MedPath

Dinutuximab Beta at the HUS and the Toulouse Oncopole

Recruiting
Conditions
Neuroblastoma
Registration Number
NCT06275334
Lead Sponsor
University Hospital, Strasbourg, France
Brief Summary

In this study the investigators wish to describe the cohort of pediatric patients suffering from neuroblastoma and treated with Dinutuximab and to compare the costs and quality of life between the two French centers, the University Hospital of Strasbourg (HUS) and the Oncopole of Toulouse.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Subjects aged 2 years to 25 years
  • Male or female gender
  • Subjects suffering from neuroblastoma and treated at the HUS or at the Oncopole center in Toulouse during the period from January 1, 1998 to December 31, 2023.
  • Subject (and/or holders of parental authority) not opposing, after information, the reuse of the child's data for the purposes of this research and agreeing to respond to the quality of life survey.
Exclusion Criteria
  • Patient or parents of the minor having expressed their opposition to participating in the study.
  • specific clinical forms of the disease,
  • interfering treatments and associated diseases.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of two methods of treating a pediatric pathology in two French health establishments, the HUS and the Oncopole of Toulouse.The period concerned is from January 1, 1998 to December 31, 2023.

This study is retrospective and consists of comparing two methods of treating neuroblastoma in two health establishments and covers the period from January 1, 1998 to December 31, 2023.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Service de Pharmacie - Stérilisation - CHU de Strasbourg - France

🇫🇷

Strasbourg, France

© Copyright 2025. All Rights Reserved by MedPath