Department of Nuclear Medicine, University Hospital Bonn, Bonn, Germany.
J Nucl Med. 2011 Nov;52(11):1721-6. doi: 10.2967/jnumed.111.093674. Epub 2011 Oct 5.
This retrospective study compared the effects of single and multiple administrations of (186)Re-hydroxyethylidenediphosphonate ((186)Re-HEDP) on palliation and survival of prostate cancer patients presenting with more than 5 skeletal metastases.
A total of 60 patients were divided into 3 groups. Group A (n = 19) consisted of patients who had received a single injection; group B (n = 19), patients who had 2 injections; and group C (n = 22), patients who had 3 or more successive injections. The (188)Re-HEDP was prepared using non-carrier-added (188)Re obtained from an in-house (188)W/(188)Re generator after dilution with carrier perrhenate. Patients' data available from the referring physicians-including prostate-specific antigen levels-were entered into a Windows-based matrix and analyzed using a statistical program. The Gleason scores were similar for all 3 groups.
Mean survival from the start of treatment was 4.50 ± 0.81 mo (95% confidence interval [CI], 2.92-6.08) for group A, 9.98 ± 2.21 mo (95% CI, 5.65-14.31) for group B, and 15.66 ± 3.23 (95% CI, 9.33-22.0) for group C. Although the 3 groups did not differ in Gleason score, the number of lost life-years was significantly lower in group C than in groups A and B. Pain palliation was achieved in 89.5% of group A, 94.7% of group B, and 90.9% of group C.
Posttreatment overall survival could be improved from 4.50 to 15.66 mo by multiple-injection bone-targeted therapy with (188)Re-HEDP, when compared with a single injection. Significant pain palliation was common and independent of administration frequency.
本回顾性研究比较了单次和多次给予(186)Re-羟乙基二膦酸盐((186)Re-HEDP)对有 5 个以上骨转移的前列腺癌患者的缓解和生存的影响。
共 60 例患者分为 3 组。A 组(n=19)为单次注射组;B 组(n=19)为 2 次注射组;C 组(n=22)为 3 次或更多连续注射组。(188)Re-HEDP 采用非载体添加(188)Re 从内部(188)W/(188)Re 发生器中获得,然后用载体高铼酸盐稀释。从转诊医生处获得的患者数据,包括前列腺特异性抗原水平,输入到基于 Windows 的矩阵中,并使用统计程序进行分析。所有 3 组的 Gleason 评分相似。
A 组从治疗开始的平均生存时间为 4.50±0.81 个月(95%置信区间[CI],2.92-6.08),B 组为 9.98±2.21 个月(95%CI,5.65-14.31),C 组为 15.66±3.23(95%CI,9.33-22.0)。尽管 3 组的 Gleason 评分没有差异,但 C 组的生命损失年数明显低于 A 组和 B 组。A 组、B 组和 C 组的疼痛缓解率分别为 89.5%、94.7%和 90.9%。
与单次注射相比,多次(188)Re-HEDP 骨靶向治疗可将总生存时间从 4.50 个月提高到 15.66 个月。显著的疼痛缓解是常见的,与给药频率无关。