Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Dec 23:24:9370-9375.
doi: 10.12659/MSM.911882.

Clinical Features and Prognostic Factors in Elderly Ewing Sarcoma Patients

Affiliations

Clinical Features and Prognostic Factors in Elderly Ewing Sarcoma Patients

Hua-Fei Liu et al. Med Sci Monit. .

Abstract

BACKGROUND Elderly patients with Ewing sarcoma have a very poor prognosis, and treatment remains a challenge. However, the outcomes and potential prognostic factors of elderly Ewing sarcoma patients are rarely documented. Therefore, we investigated the prognosis of this special cohort and determine independent prognostic factors. MATERIAL AND METHODS A cohort of Ewing sarcoma patients aged over 40 years from 1973 to 2015 was identified from the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) database. The Kaplan-Meier method and a Cox proportional hazard regression model were used for the prognostic analysis. RESULTS A total of 162 patients were included with a mean age of 53 years. The 5-year overall survival (OS) and cancer-specific survival (CSS) rates of the entire group were 43.7% and 47.9%, respectively. The sex, location, tumor size, and radiation treatment had no effect on survival outcomes on univariate analysis. Tumor stage, surgery, and chemotherapy were significant indicators of both OS and CSS on multivariable analysis. CONCLUSIONS Surgery in combination with chemotherapy had a significant survival benefit in elderly Ewing sarcoma patients and should be recommended.

PubMed Disclaimer

Conflict of interest statement

Conflicts of interest

None.

Figures

Figure 1
Figure 1
Flow chart for selection of the study population. SEER – surveillance, epidemiology, and end results; ICD-O-3 – international classification of diseases for oncology, 3rd edition; ES – Ewing sarcoma.
Figure 2
Figure 2
Kaplan-Meier method estimated OS in elderly patients with Ewing sarcoma of bone stratified by: (A) tumor stage, (B) surgery, and (C) chemotherapy.
Figure 3
Figure 3
Kaplan-Meier method estimated CSS in elderly patients with Ewing sarcoma of bone stratified by: (A) tumor stage, (B) surgery, and (C) chemotherapy.

References

    1. Cotterill SJ, Parker L, Malcolm AJ, et al. Incidence and survival for cancer in children and young adults in the North of England, 1968–1995: A report from the Northern Region Young Persons’ Malignant Disease Registry. Br J Cancer. 2000;83:397–403. - PMC - PubMed
    1. Maheshwari AV, Cheng EY. Ewing sarcoma family of tumors. J Am Acad Orthop Surg. 2010;18:94–107. - PubMed
    1. Dunst J, Schuck A. Role of radiotherapy in Ewing tumors. Pediatric Blood Cancer. 2004;42:465–70. - PubMed
    1. Duchman KR, Gao Y, Miller BJ. Prognostic factors for survival in patients with Ewing’s sarcoma using the surveillance, epidemiology, and end results (SEER) program database. Cancer Epidemiol. 2015;39:189–95. - PubMed
    1. Wan ZH, Huang ZH, Chen LB. Survival outcome among patients with Ewing’s sarcoma of bones and joints: A population-based cohort study. Sao Paulo Med J. 2017;136(2):116–22. - PMC - PubMed