Kanis J A, Powles T, Paterson A H, McCloskey E V, Ashley S
WHO Collaborating Centre for Metabolic Bone Diseases, Department of Human Metabolism & Clinical Biochemistry, University of Sheffield Medical School, UK.
Bone. 1996 Dec;19(6):663-7. doi: 10.1016/s8756-3282(96)00285-2.
The aims of this study were to determine the effects of the bisphosphonate, clodronate, on the incidence of skeletal metastases and associated morbidity in women with advanced breast cancer. 133 women with recurrent breast cancer, but no evidence of skeletal metastases, were randomly allocated to receive clodronate 1600 mg daily by mouth or an identical placebo for 3 years under double-blind conditions at two clinical oncology centers in the UK and Canada. Main outcome measures included the occurrence of skeletal metastases, as judged by sequential bone scans and radiographs, and the morbidity associated with skeletal metastases comprising the incidence of hypercalcemia, vertebral, and nonvertebral fractures, and bone pain assessed by the requirements for skeletal radiotherapy. The number of patients developing skeletal metastases was lower in clodronate-treated patients than with placebo (15 vs. 19), but was not significantly different. The number of skeletal metastases was significantly lower with clodronate treatment than with placebo (32 vs. 63; p < 0.005). The complications of skeletal disease were fewer by 26% in clodronate-treated patients compared to controls (p < 0.01). Compared to placebo, significant effects in favor of clodronate were observed for vertebral deformities (29%) and nonvertebral fractures (75%), but the event frequency of each was low. There was a small (22%) but nonsignificant treatment effect on the requirements for radiotherapy and hypercalcemia (39%). There was no effect of clodronate on survival. We conclude that clodronate by mouth significantly decreases the number and complications of skeletal metastases in women with advanced breast cancer.
本研究的目的是确定双膦酸盐氯膦酸盐对晚期乳腺癌女性骨转移发生率及相关发病率的影响。133例复发性乳腺癌但无骨转移证据的女性,在英国和加拿大的两个临床肿瘤中心,在双盲条件下被随机分配,每天口服1600毫克氯膦酸盐或相同的安慰剂,为期3年。主要观察指标包括通过连续骨扫描和X线片判断的骨转移发生情况,以及与骨转移相关的发病率,包括高钙血症、椎体和非椎体骨折的发生率,以及根据骨放疗需求评估的骨痛。氯膦酸盐治疗组发生骨转移的患者数量低于安慰剂组(15例对19例),但差异无统计学意义。氯膦酸盐治疗组的骨转移数量显著低于安慰剂组(32例对63例;p<0.005)。与对照组相比,氯膦酸盐治疗组骨病并发症减少26%(p<0.01)。与安慰剂相比,氯膦酸盐对椎体畸形(29%)和非椎体骨折(75%)有显著疗效,但每种情况的事件发生率较低。对放疗需求和高钙血症(39%)有较小(22%)但无统计学意义的治疗效果。氯膦酸盐对生存率无影响。我们得出结论,口服氯膦酸盐可显著降低晚期乳腺癌女性骨转移的数量和并发症。