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Radium-223 and metastatic castration-resistant prostate cancer: All that glitters is not gold

机译:镭223和转移性去势抵抗性前列腺癌:闪闪发光的不是黄金

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摘要

After being approved by the National Drug Agency in several countries, Radium-223 (Ra-223) is gaining wide acceptance in the treatment of bone metastatic castration resistant prostate cancer. The exact mechanism of action remain unclear: The established model of direct alpha-particle irradiation from the remodelling bone surface, where Ra-223 accumulates, surrounding the tumor foci can explain a lethal effect only on metastatic microdeposits, but not on higher tumor burden. According to the “pre-metastatic niche model”, it is likely that Ra-223 targets several non-tumoral cell types of the tumor microenvironment involved in the complex mechanism of cancer bone homing and colonization. A deeper insight into this hypothetical mechanism will lead to a more accurate dosimetric approach and to find optimal sequencing and/or combination with the other therapeutic options.
机译:在数个国家获得美国国家药物管理局(National Drug Agency)批准后,镭223(Ra-223)在治疗骨转移性去势抵抗性前列腺癌中获得了广泛的接受。确切的作用机理尚不清楚:围绕重塑肿瘤表面的重塑骨表面直接α-粒子辐射的建立模型(Ra-223积累在该模型周围)仅能解释对转移性微沉积的致死作用,而对较高的肿瘤负担无解释作用。根据“转移前的利基模型”,Ra-223可能靶向与肿瘤骨归巢和定植复杂机制有关的肿瘤微环境的几种非肿瘤细胞类型。对这种假设机制的更深入的了解将导致更准确的剂量学方法,并找到最佳的测序和/或与其他治疗选择的组合。

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