Research Papers:
Increased risk of testis failure in testicular germ cell tumor survivors undergoing radiotherapy
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Abstract
Marco Ghezzi1,*, Luca De Toni1,*, Pierfrancesco Palego1, Massimo Menegazzo1, Elisa Faggian1, Massimiliano Berretta2, Francesco Fiorica3, Maurizio De Rocco Ponce1, Carlo Foresta1 and Andrea Garolla1
1Unit of Andrology and Reproductive Medicine, Department of Medicine, University of Padova, Padova, Italy
2Department of Medical Oncology, National Cancer Institute, IRCCS Aviano, Aviano, Italy
3Department of Radiotherapy, University Hospital Sant'Anna, Ferrara, Italy
*These authors contributed equally to this work
Correspondence to:
Andrea Garolla, email: [email protected]
Keywords: sperm parameters; luteinizing hormone; vitamin D; parathormone; Leydig cells
Received: June 26, 2017 Accepted: November 15, 2017 Published: December 07, 2017
ABSTRACT
Testicular germ cell tumors (TGCTs) are prevalent in males of reproductive age. Among the available therapeutic choices, pelvic radiotherapy (RT) and simple surveillance (SURV) are usually pursued. However, RT is considered to have life-threatening effects on testicular functions. In this study we sought to clarify this issue by evaluating sperm parameters and sex hormones in 131 TGCTs RT-treated-patients at both baseline (T0) and 12 (T1) and 24 months (T2) of follow-up. An age-matched group of 61 SURV patients served as control. Sperm parameters were comparable between SURV and RT at T0.
The RT group showed a significant reduction of all sperm parameters at T1 (all P values < 0.05 vs T0 and vs SURV at T1) and increased levels of sperm aneuploidies, with some degree of recovery at T2. On the other hand, despite normal levels of total testosterone being detected in both groups, luteinizing hormone (LH) levels in the RT group progressively increased at T1 and T2 with a relative risk of developing subclinical hypogonadism of 3.03 (95% CI: 1,50–6,11) compared to SURV. Again, compared to SURV, exposure to RT was associated with a 5.78 fold (95% CI: 2,91–11,48) risk of developing vitamin D insufficiency. These data suggest a likely RT-dependent impairment of the Leydig cell compartment.
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