Department of Urology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan.
Int J Clin Oncol. 2013 Jun;18(3):472-7. doi: 10.1007/s10147-012-0406-8. Epub 2012 Apr 11.
To ascertain the anti-tumor effect of zoledronic acid (ZOL) treatment on clinical outcomes in patients with bone metastatic prostate cancer, we examined the effect of ZOL started simultaneously with hormonal therapy as initial treatment in these patients.
Forty-seven patients with bone-metastatic prostate cancer who received a luteinizing hormone releasing-hormone (LHRH) analogue and an anti-androgen [maximal androgen blockade (MAB)] were assigned to receive ZOL (4 mg intravenous administration every month for 2 years). The time to progression (TTP) of the prostate-specific antigen (PSA), the overall survival (OS), and the rate of PSA decrease in patients with MAB and ZOL treatment (ZOL group) were compared with these parameters in patients who received only MAB at one institute as a control group (non-ZOL group).
Although the nadir PSA level and the rate of PSA normalization showed no significant differences between the ZOL and non-ZOL groups, the time to nadir PSA in the ZOL group was significantly shorter than that in the non-ZOL group (P < 0.05, Mann-Whitney U-test). There was a significant difference in TTP (P = 0.017, log-rank test) between the ZOL and non-ZOL groups, and statistically significant differences in TTP and OS between the ZOL and non-ZOL groups (P = 0.044 and 0.035, log-rank test) were recognized particularly in patients with advanced disease (extension of disease, grade 3 and 4).
Simultaneous administration of ZOL and MAB as initial treatment delayed TTP in bone-metastatic prostate cancer patients. Initial treatment with ZOL has the possibility of anti-tumor activity to delay disease progression.
为了确定唑来膦酸(zoledronic acid,ZOL)治疗对骨转移前列腺癌患者临床结局的抗肿瘤作用,我们研究了 ZOL 与激素治疗同时作为初始治疗在这些患者中的效果。
47 例接受促黄体激素释放激素(luteinizing hormone releasing-hormone,LHRH)类似物和抗雄激素[最大雄激素阻断(maximal androgen blockade,MAB)]治疗的骨转移前列腺癌患者被分配接受 ZOL(4 mg 静脉注射,每月一次,持续 2 年)。我们比较了 MAB 和 ZOL 治疗(ZOL 组)患者的前列腺特异性抗原(prostate-specific antigen,PSA)进展时间(time to progression,TTP)、总生存期(overall survival,OS)和 PSA 下降率与在同一机构仅接受 MAB 作为对照的患者(非 ZOL 组)的这些参数。
尽管 ZOL 组和非 ZOL 组的 PSA 最低值和 PSA 正常化率无显著差异,但 ZOL 组的 PSA 最低值时间明显短于非 ZOL 组(P < 0.05,Mann-Whitney U 检验)。ZOL 组和非 ZOL 组的 TTP 存在显著差异(P = 0.017,对数秩检验),ZOL 组和非 ZOL 组的 TTP 和 OS 也存在统计学差异(P = 0.044 和 0.035,对数秩检验),尤其是在疾病进展(疾病扩展、3 级和 4 级)的患者中。
ZOL 和 MAB 同时作为初始治疗延迟了骨转移前列腺癌患者的 TTP。ZOL 作为初始治疗可能具有抗肿瘤活性,可延缓疾病进展。