...
首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Reversibility of castration resistance status after Radium-223 dichloride treatment: clinical evidence and review of the literature
【24h】

Reversibility of castration resistance status after Radium-223 dichloride treatment: clinical evidence and review of the literature

机译:镭至223二氯化物处理后阉割性能的可逆性:文学的临床证据和审查

获取原文
获取原文并翻译 | 示例
           

摘要

In the history of prostate cancer, some of the patients progressed to castration-resistant prostate cancer (CRPC) stage and, although new drugs and treatment protocols have been introduced, CRPC presents poor prognosis. This review is focused on biological mechanisms, underlying CRPC described in scientific literature in order to explain the reversion of resistance to castration. We present the case of a 73-year-old man, affected by bone metastatic CRPC, early treated with Radium-223 with a complete response. After 15 months from Radium-223 treatment, prostate-specific antigen increased with radiological progression. Androgen deprivation therapy was again performed and was effective, despite previous CRPC condition and no known mechanisms that may explain the reversion of this condition. Therefore, to our knowledge, he is the unique described case of the reversion of resistance to castration. Nevertheless, promising aspects may be lack of intrametastatic production of androgen or the suppression of bypass androgen receptor signaling pathways. Furthermore, the cytotoxic action of Radium-223 on cancer stem cell (CSC), due to surrounding clones with high-bone turnover, or the immune response that underlying the abscopal effect, may also modulate the reversion of CRPC after Radium-223. If confirmed by multicenter trials, the reversion of CRPC may impact on the management of prostate cancer.
机译:在前列腺癌的历史中,一些患者进展到抗阉割的前列腺癌(CRPC)阶段,虽然已经引入了新的药物和治疗方案,但CRPC预后差不多。本综述专注于生物机制,科学文献中描述的基础CRPC,以解释抵抗阉割的逆转。我们展示了一个73岁的人,受到骨转移性CRPC影响的73岁男性,早期用镭223治疗,具有完全反应。从镭〜223处理15个月后,前列腺特异性抗原随着放射进展而增加。尽管先前的CRPC病症,并且没有可知的机制,但雄激素剥夺疗法再次进行并且是有效的,并且没有可解释这种情况的逆转的已知机制。因此,为了我们的知识,他是逆转阉割的独特描述的情况。然而,有希望的方面可能缺乏雄激素的脑内横向性或抑制旁路雌激素受体信号传导途径。此外,由于周围克隆具有高骨周转的克隆,或俯冲效应下面的免疫应答,因此,克里氨酰-223对癌症干细胞(CSC)的细胞毒作用也可能还可以调节镭〜223后CRPC的逆转。如果通过多中心试验证实,CRPC的逆转可能会影响前列腺癌的管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号