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临床试验/NCT05429138
NCT05429138招募中不适用

Ovarian Reserve and Semen Parameters Evolution During Adjuvant Therapy in Melanoma

Assistance Publique Hopitaux De Marseille12 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2022年12月7日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
80
试验地点
12
主要终点
measurement of biological parameters : Anti-Müllerian hormone (AMH) levels in women

研究概览

简要总结

Prospective multicentric study including women aged 18 to 37 and men aged 18 to 45 during their visit to centers for the study and storage of human sperm and eggs (CECOS). Subjects will be included before adjuvant treatment initiation (T0) and immediately after treatment (approximately 1 year after initiation, T1), and, in late post treatment (1 year after treatment cessation, T2).

Expected results: This study will evaluate the evolution of AMH, AFC, and semen parameters in our cohort of melanoma patients treated with anti-PD-1 and targeted therapy in an adjuvant and neoadjuvantsettings.

详细描述

To the best of our knowledge, no data is available in humans on the impact of anti-PD-1 immunotherapies and therapies targeting the MAP kinase pathway, in adjuvant settings, on ovarian reserve and semen quality.

Main objective: to measure pre-treatment (T0) and immediate post-treatment (T1) evolution of anti-Müllerian hormone (AMH) levels reflecting the ovarian reserve in women, and of the total motile sperm count per ejaculate in men, in patients of childbearing age treated with anti-PD-1 immunotherapy or targeted therapies in an adjuvant situation for melanoma at high risk of recurrence.

Method: Prospective multicentric study including women aged 18 to 37 and men aged 18 to 45 during their visit to centers for the study and storage of human sperm and eggs (CECOS). Subjects will be included before adjuvant treatment initiation (T0) and immediately after treatment (approximately 1 year after initiation, T1), and, in late post treatment (1 year after treatment cessation, T2).

At each of their visit to CECOS (T0, T1 and T2), the women will have an AMH assay and an antral follicle count (AFC) by ultrasound while the men will perform a semen analysis (count, spermocytogram and staining with aniline blue for analysis of chromatin condensation).

A standardized questionnaire aimed at collecting data about factors that may alter fertility will be submitted at each of these visits.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have provided a signed, dated and written consent prior to any specific procedures, sampling and analyses
  • Patients with valide Health Inssurance Scheme
  • Female between 18 and 37 years old and male between 18 and 45 years old
  • During the 2 months before the introduction of an approved regimen of adjuvant anti-PD-1 immunotherapy or neoadjuvant plus adjuvant or targeted therapy for an high-risk of reccurence melanoma
  • Adjuvant or neoadjuvant plus adjuvant treatment must be prescribed as part of routine care

排除标准

  • Individuals deprived of liberty or placed under the authority of a tutor
  • Patients unable to understand, read and/or sign an informed consent
  • History of cytotoxic treatment before T0 that can alterate the studied parameters
  • In male, totale motile sperm count per ejaculate inferior to 39 millions at T0
  • In women, an age-specific AMH level inferior to the 10th percentile at T0
  • Any condition which in the Investigator's opinion would jeopardize compliance with the protocol of the study
  • Patients that will received an investigational treatment during the study timeframe (an observational research is allowed)
  • Patients who have changed the type of adjuvant treatment during adjuvant treatment (targeted switch therapy versus targeted immunotherapy and vice versa) or after the neoadjuvant phase due to the pathological response obtained.

结局指标

主要结局

measurement of biological parameters : Anti-Müllerian hormone (AMH) levels in women

时间窗: T1 (=Day0 + 12 months)

change in Anti-Müllerian hormone (AMH) levels in women

measurement of biological parameters : Change in sperm motility count in men

时间窗: T1 (=Day0 + 12 months)

Change in sperm motility count per ejaculate in men

次要结局

  • measurement of biological parameters : levels of spermatozoids with sperm chromatin abnormalities(T0 = Day 0 = treatment initiation; T1 = Day0 + 12 months; T2 = T1 + 12 months.)
  • measurement of biological parameters : Change in sperm count(T0 = Day 0 = treatment initiation; T1 = Day0 + 12 months; T2 = T1 + 12 months.)
  • measurement of biological parameters : Change in sperm motility count(T0 = Day 0 = treatment initiation; T1 = Day0 + 12 months; T2 = T1 + 12 months.)
  • measurement of biological parameters : Antral follicle count in women(T0 = Day 0 = treatment initiation; T1 = Day0 + 12 months; T2 = T1 + 12 months.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (12)

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