Literature DB >> 17401006

Extraosseous localized ewing tumors: improved outcome with anthracyclines--the French society of pediatric oncology and international society of pediatric oncology.

Marie-Pierre Castex1, Hervé Rubie, Michael C G Stevens, Carlota Calvo Escribano, Jérôme Sales de Gauzy, Anne Gomez-Brouchet, Annie Rey, Olivier Delattre, Odile Oberlin.   

Abstract

PURPOSE: To evaluate the outcome of children with an extraosseous Ewing tumor (EOE) according to treatment. PATIENTS AND METHODS: Children with EOE were treated either with the strategy used for malignant mesenchymal tumors (MMTs) by the International Society of Pediatric Oncology (SIOP) or with the French Society of Pediatric Oncology (SFOP) regimen used for osseous Ewing tumors (OET). The MMT strategy included vincristine/actinomycin for small and resected tumors or ifosfamide/vincristine/actinomycin for unfavorable sites or unresectable tumors. Surgical excision was to be attempted after four courses, followed by local irradiation in case of residue. Osseous Ewing (OE) protocol included three courses of cyclophosphamide/doxorubicin followed either by two similar courses in case of good response or two courses of ifosfamide/etoposide in case of no response. After resection of the primary, treatment included conventional chemotherapy in case of good histologic response and high-dose chemotherapy and radiotherapy for poor response. All diagnosis specimens were reviewed by the panel.
RESULTS: Between 1989 and 1999, 63 patients were registered. Characteristics of patients treated by both protocols were similar. Five-year overall survival (OS) and event-free survival (EFS) of those treated with the OE protocol are 83% and 75%, respectively, which is significantly better than the OS and EFS of those treated with the MMT strategy (59% and 44%, respectively; P = .04 and .008, respectively). The size of the primary and the type of protocol influenced patients' EFS. In multivariate analysis, only the regimen had an impact on OS and EFS.
CONCLUSION: Our study shows that patients with EOE should be treated with OE regimens, probably because of the use of anthracyclines.

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Year:  2007        PMID: 17401006     DOI: 10.1200/JCO.2005.05.0559

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  19 in total

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Review 2.  Ewing sarcoma/peripheral primitive neuroectodermal tumor and related tumors.

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3.  Evaluating the Soft Tissue Sarcoma Paradigm for the Local Management of Extraskeletal Ewing Sarcoma.

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Journal:  Oncologist       Date:  2020-12-14

4.  Clinical features and outcomes in patients with extraskeletal Ewing sarcoma.

Authors:  Mark A Applebaum; Jennifer Worch; Katherine K Matthay; Robert Goldsby; John Neuhaus; Daniel C West; Steven G Dubois
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5.  Treatment of adult patients with Ewing's sarcoma: compliance with chemotherapy protocols & toxicity.

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Review 6.  Extraosseous Ewing Sarcoma: Diagnosis, Prognosis and Optimal Management.

Authors:  George Galyfos; Georgios A Karantzikos; Nikolaos Kavouras; Argiri Sianou; Konstantinos Palogos; Konstantinos Filis
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7.  Dose-intensified compared with standard chemotherapy for nonmetastatic Ewing sarcoma family of tumors: a Children's Oncology Group Study.

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Journal:  J Clin Oncol       Date:  2009-04-06       Impact factor: 44.544

8.  Extraskeletal Ewing sarcoma in children and adolescents: impact of narrow but negative surgical margin.

Authors:  Sajid S Qureshi; Siddharth Laskar; Seema Kembhavi; Sanjay Talole; Girish Chinnaswamy; Tushar Vora; Mukta Ramadwar; Saral Desai; Nehal Khanna; Mary Ann Muckaden; Purna Kurkure
Journal:  Pediatr Surg Int       Date:  2013-08-28       Impact factor: 1.827

9.  Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group.

Authors:  Thomas Cash; Elizabeth McIlvaine; Mark D Krailo; Stephen L Lessnick; Elizabeth R Lawlor; Nadia Laack; Joel Sorger; Neyssa Marina; Holcombe E Grier; Linda Granowetter; Richard B Womer; Steven G DuBois
Journal:  Pediatr Blood Cancer       Date:  2016-06-14       Impact factor: 3.167

Review 10.  Current management of pediatric soft tissue sarcomas.

Authors:  Surasak Sangkhathat
Journal:  World J Clin Pediatr       Date:  2015-11-08
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