Pharmatest Services Ltd, Turku, Finland.
J Natl Cancer Inst. 2013 Jun 19;105(12):908-16. doi: 10.1093/jnci/djt116. Epub 2013 May 16.
Bone metastases are associated with increased morbidity and poor prognosis in breast cancer patients. Radium-223 dichloride is a calcium mimetic that localizes to bone, providing targeted therapy for skeletal metastasis.
We investigated the mode of action of radium-223 dichloride using breast cancer cell, osteoclast, and osteoblast cultures as well as a mouse model of breast cancer bone metastasis. A single dose of radium-223 dichloride was used in three different settings mimicking the prevention or treatment of bone metastasis. Disease progression was monitored using fluorescence and radiographic imaging and histological analyses. The effect of radium-223 dichloride alone and in combination with doxorubicin or zoledronic acid on survival of mice was analyzed by Kaplan-Meier methods. All statistical tests used were two-sided.
Radium-223 dichloride incorporated into bone matrix and inhibited proliferation of breast cancer cells and differentiation of osteoblasts and osteoclasts (all P values < .001) in vitro. In an established bone metastasis setting, radium-223 dichloride prevented tumor-induced cachexia (0/14 vs 7/14 control mice) and decreased osteolysis by 56% and tumor growth by 43% (all P values < .05). Radium-223 dichloride induced double-strand DNA breaks in cancer cells in vivo. Finally, radium-223 dichloride extended survival as a monotherapy (29.2 days, 95% confidence interval [CI] = 26.6 to 31.8 days, P = .039) and in combination with zoledronic acid (31.4 days, 95% CI = 28.8 to 34.0 days, P = .004) or doxorubicin (31.5 days, 95% CI = 29.5 to 33.5 days, P < .001) compared to the vehicle group (24.9 days, 95% CI = 23.4 to 26.4 days). Similar but even more pronounced effects were observed when radium-223 dichloride was administered in a preventive or micrometastatic setting.
Our findings strongly support the development of radium-223 dichloride for the treatment of breast cancer patients with or at high risk of developing bone metastases.
骨转移与乳腺癌患者发病率增加和预后不良有关。镭-223 二氯化物是一种钙类似物,可定位于骨骼,为骨骼转移提供靶向治疗。
我们使用乳腺癌细胞、破骨细胞和成骨细胞培养物以及乳腺癌骨转移小鼠模型研究了镭-223 二氯化物的作用机制。在三种不同的情况下使用单次镭-223 二氯化物剂量,模拟预防或治疗骨转移。使用荧光和放射影像学以及组织学分析监测疾病进展。通过 Kaplan-Meier 方法分析单独使用镭-223 二氯化物以及与多柔比星或唑来膦酸联合使用对小鼠生存的影响。所有使用的统计检验均为双侧检验。
镭-223 二氯化物在体外掺入骨基质中,并抑制乳腺癌细胞的增殖以及成骨细胞和破骨细胞的分化(所有 P 值均<.001)。在已建立的骨转移模型中,镭-223 二氯化物预防了肿瘤引起的恶病质(0/14 只 vs 7/14 只对照组),并使骨溶解减少 56%,肿瘤生长减少 43%(均 P 值<.05)。镭-223 二氯化物在体内诱导癌细胞的双链 DNA 断裂。最后,镭-223 二氯化物作为单一疗法(29.2 天,95%置信区间 [CI] = 26.6 至 31.8 天,P =.039)以及与唑来膦酸(31.4 天,95%CI = 28.8 至 34.0 天,P =.004)或多柔比星(31.5 天,95%CI = 29.5 至 33.5 天,P<.001)联合治疗时延长了生存时间,与载体组(24.9 天,95%CI = 23.4 至 26.4 天)相比。当在预防或微转移模型中给予镭-223 二氯化物时,观察到类似但更明显的效果。
我们的研究结果强烈支持开发镭-223 二氯化物用于治疗患有或有发生骨转移风险的乳腺癌患者。