Asian Pacific Journal of Cancer Prevention

  • 제15권1호
  • /
  • Pages.327-330
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  • 2014
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  • 1513-7368(pISSN)
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  • 2476-762X(eISSN)
아시아태평양암예방학회 (Asian Pacific Journal of Cancer Prevention)
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Treatment and Outcomes of Ewing Sarcoma in Turkish Adults: A Single Centre Experience

  • Seker, Mehmet Metin (Department of Medical Oncology, Cumhuriyet University Medical Faculty) ;
  • Kos, Tugba (Department of Medical Oncology, Manisa State Hospital) ;
  • Ozdemir, Nuriye (Department of Medical Oncology, Numune Education and Research Hospital) ;
  • Seker, Ayse (Department of Medical Oncology, Mutki State Hospital) ;
  • Aksoy, Sercan (Department of Medical Oncology, Hacettepe University Cancer Institute) ;
  • Uncu, Dogan (Department of Medical Oncology, Numune Education and Research Hospital) ;
  • Zengin, Nurullah (Department of Medical Oncology, Numune Education and Research Hospital)
  • 발행 : 2014.01.15
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초록

Background: Ewing sarcoma is a small round cell tumor arising from soft tissue and bone that predominantly affects children and adolescents. The most unfavorable prognostic factor is the presence of distant metastasis at the time of diagnosis. Materials and Methods: The records of 26 Ewing sarcoma patients (14 male, 12 female) were re-evaluated retrospectively. Results: The median age was 26.5 (19-42) years. Eight patients (31%) showed a primary tumor in their extremities, 8 (31%) in the thorax, 4 (15%) at the vertebra, 4 (15%) in the head and neck, and 2 (8%) in the abdomen. Five patients (19%) had distant metastasis at diagnosis. The median progression-free survival was 72 months and 10 months in localized and metastatic disease, respectively (p=0.005). The overall survival rate was 19 months in metastatic disease, and the 5-year overall survival rate was 64% in localized disease (p=0.006). Patients who had localized disease in the extremities and were under age 30 had a favorable prognosis. Conclusions: Although Ewing sarcoma is a tumor affecting children and adolescents, it may be seen in adults, where the prognosis is generally worse. Although it is a highly malignant tumor, it is possible to achieve improved survival with combined modality treatments.

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참고문헌

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  3. Prognosis and Outcome of Adult Patients with Ewing Sarcoma (Local Experience) vol.08, pp.08, 2017, https://doi.org/10.4236/jct.2017.88066