Hortobagyi G N, Theriault R L, Lipton A, Porter L, Blayney D, Sinoff C, Wheeler H, Simeone J F, Seaman J J, Knight R D, Heffernan M, Mellars K, Reitsma D J
Department of Breast Medical Oncology, University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.
J Clin Oncol. 1998 Jun;16(6):2038-44. doi: 10.1200/JCO.1998.16.6.2038.
Pamidronate, an aminobisphosphonate, has been shown to lower the risk of skeletal complications associated with lytic bone lesions for up to 1 year in women with stage IV breast cancer who received chemotherapy. We studied the long-term effectiveness and safety of continued treatment with intravenous pamidronate infusions for up to 2 years.
Three hundred eighty-two women with metastatic breast cancer and lytic bone lesions who received chemotherapy were randomly assigned to receive either 90 mg of pamidronate or placebo intravenously every 3 to 4 weeks in this double-blind, multicenter, parallel-group trial. Patients were evaluated monthly for 2 years for skeletal complications, which included pathologic fractures, need for radiation or surgery to treat bone complications, spinal cord compression, and hypercalcemia. Bone pain, analgesic use, bone biochemical markers, performance status, quality of life, radiologic response in bone, and survival were also evaluated.
As in the first year of treatment, the proportion of patients with any skeletal complication was significantly less for the pamidronate than the placebo group at 15, 18, 21, and 24 months (P < .001). The proportions of patients with any pathologic fracture (i.e., vertebral and nonvertebral fractures), need for radiation or surgery to treat bone complications, and hypercalcemia were also statistically less for the pamidronate than the placebo group. The median time to the first skeletal complication was 13.9 months in the pamidronate-treated women and 7.0 months in the placebo group (P < .001). Long-term treatment did not result in any unexpected adverse events. Survival did not differ between the two groups.
The risk for osteolytic bone lesion complications in metastatic breast cancer was significantly decreased with monthly infusions of 90 mg of pamidronate, and this effect was maintained for at least 2 years. Pamidronate is a useful adjunct to standard chemotherapy in the palliative treatment of metastatic breast cancer.
帕米膦酸盐是一种氨基双膦酸盐,已证明在接受化疗的IV期乳腺癌女性中,可降低与溶骨性骨病变相关的骨骼并发症风险长达1年。我们研究了静脉输注帕米膦酸盐持续治疗长达2年的长期有效性和安全性。
在这项双盲、多中心、平行组试验中,382例接受化疗且有转移性乳腺癌和溶骨性骨病变的女性被随机分配,每3至4周静脉注射90毫克帕米膦酸盐或安慰剂。对患者进行为期2年的每月评估,以检查骨骼并发症,包括病理性骨折、治疗骨并发症所需的放疗或手术、脊髓压迫和高钙血症。还评估了骨痛、止痛药物使用、骨生化标志物、体能状态、生活质量、骨的放射学反应和生存率。
与治疗的第一年一样,在第15、18、21和24个月时,帕米膦酸盐组发生任何骨骼并发症的患者比例显著低于安慰剂组(P < .001)。帕米膦酸盐组发生任何病理性骨折(即椎体和非椎体骨折)、因骨并发症需要放疗或手术以及高钙血症的患者比例在统计学上也低于安慰剂组。接受帕米膦酸盐治疗的女性首次发生骨骼并发症的中位时间为13.9个月,安慰剂组为7.0个月(P < .001)。长期治疗未导致任何意外不良事件。两组生存率无差异。
每月输注90毫克帕米膦酸盐可显著降低转移性乳腺癌中溶骨性骨病变并发症的风险,且这种效果至少维持2年。帕米膦酸盐是转移性乳腺癌姑息治疗中标准化疗的有用辅助药物。