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男性性腺毒性。

Male gonadal toxicity.

作者信息

Meistrich Marvin L

机构信息

Department of Experimental Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.

出版信息

Pediatr Blood Cancer. 2009 Aug;53(2):261-6. doi: 10.1002/pbc.22004.

Abstract

Cancer treatment with chemotherapy or radiotherapy causes gonadal toxicity in male patients. The endpoint of most concern for future reproductive options is the induction of prolonged azoospermia, which may or may not be reversible. The immediate effects of therapy and its reversibility are most readily observed in post-pubertal patients, but the same antineoplastic regimens given to prepubertal males can induce permanent azoospermia. The probability of permanent azoospermia is related to the specific agents used and their doses. The most damaging are alkylating agents (particularly chlorambucil, procarbazine, cyclophosphamide, melphalan, and busulfan), cisplatin and radiation to the region of the testicles.

摘要

化疗或放疗用于癌症治疗会导致男性患者出现性腺毒性。对于未来生殖选择而言,最令人担忧的终点是诱发长期无精子症,这种情况可能可逆,也可能不可逆。治疗的即时效应及其可逆性在青春期后患者中最容易观察到,但给予青春期前男性相同的抗肿瘤方案可诱发永久性无精子症。永久性无精子症的概率与所使用的特定药物及其剂量有关。最具损害性的是烷化剂(尤其是苯丁酸氮芥、丙卡巴肼、环磷酰胺、美法仑和白消安)、顺铂以及睾丸区域的放疗。

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