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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05107843
Other study ID # 7715
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date December 31, 2021

Study information

Verified date October 2021
Source University Hospital, Strasbourg, France
Contact Natacha ENTZ-WERLE, MD, PhD
Phone 33.3.88.12.80.96
Email Natacha.Entz-Werle@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this pilot study is therefore to retrospectively measure the volume and percentage of necrosis on diagnostic MRI in T1 sequence and in parallel to study the expression of immunohistochemical markers of hypoxia (HIF-1α, CAIX , HIF-2α, pS6, phosphomTor, CD163 and CD68) on diagnostic biopsies of high-grade osteosarcomas from 2007 to 2018 in the Strasbourg center, focusing on the pediatric population. The investigators will systematically carry out a correlation analysis between these different parameters and with the clinical data of these same patients (response to chemotherapy, presence of metastases or not and overall and recurrence-free survival). This will eventually make it possible to highlight new prognostic markers at diagnosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers
Gender All
Age group 1 Year to 20 Years
Eligibility Inclusion Criteria: - Subject = 20 years at diagnosis - Subject having been treated for osteosarcoma in the OS2006 protocol or treated according to - Supported at Strasbourg University Hospitals between 05/01/2007 and 10/31/2018 - Availability of its diagnostic tumor material stored in paraffin - having an MRI diagnostic evaluation comprising the injected T1 sequences necessary for the analysis of the volume / necrotic proportion. Exclusion Criteria: - Opposition of the patient (or his legal representatives if he is a minor) to participate in the study - Diagnosis other than osteosarcoma - Biological tissue from a patient who does not meet all the inclusion criteria - Patient under legal protection - Patient under guardianship or guardianship

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service Pédiatrie Onco-hématologie - Pédiatrie III - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retropsective study of pediatric osteosarcomas Files analysed retrospectively from January 01, 2007 to December 31, 2018 will be examined]
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