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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
Author(s) -
Milano Giuseppe Maria,
Cozza Raffaele,
Ilari Ilaria,
De Sio Luigi,
Boldrini Renata,
Jenkner Alessandro,
De Ioris Maretta,
Inserra Alessandro,
Dominici Carlo,
Donfrancesco Alberto
Publication year - 2006
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.21780
Subject(s) - medicine , etoposide , ifosfamide , vincristine , carboplatin , cyclophosphamide , oncology , regimen , primitive neuroectodermal tumor , sarcoma , ewing's sarcoma , doxorubicin , chemotherapy , surgery , pathology , cisplatin
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. Cancer 2006. © 2006 American Cancer Society.