Bahadur G, Ozturk O, Muneer A, Wafa R, Ashraf A, Jaman N, Patel S, Oyede A W, Ralph D J
Fertility and Reproductive Medicine Laboratories, Department of Obstetrics and Gynaecology, Royal Free and University College Medical School, University College Hospitals Trust, Rosenheim Building, 25 Grafton Way, London WC1E 6DB, UK.
Hum Reprod. 2005 Mar;20(3):774-81. doi: 10.1093/humrep/deh671. Epub 2005 Feb 2.
The aim of this study was to analyse the semen quality of patients before and after gonadotoxic therapy.
We evaluated semen quality in 314 patients over a 26 year period. The diagnostic categories were leukaemia (n = 13); lymphoma (n = 128); testicular cancer (n = 102); benign conditions (n = 13); and other malignant neoplasms (n = 58). The degree of azoospermia or oligozoospermia for each disease category was recorded. We then analysed the recovery in semen quality over time for each disease category.
The mean patient age was 27.9 years (range 13-65 years). A total of 1115 post-treatment semen samples were analysed from 314 patients. There was a significant reduction in the post-treatment sperm concentration, sperm motility and semen volume compared with pre-treatment levels (P < 0.05) in the entire cohort. However, the sperm movement and motility grade remained unaffected. Patients with testicular carcinoma had the lowest pre-treatment sperm concentrations but also the lowest incidence of azoospermia after cancer treatment. Patients with lymphoma and leukaemia had the highest incidence of post-treatment azoospermia and oligospermia. Patients having the largest reductions in their sperm concentration after treatment required the longest recovery period for spermatogenesis. The diagnostic category was the only significant predictor of post-treatment azoospermia.
Gonadotoxic treatment results in a significant reduction in sperm quality. The type of cancer or disease, and the pre-treatment sperm concentrations were found to be the most significant factors governing post-treatment semen quality and recovery of spermatogenesis. All categories of patients displayed varying degrees of azoospermia and oligozoospermia, and recovery of gonadal function from these states was not significant. This highlights the importance of ensuring sperm banking before treatment, including for patients with benign conditions. Several factors and associations are discussed further in order to give an insight into the pre- and post-gonadotoxic treatment effects.
本研究旨在分析性腺毒性治疗前后患者的精液质量。
我们在26年期间评估了314例患者的精液质量。诊断类别包括白血病(n = 13);淋巴瘤(n = 128);睾丸癌(n = 102);良性疾病(n = 13);以及其他恶性肿瘤(n = 58)。记录了每个疾病类别的无精子症或少精子症程度。然后我们分析了每个疾病类别随时间的精液质量恢复情况。
患者的平均年龄为27.9岁(范围13 - 65岁)。共分析了来自314例患者的1115份治疗后精液样本。与治疗前水平相比,整个队列中治疗后精子浓度、精子活力和精液量均显著降低(P < 0.05)。然而,精子运动和活力等级未受影响。睾丸癌患者治疗前精子浓度最低,但癌症治疗后无精子症发生率也最低。淋巴瘤和白血病患者治疗后无精子症和少精子症的发生率最高。治疗后精子浓度降低幅度最大的患者精子发生恢复所需时间最长。诊断类别是治疗后无精子症的唯一显著预测因素。
性腺毒性治疗导致精子质量显著降低。发现癌症或疾病类型以及治疗前精子浓度是决定治疗后精液质量和精子发生恢复的最重要因素。所有类别患者均表现出不同程度的无精子症和少精子症,且性腺功能从这些状态恢复不显著。这凸显了在治疗前确保精子冻存的重要性,包括患有良性疾病的患者。进一步讨论了几个因素及关联,以便深入了解性腺毒性治疗前后的影响。