High histologic and overall response to dose intensification of ifosfamide, carboplatin, and etoposide with cyclophosphamide, doxorubicin, and vincristine in patients with high-risk Ewing sarcoma family tumors: The Bambino Gesù Children's Hospital experience

Giuseppe Maria Milano, Raffaele Cozza, Maria Ilari, Luigi De Sio, Renata Boldrini, Alessandro Jenkner, Maretta De Ioris, Alessandro Inserra, Carlo Dominici, Alberto Donfrancesco

Research output: Contribution to journalArticle

Abstract

BACKGROUND. Ewing sarcoma (ES) and extraosseous ES/primitive neuroectodermal tumors (PNET) share histopathologic features of the ES family of tumors (ESFT). The authors report on their results from a regimen of ifosfamide, carboplatin, and etoposide (ICE) with cyclophosphamide, doxorubicin, and vincristine (CAV) dose intensification in patients with high-risk ESFT. METHODS. Since 1990, patients with ESFT and with 1 or more of the following risk factors were reviewed: tumor volume > 200 mL, tumor site with a poor prognosis, and pulmonary and/or bone marrow metastases. RESULTS. Thirty-six patients with ESFT who were involved in the study were divided into 2 arms of 18 patients each. One group received treatment with various regimens, and the other group received treatment with ICE plus CAV. The disease was brought under control more rapidly in the latter patients, for whom surgery was more easily feasible, and up to 90% of patients achieved a major response, with an estimated 3-year overall survival rate of 67% ± 12%. CONCLUSIONS. The current results showed that ICE plus CAV was tolerated well and was effective in the studied subset of tumors, indicating that dose intensification correlates with better disease control, a high percentage of necrosis, and conservative surgery in patients with high-risk ESFT.

Original languageEnglish
Pages (from-to)1838-1845
Number of pages8
JournalCancer
Volume106
Issue number8
DOIs
Publication statusPublished - May 15 2006

Keywords

  • Chemotherapy
  • Dose intensification
  • Ewing sarcoma family tumors
  • Histologic Response
  • Survival
  • Tumor necrosis

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

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