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New Approaches Promise to Improve Local Ewing Sarcoma Results.
Cohen, Ian J; Ash, Shifra.
Afiliação
  • Cohen IJ; Rina Zaizov Department of Pediatric Hematology­Oncology, Schneider Children's Medical Center of Israel, Petach Tikva.
  • Ash S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv.
J Pediatr Hematol Oncol ; 44(6): 280-284, 2022 08 01.
Article em En | MEDLINE | ID: mdl-35537008
ABSTRACT
The study by Whelan and colleagues showed that addition of busulfan and melphalan conditioning and autologous stem cell rescue to conventional EURO-E.W.I.N.G STUDY chemotherapy in local nonmetastatic Ewing sarcoma improves prognosis. However, almost 30% of these study patients will have relapsed before this stage of therapy is reached, and 78% of his patients were at high risk because of inadequate response to the initial chemotherapy given. Further improvement could be achieved by the integration of other novel advances with this approach. Ash and colleagues have shown that the separation of such cases into high- and low-risk groups by using CD56 negativity of the tumor cells is an improvement over current methods with a 100% 10-year progression-free survival in CD56- nonpelvic local isolated Ewing sarcoma patients. Their patients were treated on the SCMCIE 94 protocol, associated with no relapses before 30 months in 24 consecutive patients independent of the CD status. Integration of these novel approaches in diagnosis and treatment would allow truly high-risk patients, who would benefit from the procedure, to reach the busulfan and melphalan stage of therapy and delineate those patients who can be cured without such therapy. Details of the SCMCIE 94 protocol are given and the possible reasons for the different relapse patterns are discussed.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Neoplasias Ósseas Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Neoplasias Ósseas Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article