ClinConnect ClinConnect Logo
Search / Trial NCT02595255

AMH as a Predictor of Infertility Risk in Children With Cancer (CHANCE)

Launched by ERASME UNIVERSITY HOSPITAL · Nov 2, 2015

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Chemotherapy/Gn Rh (Gonadotropin Releasing Hormone) Analogues/Lymphoma/Children/Fertility

ClinConnect Summary

The CHANCE trial is studying how to identify young girls with cancer who might be at risk of infertility later in life, especially after undergoing treatments like chemotherapy. While many children may go through normal puberty after treatment, some may have a reduced ability to produce eggs, which could lead to difficulties with having children in the future. The goal of this study is to find those girls who seem to develop normally but may still have a lower ovarian reserve, so they can receive specialized follow-up care and, if needed, fertility preservation options.

To be eligible for this trial, girls aged 3 to 14 who have been diagnosed with certain types of cancer and are receiving treatment might participate. This includes those at high risk, like those undergoing bone marrow transplants, as well as those with lower risks who are treated with chemotherapy for conditions such as lymphoma or neuroblastoma. Participants will be monitored closely, and the study aims to provide valuable information about their fertility health, helping doctors make better decisions about their future reproductive options. It's important to note that certain girls with specific medical histories or conditions won't be eligible for this study to ensure their safety.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • * Patients from 3 to 14 year old included - Belong to one of these 3 groups (modified from Wallace et al, 2005):
  • High risk : Conditioning therapy for bone marrow transplantation or pelvic irradiation
  • Moderate/Low risk : Pathologies treated with chemotherapy regimen with moderate or low risk of inducing ovarian function insufficiency: AML, osteosarcoma, Ewing sarcoma, neuroblastoma, non-Hodgkin lymphoma, Hodgkin lymphoma, soft tissue sarcoma, ALL, Wilms tumour, retinoblastoma.
  • No risk (control group) : patients with chronic benign diseases or malignancies who don't receive any chemotherapy or other gonadotoxic treatment.
  • Exclusion Criteria:
  • CNS (central nervous system) irradiation, cerebral tumour
  • Current or previous ovarian disease/surgery
  • Familial history of premature ovarian failure (no iatrogenic or surgical origins)
  • Previous known severe chronic disease potentially affecting normal growth or puberty (diseases inducing malnutrition, anorexia, genetic/congenital disorders as Turner, Kallman, BPES(Blepharophimosis, ptosis, and epicanthus inversus syndrome) syndromes, uncontrolled severe diabetes, Cushing Syndrome, auto-immune diseases, cystic fibrosis, severe renal dysfunction)
  • Genetic/congenital disorders inducing mental retardation

About Erasme University Hospital

Erasme University Hospital, a leading institution in clinical research and patient care, is dedicated to advancing medical knowledge and improving health outcomes through innovative clinical trials. As a prominent academic hospital affiliated with the Université libre de Bruxelles, it combines cutting-edge research with comprehensive clinical services, fostering collaboration among healthcare professionals, researchers, and patients. With a strong emphasis on rigorous scientific methodologies and ethical standards, Erasme University Hospital aims to contribute to the development of new therapies and treatment protocols that address pressing health challenges.

Locations

Lille, , France

Lille, , France

Leuven, , Belgium

Paris, , France

Montegnée, Liège, Belgium

Anvers, , Belgium

Brussels, , Belgium

Brussels, , Belgium

Ghent, , Belgium

Liège, , Belgium

Lille, , France

Montegnée, , Belgium

Patients applied

0 patients applied

Trial Officials

Isabelle Demeestere, PhD

Study Director

Erasme ULB- Belgium

Alina Ferster

Principal Investigator

Queen Fabiola children's university hospital- Belgium

Christine Decanter

Principal Investigator

CHRU Lille, France

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials