摘要
前列腺癌(PCa)是西方国家男性最常见的肿瘤,也是最相关的死亡原因之一。雄激素剥夺疗法(ADT)是一种广泛应用于晚期前列腺癌的治疗方法。当前列腺癌进展,尽管ADT和阉割水平睾酮,严重的临床条件称为转移性阉割抵抗前列腺癌(mCRPC)发生。治疗mCRPC的唯一方法是以紫杉烷类化疗为代表多年。然而,最近引入的治疗方法,如第二代抗雄激素(如enzalutamide和abiraterone)、sipuleucel-T细胞免疫治疗或223ra -二氯靶向α治疗,显著改变了mCRPC的预后。这些新颖的治疗方法需要一种尚未满足的成像生物标志物,用于患者治疗前的分层和反应评估。在这种情况下,核医学可以提供多种代谢和分子探针来研究细胞和亚细胞水平的病理过程。本文的目的是回顾到目前为止发表的有关这一主题的文献中最相关的发现,特别强调每种示踪剂的优点和缺点,并涵盖定义个性化治疗方法的未来前景。
关键词: 前列腺癌,去势抵抗,抗雄激素,雄激素受体,18f -胆碱,骨扫描,18氟氯胺,前列腺特异性膜抗原。
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