Bruland Øyvind S, Nilsson Sten, Fisher Darrell R, Larsen Roy H
Faculty of Medicine, University of Oslo and Department of Oncology, The Norwegian Radium Hospital, Norway.
Clin Cancer Res. 2006 Oct 15;12(20 Pt 2):6250s-6257s. doi: 10.1158/1078-0432.CCR-06-0841.
The bone-seeking, alpha-particle-emitting radiopharmaceutical Alpharadin, 223RaCl2 (half-life=11.4 days), is under clinical development as a novel treatment for skeletal metastases from breast and prostate cancer. This article summarizes the current status of preclinical and clinical research on 223RaCl2. Potential advantages of 223Ra to that of external beam irradiation and registered beta-emitting bone seekers are discussed. Published data of 223Ra dosimetry in mice and a therapeutic study in a skeletal metastases model in nude rats have indicated significant therapeutic potential of bone-seeking alpha-emitters. This article provides short-term and long-term results from the first clinical single dosage trial. We also present data from a repeated dosage study of five consecutive injections of 50 kBq/kg body weight, once every 3rd week, or two injections of 125 kBq/kg body weight, 6 weeks apart. Furthermore, interim results are described for a randomized phase 2 trial involving 64 patients with hormone-refractory prostate cancer and painful skeletal metastases who received four monthly injections of 223Ra or saline as an adjuvant to external beam radiotherapy. Lastly, we present preliminary dose estimates for 223Ra in humans. Results indicate that repeated dosing is feasible and toxicity is low, and that opportunities are available for combined treatment strategies.
亲骨性、发射α粒子的放射性药物氯化镭-223(Alpharadin,半衰期 = 11.4天)正处于临床开发阶段,作为一种治疗乳腺癌和前列腺癌骨转移的新型疗法。本文总结了氯化镭-223的临床前和临床研究现状。讨论了镭-223相对于外照射和已获批的发射β粒子的亲骨性药物的潜在优势。已发表的关于小鼠体内镭-223剂量测定的数据以及一项在裸鼠骨转移模型中的治疗研究表明,亲骨性发射α粒子的药物具有显著的治疗潜力。本文提供了首个临床单剂量试验的短期和长期结果。我们还展示了一项重复剂量研究的数据,该研究为连续5次注射,剂量为50 kBq/kg体重,每3周注射一次,或两次注射,剂量为125 kBq/kg体重,间隔6周。此外,还描述了一项随机2期试验的中期结果,该试验涉及64例激素难治性前列腺癌伴疼痛性骨转移患者,他们接受每月4次注射氯化镭-223或生理盐水,作为外照射放疗的辅助治疗。最后,我们给出了人体中镭-223的初步剂量估计。结果表明重复给药是可行的且毒性较低,并且存在联合治疗策略的机会。