Literature DB >> 15726621

Favorable outcome of Ewing sarcoma family tumors to multiagent intensive preoperative chemotherapy: a single institution experience.

Maria Moschovi1, Georgios Trimis, Kalliopi Stefanaki, John Anastasopoulos, Vassiliki Syriopoulou, Eleutheria Koultouki, Fotini Tzortzatou-Stathopoulou.   

Abstract

BACKGROUND: Aim of our study was to evaluate the efficacy of multiagent intensive preoperative chemotherapy in patients with Ewing sarcoma family tumors (ESFT), in order to succeed a better percentage of necrosis before surgical resection. PROCEDURE: Eighteen patients with ESFT were treated with the same multiagent intensive preoperative protocol. 5/18 patients had bone Ewings sarcoma (EWS) and 13/18 had peripheral primitive neuroectodermal tumor (PNET). None had metastases at diagnosis. Chemotherapy consisted of 5 or 6 cycles with vincristine, cisplatin, cyclophosphamide, and Adriamycin, followed by 12 cycles of vincristine, cyclophosphamide, and actinomycin-D. Five patients with EWS underwent total resection after 5-6 cycles of preoperative chemotherapy and prosthetic replacement was performed in two of them. In 3/13 patients with PNET the tumor was resected at diagnosis and in 1/13 after 5 cycles of chemotherapy, while 9/13 patients received chemotherapy only and/or radiotherapy.
RESULTS: In patients with EWS, the histologic specimens of the resected tumors showed that tissue necrosis was 100% in four patients and 95% in one patient. The good histologic response reflects the effectiveness of this regimen in all ESFT. No patient had topical recurrence or developed metastatic disease during follow-up period (2-13 years, mean time 7.4 years). All patients had the scheduled cycles without delays or dose reductions. There were no major side effects of chemotherapy.
CONCLUSIONS: The intensive chemotherapy schedule, comprising of 5-6 cycles preoperatively, seems to maximize the percentage of tumor necrosis, thus improving outcome. Our study implies that this combined therapy may improve the prognosis of ESFT. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15726621     DOI: 10.1002/jso.20206

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  6 in total

1.  Cranial Ewing's sarcoma in children.

Authors:  Maria Moschovi; George A Alexiou; Natalia Tourkantoni; Mirsini-Ersi Balafouta; Christos Antypas; Maria Tsiotra; George Sfakianos; Neofytos Prodromou
Journal:  Neurol Sci       Date:  2011-03-02       Impact factor: 3.307

2.  Solitary epidural brain metastasis of a peripheral neuroepithelioma (a primitive neuroectodermal tumor): a case report.

Authors:  Atoosa Adibi; Roozbeh Barikbin; Navid Koleini; Maryam Farghadani; Kourosh Mougouei; Farnaz Farshidfar
Journal:  J Radiol Case Rep       Date:  2008-07-01

3.  Huge primitive neuroectodermal tumor of the pancreas: report of a case and review of the literature.

Authors:  Thilo Welsch; Gunhild Mechtersheimer; Sebastian Aulmann; Sascha A Mueller; Markus W Buechler; Jan Schmidt; Peter Kienle
Journal:  World J Gastroenterol       Date:  2006-10-07       Impact factor: 5.742

4.  Primitive Neuroectodermal Tumor of the Pancreas: A Case Report and Review of the Literature.

Authors:  Uirá Teixeira; Marcos Goldoni; Michelle Unterleider; João Diedrich; Diogo Balbinot; Pablo Rodrigues; Rodolfo Monteiro; Daniel Gomes; José Sampaio; Paulo Fontes; Fábio Waechter
Journal:  Case Rep Surg       Date:  2015-05-26

Review 5.  [Giant primitive nuroectodermal tumor of mediastinum: a case report with literature review].

Authors:  Zhiqiang Wu; Hongli Wan; Min Shi; Wei Gao; Zhanpeng Wang; Huiping Liu; Qingxin Li
Journal:  Zhongguo Fei Ai Za Zhi       Date:  2013-05

6.  Outcome of multidisciplinary treatment of peripheral primitive neuroectodermal tumor.

Authors:  Yidi Liu; Yan Yuan; Fuquan Zhang; Ke Hu; Jie Qiu; Xiaorong Hou; Junfang Yan; Xin Lian; Shuai Sun; Zhikai Liu; Jie Shen
Journal:  Sci Rep       Date:  2020-09-24       Impact factor: 4.379

  6 in total

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