Department of Medical Oncology, Cancer Hospital and Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 17 Panjiayuan Nanli, Chaoyang District, Beijing 100021, China.
Breast. 2012 Aug;21(4):544-9. doi: 10.1016/j.breast.2012.04.008. Epub 2012 May 22.
To evaluate the long-term tolerability and activity of prolonged administration of bisphosphonates (BPs) in breast cancer (BrCa) patients with bone metastasis (BM).
We retrospectively analyzed safety data and activity of BPs in BrCa patients with BM who had received intravenous BPs for >24 months. Renal toxicity, osteonecrosis of the jaw (ONJ), and hypocalcemia were assessed. In addition, levels of creatinine (Cr) and calcium (Ca) in pre- and post-treatment sera were examined. The following parameters were also analyzed: the proportion of patients with at least one skeletal-related event (SRE), the distribution of each type of SRE, and the skeletal morbidity rate (SMR).
181 patients from January 1, 2005 to May 31, 2009 were enrolled in the study. The median BP administration period was 36 (range: 25-133) months. Grades 1-2 and 3 renal toxicity occurred in 3.9% and 0.7% of patients, respectively. Only one patient was diagnosed with ONJ, the incidence rate of which was 0.6%. Hypocalcemia occurred in 29 patients (16.0%), most frequently after two years of BP therapy. Neither serum Cr levels nor the creatinine clearance rate were significantly increased by treatment. Furthermore, 50 patients (27.6%) experienced a new SRE between zero and 24 months after BP therapy. However, no notable increase in incidence rate of SREs was observed after the two years of BP treatment. Overall, 63 patients (34.8%) experienced at least one new SRE after initiation of BPs (p = 0.173). No significant difference was found among the different BP subgroups of pamidronate, ibandronate, and zoledronate. Radiation to bone was the most common cause of SREs (68.4%, 67/98). SMR was 0.10 events per year for 0-5 years after BP treatment.
This was the largest retrospective study of extended use of BPs in BrCa patients with BM. Intravenous administration of BPs was well-tolerated and remained active throughout the prolonged period of administration. The occurrence of SREs was similar among the pamidronate, ibandronate, and zoledronate subgroups after two years of BP treatment.
评估乳腺癌(BrCa)伴骨转移(BM)患者延长双膦酸盐(BPs)给药的长期耐受性和疗效。
我们回顾性分析了接受静脉 BPs 治疗超过 24 个月的 BrCa 伴 BM 患者的安全性数据和 BPs 的疗效。评估了肾毒性、颌骨坏死(ONJ)和低钙血症。此外,还检测了治疗前后血清中肌酐(Cr)和钙(Ca)的水平。还分析了以下参数:至少发生一次骨骼相关事件(SRE)的患者比例、每种 SRE 的分布以及骨骼发病率(SMR)。
2005 年 1 月 1 日至 2009 年 5 月 31 日期间,共纳入 181 例患者。BP 治疗中位时间为 36(范围:25-133)个月。分别有 3.9%和 0.7%的患者出现 1-2 级和 3 级肾毒性。仅 1 例患者诊断为 ONJ,发生率为 0.6%。29 例(16.0%)患者发生低钙血症,多发生在 BP 治疗 2 年后。治疗后血清 Cr 水平或肌酐清除率均无明显升高。此外,50 例(27.6%)患者在 BP 治疗后 0-24 个月内出现新的 SRE。但在 BP 治疗 2 年后,SRE 的发生率未见明显增加。总体而言,63 例(34.8%)患者在开始使用 BPs 后至少发生了一次新的 SRE(p=0.173)。不同 BP 亚组(帕米膦酸盐、伊班膦酸盐和唑来膦酸盐)之间无显著差异。放射性骨治疗是 SRE 最常见的原因(68.4%,67/98)。BP 治疗后 0-5 年 SMR 为每年 0.10 次事件。
这是最大的关于乳腺癌伴骨转移患者延长使用 BPs 的回顾性研究。静脉内给予 BPs 耐受性良好,在延长治疗期间保持有效。BP 治疗 2 年后,帕米膦酸盐、伊班膦酸盐和唑来膦酸盐亚组的 SRE 发生率相似。