Department of Medical Oncology, VU University Medical Centre, Amsterdam, The Netherlands.
Department of Radiology and Nuclear Medicine, VU University Medical Centre, Amsterdam, The Netherlands.
Eur Urol. 2016 Sep;70(3):416-26. doi: 10.1016/j.eururo.2015.09.005. Epub 2015 Sep 19.
The majority of patients with castration-resistant prostate cancer develop bone metastatic disease. It is often challenging to optimally palliate malignant bone pain. In case of multifocal pain due to diffuse osteoblastic metastases, treatment with bone-seeking radiopharmaceuticals can be considered.
This systematic review evaluates the efficacy of different bone-seeking radiopharmaceuticals for palliation of malignant bone pain from prostate cancer.
The PubMed (Medline) and Embase databases were searched for publications on 89-strontium-chloride ((89)Sr), 153-samarium-EDTMP ((153)Sm), 186-rhenium-HEDP ((186)Re), 188-rhenium-HEDP ((188)Re), and 223-radium-chloride ((223)Ra). Randomised controlled trials and prospective cohort studies were included. Metastatic bone pain had to be registered as outcome measure for prostate cancer patients separately.
This review included 36 articles of which 13 randomised trials and 23 prospective studies. Of all trials, 10 studies used (89)Sr, 7 (153)Sm, 12 (186)Re, 2 (188)Re, and 2 (223)Ra; three reported on a combination of different radionuclides. Only a few trials contained a blinding procedure and several studies contained incomplete follow-up or lack of intention-to-treat analysis. It was not possible to calculate a pooled estimate of pain response to treatment with any of the radionuclides because different definitions of pain response were used.
Overall, pain response percentages greater than 50-60% were seen with each radionuclide. Haematological toxicity was reported in 26 of the 36 studies and more than half of these trials stated no grade 3/4 leukopenia or thrombocytopenia occurred.
In this report we reviewed the efficacy of bone-seeking radionuclides for treating bone pain from metastatic prostate cancer. Overall, treatment with bone-seeking radionuclides resulted in pain responses greater than 50-60%.
大多数去势抵抗性前列腺癌患者会发展为骨转移疾病。优化恶性骨痛的缓解通常具有挑战性。对于弥漫性成骨转移引起的多灶性疼痛,可考虑使用亲骨性放射性药物治疗。
本系统评价评估了不同亲骨性放射性药物治疗前列腺癌骨转移所致恶性骨痛的疗效。
在 PubMed(Medline)和 Embase 数据库中搜索了关于锶-89(89Sr)、钐-153-乙二胺四甲撑膦酸(153Sm-EDTMP)、铼-186-羟乙二膦酸盐(186Re-HEDP)、铼-188-羟乙二膦酸盐(188Re-HEDP)和镭-223 氯化物(223Ra)的出版物。纳入了随机对照试验和前瞻性队列研究。转移性骨痛必须作为前列腺癌患者的单独结局指标进行登记。
本综述纳入了 36 篇文章,其中 13 项为随机试验,23 项为前瞻性研究。所有试验中,10 项研究使用了 89Sr,7 项研究使用了 153Sm,12 项研究使用了 186Re,2 项研究使用了 188Re,2 项研究使用了 223Ra;3 项研究报告了不同放射性核素的联合使用。只有少数试验采用了盲法程序,而且有几项研究的随访不完整或缺乏意向治疗分析。由于使用了不同的疼痛反应定义,因此无法计算任何放射性核素治疗疼痛反应的汇总估计值。
总体而言,每种放射性核素的疼痛反应百分比大于 50-60%。36 项研究中有 26 项报告了血液学毒性,其中一半以上的试验报告未发生 3/4 级白细胞减少或血小板减少。
在本报告中,我们回顾了亲骨性放射性核素治疗转移性前列腺癌骨痛的疗效。总体而言,亲骨性放射性核素治疗导致的疼痛反应大于 50-60%。