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Ewing Family of Tumors Treatment (PDQ®)
Patient VersionHealth Professional VersionEn españolLast Modified: 08/18/2008



Purpose of This PDQ Summary






General Information






Cellular Classification






Stage Information






Treatment Option Overview






Ewing Tumor of Bone: Localized Tumors






Ewing Tumor of Bone: Metastatic Tumors






Ewing Tumor of Bone: Recurrent Tumors






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Changes to This Summary (08/18/2008)






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Changes to This Summary (08/18/2008)

The PDQ cancer information summaries are reviewed regularly and updated as new information becomes available. This section describes the latest changes made to this summary as of the date above.

Purpose of This PDQ Summary

Added text about level-of-evidence designations that are intended to help readers assess the strength of the evidence supporting the use of specific interventions or approaches.

General Information

Added text to state that pathologic fractures do not appear to be a prognostic factor for ETB (cited Bramer et al. as reference 11).

Added text to state that positron emission tomogrophy (PET) scans using fluorine-18-fluorodeoxyglucose (FDG) have been shown to provide additional information and have a relevant impact on therapy planning (cited Volker et al. as reference 13).

Stage Information

Added text to state that positron emission tomogrophy (PET) using fluorine-18-fluorodeoxyglucose (FDG) is an optional staging modality (cited Volker et al. as reference 2).

Ewing Tumor of Bone: Localized Tumors

Added Bramer et al. as reference 17.

Added text to state that COG-AEWS07P1 is a pilot clinical trial that is investigating the addition of vincristine, topotecan, and cyclophosphamide (VTC) to a treatment regimen for EFT.

Ewing Tumor of Bone: Metastatic Tumors

Revised text to state that the 6-year event-free survival (EFS) for metastatic disease is approximately 28% (cited Miser et al. as reference 2).

Added text to state that in an Intergroup study, increasing dose intensity of cyclophosphamide, ifosfamide, and doxorubicin did not improve outcome compared with regimens utilizing standard dose intensity, and that this regimen increased toxicity and risk of second malignancy without improving EFS or overall survival.

Revised text to state that, for patients with lung/pleural metastases only, cure rates are approximately 40%.

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