
Yiting Huang
Jianqiao Hong
Jiahong Meng
Haobo Wu
Mingmin Shi
Shigui Yan
Wei Wang
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Musculoskeletal Disorders / Issue 1/2020
Electronic ISSN: 1471-2474
DOI
https://doi.org/10.1186/s12891-019-2971-8

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