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Concurrent use of Sr-89 chloride with zoledronic acid is safe and effective for breast cancer patients with painful bone metastases

机译:Sr-89氯化物与唑来膦酸同时使用对患有骨转移疼痛的乳腺癌患者是安全有效的

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摘要

Our aim in this study was to examine the safety and efficacy of the concurrent use of the radiopharmaceutical strontium-89 (Sr-89) chloride with zoledronic acid in standard anticancer therapy for breast cancer patients with painful multifocal bone metastases. The study comprised 16 breast cancer patients with painful multifocal bone metastases detected by bone scintigraphy, computed tomography or magnetic resonance imaging. All patients were treated with Sr-89 and zoledronic acid concurrently between March 2007 and February 2011 as part of a standard therapeutic regimen comprising chemotherapy, endocrine therapy, molecular targeting therapy and targeted radiotherapy. Sr-89 was administered intravenously at 2 MBq/kg to a maximum of 141 MBq per person. Safety was evaluated according to myelotoxicity as measured by the Common Terminology Criteria for Adverse Events (v3.0). To assess treatment efficacy, we monitored changes in analgesic drug dosages. Furthermore, bremsstrahlung imaging after the administration of Sr-89 was utilized to examine the relationship between the accumulation of Sr-89 in metastatic sites and treatment efficacy. Based on the results, a total of 14 out of 16 patients (88%) reported bone pain relief, indicating a high efficacy of Sr-89 combined with zoledronic acid. In responsive cases, a strong uptake of Sr-89 was observed on bremsstrahlung imaging at the same sites indicated by 99mTc bone scintigraphy. Moreover, severe myelosuppression (> grade 3) was not observed, and adverse events were tolerable. In conclusion, the use of Sr-89 with zoledronic acid in breast cancer patients with painful bone metastases was safe and effective when administered concurrently with other standard therapies. In the future, the treatment with Sr-89 at the early stage should be considered, and a large-scale clinical study should be conducted.
机译:我们在这项研究中的目的是检验在放射性痛伴多灶性骨转移的乳腺癌患者中,同时使用放射性药物锶89(Sr-89)和唑来膦酸的安全性和有效性。该研究包括16例乳腺癌患者,这些患者通过骨闪烁显像,计算机断层扫描或磁共振成像检测出多灶性骨转移疼痛。在2007年3月至2011年2月之间,所有患者均同时接受Sr-89和唑来膦酸治疗,这是包括化疗,内分泌治疗,分子靶向治疗和靶向放疗在内的标准治疗方案的一部分。 Sr-89的静脉注射剂量为2 MBq / kg,每人最大剂量为141 MBq。根据由不良事件通用术语标准(v3.0)测得的骨髓毒性评估安全性。为了评估治疗效果,我们监测了止痛药剂量的变化。此外,施用Sr-89后的致辐射成像被用于检查Sr-89在转移部位的蓄积与治疗效果之间的关系。根据结果​​,总共16名患者中有14名(88%)报告了骨痛缓解,表明Sr-89与唑来膦酸联用具有很高的疗效。在有反应的情况下,在 99m Tc骨闪烁显像术显示的相同部位,在致辐射成像中观察到Sr-89的强烈摄取。此外,未观察到严重的骨髓抑制(> 3级),并且不良事件是可以忍受的。总之,与其他标准疗法同时使用时,将Sr-89与唑来膦酸一起用于患有骨痛转移的乳腺癌患者是安全有效的。将来,应考虑早期使用Sr-89进行治疗,并应进行大规模的临床研究。

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