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Long-term Ovarian Fertility in Patients Treated for Lymphoma. (FERTILymph)

U

University Hospital, Lille

Status

Not yet enrolling

Conditions

Lymphoma, Follicular

Study type

Observational

Funder types

Other

Identifiers

NCT05616325
2022_0072
2022-A01753-40 (Other Identifier)

Details and patient eligibility

About

This is an observational, single-center, longitudinal cohort study. In order to evaluate the gonadotoxicity of chemotherapy, an AMH monitoring was initiated in 2006 in our fertility observatory in young patients with lymphoma before, during and after chemotherapy. This study is part of the project "She will get better and then want a child" and is supported by the ARS hauts de France (n° DOS/SDES/AR/FIR/2019/282). Our first study published in 2010 shows that AMH decreases sharply during chemotherapy, regardless of the chemotherapy protocol. At the end of chemotherapy, AMH recovery profiles differ according to the protocol received. This follow-up is therefore essential in order to adapt our practices and our preservation strategies, particularly to the type of chemotherapy. Patients are primarily concerned about their chances of subsequent pregnancy, and there is little evidence in the literature about the impact of chemotherapy on ovarian reserve and long-term fertility.

The fisrt objective of our study is to evaluate, at distance from chemotherapy, the evolution of ovarian function in patients treated for lymphoma by evaluating follicular reserve parameters (AMH and antral follicle count) at 5 and 10 years after the end of chemotherapy compared with the initial workup performed before chemotherapy and the workup performed at 12 months after the end of chemotherapy.

Enrollment

270 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a history of lymphoma treated with chemotherapy
  • followed in the fertility observatory of the Jeanne de Flandre Hospital at the University Hospital of Lille (project "she will heal and then want a child"), who are at least at 5 years since the end of chemotherapy
  • Patients having been informed and having given their written consent to participate in the study.
  • Beneficiary of a social security system.

Exclusion criteria

  • Patient not followed in the fertility observatory.
  • Inability of the patient to undergo the medical follow-up of the trial for geographical, social or psychological reasons.
  • Patient opposed to her participation in the study.
  • Patient under guardianship or curatorship.

Trial contacts and locations

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Central trial contact

Christine DECANTER, MD,PhD; Virginie SIMON, MD

Data sourced from clinicaltrials.gov

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