Publication | Closed Access
Fertility after chemotherapy for testicular germ cell cancers.
296
Citations
11
References
1997
Year
The study aims to determine the likelihood of spermatogenesis recovery after orchidectomy and cisplatin‑based chemotherapy for testicular germ cell cancer. A retrospective cohort of 178 patients (170 with follow‑up) was analyzed, with sperm counts measured pre‑ and post‑chemotherapy, classified as normospermic, oligospermic, or azoospermic, and followed for a median of 30 months. Among 170 patients reassessed ≥1 year post‑chemotherapy, 64 % remained normospermic, 16 % became oligospermic, and 20 % azoospermic; spermatogenesis recovery rose to 48 % at 2 years and 80 % at 5 years, with higher recovery after carboplatin and lower after >4 cycles, and a prognostic model stratifying patients into 25 %, 45 %, and 82 % recovery probabilities by 2 years.
PURPOSE To analyze the probability of recovery of spermatogenesis after orchidectomy and cisplatin-based chemotherapy (CT) for testicular germ cell cancer. PATIENTS AND METHODS One hundred seventy-eight patients treated between 1979 and 1991 were selected by the requirement of sperm count both pre-CT and post-CT. Counts were classified as normospermic (NS) if more than 10 x 10(6)/mL, oligospermic (OS) if 1 to 9 x 10(6)/mL, and azoospermic (AS) if less than 1 x 10(6)/mL. The median follow-up time after CT before sperm analysis was 30 months. RESULTS Analysis of 170 patients whose spermatogenesis was reassessed at least 1 year after CT showed that of 89 patients whose pre-CT counts were NS, the post-CT count was NS in 64%, OS in 16%, and AS in 20%. There was clear evidence for continued recovery beyond 1 year; the probability of spermatogenesis increased to 48% by 2 years and 80% by 5 years. There was a significantly higher probability of recovery to OS and NS count levels in the 54 patients treated with carboplatin-rather than cisplatin-based therapy. There was an independent and similar effect of normal pre-CT count. There was a reduced probability to recover to OS in the 26 patients treated with more than four cycles of CT. A prognostic model identified three groups with 25%, 45%, and 82% probabilities of recovering spermatogenesis by 2 years after CT. CONCLUSION Analysis of pre-CT sperm count together with details of planned treatment can be used to predict recovery of spermatogenesis following germ cell CT.
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