Cigni Alessandro, Faedda Rossana, Atzeni Maria Maddalena, Pileri Piera Veronica, Alagna Sergio, Rovasio Pierpaolo, Satta Andrea Ercole, Loi Maria Rita, Sini Annalisa, Satta Vincenzo, Masala Antonio
Department of Internal Medicine, University of Sassari, Sassari, Italy.
Am J Kidney Dis. 2008 Nov;52(5):887-96. doi: 10.1053/j.ajkd.2008.06.017.
Prepubertal patients receiving chemotherapy are relatively resistant to cyclophosphamide-induced germinal cell alterations. We studied the possible protective effect of testosterone and triptorelin to inhibit gonadal activity in men and women receiving cyclophosphamide, respectively.
Nonrandomized trial.
SETTING & PARTICIPANTS: 28 consecutive patients, 11 men and 17 women, from a university medical center with various forms of glomerulonephritis, treated with cyclophosphamide.
Men received cyclophosphamide plus testosterone; women were divided into 2 groups: 13 patients (group A) received cyclophosphamide plus triptorelin; 4 (group B) received only cyclophosphamide.
OUTCOMES & MEASUREMENTS: Serum follicle-stimulating hormone (FSH) and serum luteinizing hormone levels and, in addition, sperm counts and testosterone levels in men and estradiol levels in women were measured before and after treatment with cyclophosphamide.
All 10 men became azoospermic or severely oligospermic during treatment; after 12 months, all except 1 had a normal sperm count and FSH levels were normal. In women during cyclophosphamide therapy, amenorrhea occurred in all patients. After cessation of therapy, all women in group A started to menstruate regularly, and at the end of follow-up, ovulatory cycles were demonstrated in all women. Hormone levels showed no significant changes throughout the observation period. Six women conceived, and the pregnancies were brought to term successfully without complications. In group B, all 4 women developed sustained amenorrhea; serum FSH and luteinizing hormone levels at the end of therapy and follow-up were significantly higher with respect to baseline; estradiol levels at the end of follow-up were significantly lower compared with baseline and corresponding values in group A.
The substudy in men is uncontrolled, the substudy in women is nonrandomized.
The study suggests a protective effect of testosterone and triptorelin against cyclophosphamide-induced gonadal damage in men and women with various forms of kidney disease, respectively.
青春期前接受化疗的患者对环磷酰胺诱导的生殖细胞改变相对耐药。我们分别研究了睾酮和曲普瑞林对接受环磷酰胺治疗的男性和女性抑制性腺活动的可能保护作用。
非随机试验。
来自一所大学医学中心的28例连续患者,其中11例男性和17例女性,患有各种形式的肾小球肾炎,接受环磷酰胺治疗。
男性接受环磷酰胺加睾酮治疗;女性分为两组:13例患者(A组)接受环磷酰胺加曲普瑞林治疗;4例(B组)仅接受环磷酰胺治疗。
在环磷酰胺治疗前后,测量血清促卵泡生成素(FSH)和血清黄体生成素水平,此外,还测量男性的精子计数和睾酮水平以及女性的雌二醇水平。
所有10名男性在治疗期间均出现无精子症或严重少精子症;12个月后,除1人外,所有人的精子计数均正常,FSH水平也正常。在女性接受环磷酰胺治疗期间,所有患者均出现闭经。治疗停止后,A组所有女性开始规律月经,随访结束时,所有女性均显示有排卵周期。在整个观察期内,激素水平无显著变化。6名女性怀孕,妊娠成功足月,无并发症。在B组中,所有4名女性均出现持续性闭经;治疗结束和随访时的血清FSH和黄体生成素水平相对于基线显著升高;随访结束时的雌二醇水平与基线及A组相应值相比显著降低。
男性亚研究无对照,女性亚研究非随机。
该研究表明,睾酮和曲普瑞林分别对患有各种形式肾病的男性和女性环磷酰胺诱导的性腺损伤具有保护作用。