Abstract
Objective: To survey on the clinical and paraclinical characteristics of Ewing's sarcoma at Oncology Hospital HCMC. Evaluate the outcome, side effects of the treatment regimen and the overall survival. Patients and methods: 19 patients s 16 years-old were diagnosed with Ewing's Sarcoma based on anapathology and immunohistochemistry. All of patients were treated at Oncology Hospital HCMC from 1/2009 to 12/2013. Results: The median age was 7.5 years (range 4 months old to 15 years old). Boy have a higher risk than girl, the proportion of male/female was 5.3/1. After initial symptoms, time to clinical diagnosis was 3.5 months. Primary tumors of bone accounted for 42.1%, 57.9% outside the bone, in which the majority of tumors in the limbs (47.4%), head and neck (21%), spinal cord (15.8%), other (15.9%). Ewing's sarcoma histological type (57.9%) 78.9% response chemotherapy in which complete response was 26,3%. Progression diseases or metastases after chemotherapy were relatively high (21.1%). The proportion of 2-year overall survival and 3-year overall survival were 33.1% and 56.3%. Conclusion: Primary tumors resection is an important factor to affect the outcome of treatment adjuvant (chemotherapy and radiotherapy). There is no difference in the level of response to chemotherapy factors such as: type of chemotherapy regimen, initial surgical approach, age group. Adjuvant radiation therapy improves local control after resection and chemotherapy. Several factors could adversely affect the outcome of survival, including: metastasis condition, the level of response to chemotherapy and radiotherapy.
References
Aparicio J., Munarizz B., Pastor M. (1998), Long-term follow up and prognostic factors in Ewing's sarcoma: a multivariate analysis of 116 patients from a single institution, Oncology, 55:20-26.
Hai-Tao Tao, Yi Hu, Jin-Liang Wang, et al (2005), Extraskeletal Ewing Sarcomas in Late Adolescence and Adults: A Study of 37 Patients., Asian Pacific J Cancer Prev, 14(5): 2967-2971.
Abha A. Gupta, Alberto Pappo, Natasha Saunders, et al. (2010), Clinical outcome of children and adults with localized Ewing sarcoma, Cancer, 10:3189-3194.
Pan C., Tang JY., Xue HL., et al. (2009), Clinical report on diagnosis and treatment of 14 cases with pediatric Ewing's sarcoma family tumors, Zhonghua Er Ke Za Zhi, 47(3): 179-182.
Joe Lee, Bang H. Hoang, Argyrios Ziogas, et al. (2010), Analysis of Prognostic Factors in Ewing Sarcoma Using a Population-Based Cancer Registry, Cancer, 15: 1964-1973.
Ladenstein R., Pötschger U., Le Deley MC., et al. (2010), Primary disseminated multifocal Ewing sarcoma: results of the Euro-EWING 99 trial, J Clin Oncol, 28(20): 3284-3291.
Ferrari S., Palmerini E., Alberghini M., et al. (2010), Vincristine, doxorubicin, cyclophosfamide, actinomycin D, ifosfamide, and etoposide in adult and pediatric patients with nonmetastatic Ewing sarcoma. Final results of a monoinstitutional study, Tumori, 96(2): 213-218.
Lee JA., Kim DH., Cho J., et al. (2011), Treatment outcome of Korean patients with localized Ewing sarcoma family of tumors: a single institution experience, Jpn J Clin Oncol, 41(6): 776-782.
Published | 03-03-2025 | |
Fulltext |
|
|
Language |
|
|
Issue | No. 28 (2015) | |
Section | Original article | |
DOI | ||
Keywords | Sarcôm Ewing Ewing's sarcoma. |

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Copyright (c) 2025 Journal of Clinical Medicine Hue Central Hospital