Testis and penile cancers in kidney transplant recipients: A systematic review of epidemiology, treatment options and oncological outcomes by the EAU-YAU Penile and Testis Cancer Working Group.

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Tác giả: M Bandini, G Basile, A Breda, W Cazzaniga, L Dieguez, G Fallara, C Fankhauser, F Montorsi, F Negri, A Salonia, A Territo

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Spain : Actas urologicas espanolas , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 97771

INTRODUCTION: Kidney transplant (KT) recipients are at an elevated risk of developing de novo cancers. However, penile (PeCa) and testis cancers have received limited attention in this setting. OBJECTIVE: To summarize the epidemiology, treatment options, and oncological outcomes of penile and testis cancer in KT recipients. EVIDENCE ACQUISITION: We conducted a systematic review of prospective, retrospective and national transplant registries studies published up to December 2023. Data on the incidence of penile and testis cancers among KT recipients, diagnostic protocols, screening recommendations, and therapeutic strategies tailored for KT recipients were collected. The risk of bias (RoB) of included studies was determined using the Newcastle and Ottawa scale. EVIDENCE SYNTHESIS: Overall, 21 studies involving 67924 KT male recipients were included. PeCa was diagnosed in 33 patients, yielding an incidence ranging from 0.04% to 0.3%. Additionally, 67 cases of testicular cancer were recorded, with an incidence ranging from 0.03% to 0.55%. Most tumors were localized, and histology variants were uncommon. While the surgical treatment of the primary tumor remains consistent with that of the general population, the use of radiotherapy and cytotoxic treatments are less frequently reported in this setting. These therapies should be considered on an individualized basis to minimize the risk of graft injury. CONCLUSIONS: Penile and testis cancers are relatively uncommon among KT recipients. General screening protocols and deviation from current treatment guidelines are not recommended in localized diseases. Given the risk of graft damage, any non-cytotoxic option should be preferred in locally advanced cases.
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