Literature DB >> 25929608

Multimodality Treatment of Pediatric and Adult Patients With Ewing Sarcoma: A Single-institution Experience.

Robert Diaz-Beveridge1, David Lorente, Barbara Torres, Adela Cañete, Esteban Rodrigo, Gema Bruixola, Pablo Berlanga, Encarnacion Reche, Joaquin Montalar, Amparo Verdeguer, Jorge Aparicio.   

Abstract

INTRODUCTION: The treatment of Ewing Sarcoma family of tumors is multimodal, both in children and adults. Axial location and metastases are classic prognostic factors. However, the worse prognosis in older patients is more controversial.
METHODS: Retrospective analysis was performed of pediatric and adult patients treated with the 2001 SEOP protocol: 6 cycles of VIDE chemotherapy (CT). If no progression was observed, local (surgery and/or radiotherapy) and consolidation treatments were performed adjusted to prognosis: 8 cycles of VAC in standard-risk patients or 1 cycle of VAC and high-dose CT and autologous transplant in the case of increased risk.We analyzed induction CT toxicity, type of consolidation treatment, and disease-free (DFS) and overall (OS) survival by the Kaplan-Meier method, with a log-rank analysis of prognostic factors with regard to OS.
RESULTS: Thirty-six patients were analyzed (2003 to 2011). Sixty percent were male, with a median age of 16 years (range, 7 to 57 y). The most frequent location was axial (43%), followed by extremities (34%), extraosseous (18%), and ribs (9%). Fifty-four percent of patients had metastases, of which, 58% were pulmonary.The median follow-up period was 36 months (5 to 101 mo). Median DFS was 25 months (16 to 34 mo) and median OS 29 months (19 to 40 mo), with a 3-year OS of 40%. Median OS from progression was 7 months (0.4 to 15 mo). Age <15 years and normal lactate dehydrogenase levels were associated with prolonged OS.
CONCLUSIONS: Induction CT with the VIDE regimen was feasible in most patients, with a low risk for early progression. Hematological toxicity was substantial but manageable. Adult patients had a worse prognosis. Survival after progression was dismal.

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Mesh:

Year:  2015        PMID: 25929608     DOI: 10.1097/MPH.0000000000000339

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  4 in total

1.  Advantages in Prognosis of Adult Patients with Ewing Sarcoma: 11-years Experiences and Current Treatment Management.

Authors:  Dagmar Adamkova Krakorova; Katerina Kubackova; Ladislav Dusek; Tomas Tomas; Pavel Janicek; Stepan Tucek; Jana Prausova; Igor Kiss; Iva Zambo
Journal:  Pathol Oncol Res       Date:  2017-08-12       Impact factor: 3.201

2.  SERUM VALUES OF ALKALINE PHOSPHATASE AND LACTATE DEHYDROGENASE IN EWING'S SARCOMA.

Authors:  André Mathias Baptista; Juan Pablo Zumárraga; Renan Pires Negrão Dos Santos; Guilherme de Oliveira Haubert; Olavo Pires de Camargo
Journal:  Acta Ortop Bras       Date:  2016 Jul-Aug       Impact factor: 0.513

3.  A Retrospective Multicentric Study of Ewing Sarcoma Family of Tumors in Patients Older Than 50: Management and Outcome.

Authors:  Pauline Rochefort; Antoine Italiano; Valérie Laurence; Nicolas Penel; Audrey Lardy-Cleaud; Olivier Mir; Christine Chevreau; Francois Bertucci; Emmanuelle Bompas; Loic Chaigneau; Dominique Levy; Thomas Ryckewaert; Sarah Dumont; Pierre Meeus; Dominique Ranchere; Jean-Yves Blay; Philippe Alexandre Cassier
Journal:  Sci Rep       Date:  2017-12-20       Impact factor: 4.379

4.  Impact of chemotherapy cycles and intervals on outcomes of nonspinal Ewing sarcoma in adults: a real-world experience.

Authors:  Jianjun Zhang; Yujing Huang; Yuanjue Sun; Aina He; Yan Zhou; Haiyan Hu; Yang Yao; Zan Shen
Journal:  BMC Cancer       Date:  2019-12-02       Impact factor: 4.430

  4 in total

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