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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04300179
Other study ID # ESFT_Upp_Egypt
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 7, 2020
Est. completion date December 16, 2020

Study information

Verified date December 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to identify demographic & disease characteristics in pediatric oncology patients diagnosed with Ewing Sarcoma Family of Tumors (ESFT) & treatment outcomes in these patients.


Description:

Ewing sarcoma (ES) and peripheral primitive neuroectodermal tumor (PNET), Both entities that currently comprise the same spectrum of neoplastic diseases known as the Ewing sarcoma family of tumors (EFT), were originally described as distinct clinicopathologic entities. Primitive neuroectodermal tumors (PNETs) first described in 1918 by Stout as a malignant tumor arising from major nerve. Later, in 1921, ES was described as an undifferentiated tumor involving the diaphysis of long bones. It was also reported to arise in soft tissue (extraosseous ES). EFT is aggressive malignant small round cell tumors of bone and soft-tissue that predominantly affecting children and young adults.


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date December 16, 2020
Est. primary completion date December 16, 2020
Accepts healthy volunteers No
Gender All
Age group N/A to 19 Years
Eligibility Inclusion Criteria: - Patients whose age less than 19 years. Patients diagnosed with Ewing Sarcoma Family of Tumors (ESFT). Exclusion Criteria: - Patients whose age more than 19 years. Patients diagnosed with other bone & soft tissue neoplasms.

Study Design


Locations

Country Name City State
Egypt South Egypt Cancer Institute Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival (OS) Participants will be retrospectively followed forward in time from the date of initiation of treatment till death from any cause, an expected average of 5 years From date of treatment initiation until the date of death from any cause or patients censored at last follow up, whichever came first, assessed up to 60 months
Primary Event Free Survival (EFS) Participants will be retrospectively followed forward in time from the date of initiation of treatment till occurrence of an event from any cause (tumor progression, relapse) or death, an expected average of 5 years From date of treatment initiation until the date of event from any cause or patients censored at last follow up, whichever came first, assessed up to 60 months
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