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Tural, D., Molinas Mandel, N., Dervisoglu, S., Oner Dincbas, F., Koca, S., Colpan Oksuz, D., Kantarci, F., Turna, H., Selcukbiricik, F. and Hiz, M. (2012) Extraskeletal Ewing’s Sarcoma Family of Tumors in Adults: Prognostic Factors and Clinical Outcome. Japanese Journal of Clinical Oncology, 42, 420-426.
https://doi.org/10.1093/jjco/hys027
has been cited by the following article:
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TITLE:
Prognosis and Outcome of Adult Patients with Ewing Sarcoma (Local Experience)
AUTHORS:
Mohamed Ashour, Salem Al Shammari, Hanan Shafik, Ahmed Mohialdien
KEYWORDS:
Adult, Ewing, Sarcoma, Treatment
JOURNAL NAME:
Journal of Cancer Therapy,
Vol.8 No.8,
August
8,
2017
ABSTRACT:
Objective: Aim of this work is to assess clinical features, outcome and prognosis
of adult patients diagnosed with Ewing Sarcoma (ES). Patients, Methods
and Results: The records of 53 adult patients treated with Euro-Ewing
protocol at Kuwait cancer control center (KCCC) over a period of 5 years
were reviewed. Mean age was 26.9 ± 1.25 years. Thirty percent of patients
presented with metastatic disease, and 65% of tumors were centrally located
and 50% were ≥ 8 cm. All patients received initially VIDE protocol. 13.5%
achieved complete remission (CR), and 57.7% achieved partial response (PR).
Approximately 1/3 of patients underwent surgery which was adequate in 76%
of them, and all patients received local radiotherapy. Post local treatment 56%
of patients received VAC and 44% received VAI protocol. Mean treatment
duration was 11 months ± 0.54. Median follow-up duration was 38.39 (33.49 -
43.28) months At the end of follow up 20% of patients relapsed locally and
36% distally. Median PFS was 46.9 months (95% CI 41.42 - 52.39), Median OS
was 55.43 ms (95% CI 30.71 - 75.74); survivals at 3 and 5 years were 88%, 46%
respectively. Conclusion: In this series metastases at presentation and wide
surgical margins were the most important prognostic factors. Multimodality
therapy is necessary for this rare disease.