首页> 外文期刊>British Journal of Cancer >Oral ibandronate reduces the risk of skeletal complications in breast cancer patients with metastatic bone disease: results from two randomised, placebo-controlled phase III studies
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Oral ibandronate reduces the risk of skeletal complications in breast cancer patients with metastatic bone disease: results from two randomised, placebo-controlled phase III studies

机译:口服伊班膦酸可降低患有转移性骨病的乳腺癌患者发生骨骼并发症的风险:两项随机,安慰剂对照的III期研究的结果

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Although intravenous (i.v.) bisphosphonates are the standard of care for metastatic bone disease, they are less than ideal for many patients due to infusion-related adverse events (AEs), an increased risk of renal toxicity and the inconvenience of regular hospital visits. The use of oral bisphosphonate therapy is limited by concerns over efficacy and gastrointestinal (GI) side effects. There remains a clinical need for an oral bisphosphonate that offers equivalent efficacy to i.v. bisphosphonates, good tolerability and dosing convenience. Oral ibandronate, a highly potent, third-generation aminobisphosphonate, has been evaluated in phase III clinical trials of patients with bone metastases from breast cancer. In two pooled phase III studies, patients with breast cancer and bone metastases were randomised to receive oral ibandronate 50?mg (n=287) or placebo (n=277) once daily for up to 96 weeks. The primary end point was the skeletal morbidity period rate (SMPR), defined as the number of 12-week periods with new skeletal complications. Multivariate Poisson's regression analysis was used to assess the relative risk of skeletal-related events in each treatment group during the study period. Oral ibandronate 50?mg significantly reduced the mean SMPR compared with placebo (0.95 vs 1.18, P=0.004). There was a significant reduction in the mean number of events requiring radiotherapy (0.73 vs 0.98, Pvs 0.53, P=0.037). Poisson's regression analysis confirmed that oral ibandronate significantly reduced the risk of a skeletal event compared with placebo (hazard ratio 0.62, 95% CI=0.48, 0.79; P=0.0001). The incidence of mild treatment-related upper GI AEs was slightly higher in the oral ibandronate 50?mg group compared with placebo, but very few serious drug-related AEs were reported. Oral ibandronate 50?mg is an effective, well-tolerated and convenient treatment for the prevention of skeletal complications of metastatic bone disease.
机译:尽管静脉内(i.v.)双膦酸盐是转移性骨疾病的标准治疗方法,但由于输液相关的不良事件(AE),肾毒性风险增加以及定期就诊不便,它们对许多患者而言并不理想。对功效和胃肠道(GI)副作用的关注限制了口服双膦酸盐疗法的使用。临床上仍需要口服双膦酸盐,其具有与静脉内注射相同的功效。双膦酸酯,良好的耐受性和给药方便性。口服伊班膦酸盐是一种高效的第三代氨基双膦酸盐,已在患有乳腺癌的骨转移患者的III期临床试验中进行了评估。在两项合并的III期研究中,患有乳腺癌和骨转移的患者被随机分配接受口服伊班膦酸50?mg(n = 287)或安慰剂(n = 277),每天一次,长达96周。主要终点是骨骼发病率(SMPR),定义为新骨骼并发症的12周周期数。在研究期间,使用多元Poisson回归分析评估每个治疗组中与骨骼相关事件的相对风险。与安慰剂相比,口服伊班膦酸50mg显着降低了平均SMPR(0.95比1.18,P = 0.004)。需要放疗的平均事件数显着减少(0.73比0.98,Pvs 0.53,P = 0.037)。 Poisson回归分析证实,与安慰剂相比,口服伊班膦酸酯显着降低了发生骨骼事件的风险(危险比0.62,95%CI = 0.48,0.79; P = 0.0001)。与安慰剂相比,口服伊班膦酸50 mg组与轻度治疗相关的上消化道AE的发生率稍高,但很少报道严重的与药物相关的AE。口服伊班膦酸50毫克是一种有效,耐受良好且方便的治疗方法,可预防转移性骨病的骨骼并发症。

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