FEED 研究中的雄性交配前处理:长度并不代表一切。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-08-28 DOI:10.1016/j.reprotox.2024.108703
Paul Barrow
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引用次数: 0

摘要

ICH S5(R3)指南建议,在 FEED 研究中,雄性啮齿动物在交配前接受治疗的时间应≥2 周,但这一时间常常被批评为太短,无法检测对精子成熟、交配行为和雄性生育能力的所有影响。在 FEED 研究中,男性一般会在开始同居后持续≥5 周。本综述确定了 2022 年和 2023 年 FDA 批准的新药 FEED 研究中男性 2 周交配前治疗期的使用频率。44 种药物规定了男性交配前治疗期。其中只有 16% 的药物有 2 周的男性交配前治疗期。52%的药物为 4 周。在文献中没有发现使用 4 周而不是 2 周的交配前处理期可以检测到雄性介导的生殖毒性的药物实例。在计划进行 FEED 研究之前,通常要完成在 2 个物种中进行的重复剂量研究,其治疗时间至少与患者的治疗时间相当。如果在重复剂量研究中未检测到对雄性生殖器官的影响,2 周的交配前治疗期似乎足以检测出对雄性交配能力的影响。如果在重复剂量研究中发现了对精子发生的毒性影响,则雄性 FEED 研究对监管的作用不大。即使在 FEED 研究中没有发现对交配能力和生育能力的影响,与药物有关的精子发生障碍也可能被认为与人类有关。
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Male premating treatment in FEED studies: Length is not everything

The ICH S5(R3) guideline recommends that male rodents in a FEED study are treated for ≥2 weeks before mating, which has frequently been criticized as being too short for the detection of all effects on sperm maturation, mating behavior and male fertility. In a FEED study, males generally continue for ≥5 weeks after the start of cohabitation. This review determines how often a 2-week premating treatment period for males was used in FEED studies of novel drugs approved by the FDA in 2022 and 2023. The male premating treatment duration was specified for 44 drugs. Only 16 % of these had a 2-week male premating treatment period. 52 % of drugs had a 4-week period. No examples were found in the literature of drugs for which male-mediated reproductive toxicity could have been detected using a 4-week, but not a 2-week, premating treatment period. Repeat dose studies in 2 species, with a duration of treatment at least equivalent to that in patients, are generally completed before the FEED study is planned. Providing no effects on male reproductive organs are detected in the repeat dose studies, a 2-week premating treatment period appears sufficient for the detection of effects on male mating performance. If toxic effects on spermatogenesis are detected in the repeat dose studies, a male FEED study serves little regulatory purpose. Even in the absence of effects on mating performance and fertility in the FEED study, a drug-related disruption of spermatogenesis would likely be considered pertinent to the human.

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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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