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Long-term Ovarian Fertility in Patients Treated for Lymphoma.

Not yet recruiting
Conditions
Lymphoma, Follicular
Registration Number
NCT05616325
Lead Sponsor
University Hospital, Lille
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
270
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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Follicular reserve parameters (AMH and antral follicle count)at the end of chemotherapy

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

Secondary Outcome Measures
NameTimeMethod
Scores Mood (PHQ)at 5 and 10 years after the end of chemotherapy.
Scores on the Reproductive Concerns (RCACS)at 5 and 10 years after the end of chemotherapy.
Life Satisfaction (SWLS) scalesat 5 and 10 years after the end of chemotherapy.
Cumulative incidence of pregnancy at 5 years and 10 years from the end of treatment defined by the achievement of at least one spontaneous or induced pregnancy.at 5 and 10 years after the end of chemotherapy.
Rate of miscarriages, ectopic pregnancies, and live births (single, multiple)at 5 and 10 years after the end of chemotherapy.

defined by the ratio of the number of miscarriages, ectopic pregnancies, and live births to the number of pregnancies obtained by ART (with or without reuse of gametes or frozen ovarian tissue).

Pregnancy rate obtained by ART (with or without gamete reuse)at 5 and 10 years after the end of chemotherapy.

defined by the ratio between the number of clinical pregnancies and the number of ART attempts performed (with or without gamete reuse or frozen ovarian tissue).

Quality of Life (FACT-G7)at 5 and 10 years after the end of chemotherapy.
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