Nightengale B, Brune M, Blizzard S P, Ashley-Johnson M, Slan S
College of Pharmacy, University of Oklahoma, Oklahoma City 73190, USA.
Am J Health Syst Pharm. 1995 Oct 15;52(20):2189-95. doi: 10.1093/ajhp/52.20.2189.
The role of strontium chloride Sr 89 in the palliative treatment of pain associated with metastatic bone disease is reviewed. Conventional therapies to relieve metastatic bone pain include nonopioid and opioid analgesics, hormonal therapy, external-beam irradiation, and chemotherapy. Limitations in the long-term safety and effectiveness of these treatments have increased interest in using systemic radioactive isotopes for palliation of pain. Strontium chloride Sr 89 is a relatively new bone-seeking radiopharmaceutical that has FDA-approved labeling for use in relieving pain associated with skeletal metastases. An analogue of calcium, strontium chloride Sr 89 is rapidly cleared from the blood after i.v. injection. The agent selectively irradiates metastatic sites while generally sparing normal soft-bone tissue. In clinical studies, a majority of patients with prostate or breast cancer obtained substantial relief from bone pain after receiving strontium chloride Sr 89 alone or in combination with external-beam irradiation. Adverse effects tend to be mild, but patients should be monitored for possible hematologic toxicity. Patients should discontinue any calcium-containing products before receiving the agent. The typical dose is 4 mCi (148 MBq) administered by slow i.v. push over one to two minutes; doses can be repeated at three-month intervals. Pain relief usually begins in 10-20 days and lasts up to six months. Radiation safety measures are necessary in handling strontium chloride Sr 89 and the wastes of patients. Strontium chloride Sr 89 is costly, but preliminary analysis indicates that it may reduce management expenditures overall.(ABSTRACT TRUNCATED AT 250 WORDS)
本文综述了氯化锶 Sr 89 在转移性骨病相关疼痛姑息治疗中的作用。缓解转移性骨痛的传统疗法包括非阿片类和阿片类镇痛药、激素疗法、外照射放疗和化疗。这些治疗方法在长期安全性和有效性方面的局限性,增加了人们对使用全身放射性同位素缓解疼痛的兴趣。氯化锶 Sr 89 是一种相对较新的亲骨性放射性药物,已获得美国食品药品监督管理局(FDA)批准用于缓解与骨转移相关的疼痛。作为钙的类似物,静脉注射后,氯化锶 Sr 89 能迅速从血液中清除。该药物能选择性地照射转移部位,同时通常可使正常的软骨组织免受辐射。在临床研究中,大多数前列腺癌或乳腺癌患者在单独接受氯化锶 Sr 89 或与外照射放疗联合使用后,骨痛得到了显著缓解。不良反应往往较轻,但应监测患者是否可能出现血液学毒性。患者在接受该药物之前应停用任何含钙产品。典型剂量为 4 毫居里(148 兆贝可),通过静脉缓慢推注,在 1 至 2 分钟内给药;剂量可每三个月重复一次。疼痛缓解通常在 10 - 20 天开始,持续长达六个月。处理氯化锶 Sr 89 及其患者的排泄物时,必须采取辐射安全措施。氯化锶 Sr 89 成本高昂,但初步分析表明,它可能总体上降低管理费用。(摘要截选至 250 字)