University of Alabama at Birmingham.
Amgen Inc., Thousand Oaks, California.
Arthritis Rheumatol. 2019 Jul;71(7):1174-1184. doi: 10.1002/art.40874. Epub 2019 May 25.
Clinical trial results have shown that, in glucocorticoid-treated patients, treatment with denosumab 60 mg subcutaneously once every 6 months (Q6M) increased spine and hip bone mineral density (BMD) at month 12 significantly more than treatment with risedronate 5 mg orally once daily (QD). The present analysis was performed to compare efficacy and characterize safety through month 24.
This phase III study enrolled men and women ≥18 years old who had received ≥7.5 mg daily prednisone or equivalent for <3 months (glucocorticoid-initiating) or for ≥3 months (glucocorticoid-continuing) before screening. All patients <50 years old had a history of osteoporotic fracture. Glucocorticoid-continuing patients ≥50 years old had T scores of -2.0 or less (or -1.0 or less with fracture history). Patients were randomized (1:1) to receive denosumab 60 mg subcutaneously Q6M or risedronate 5 mg orally QD for 24 months, with daily calcium and vitamin D.
Of 795 patients, 590 (74.2%) completed the study (in the glucocorticoid-initiating group, 109 of 145 patients treated with denosumab and 117 of 145 patients treated with risedronate; in the glucocorticoid-continuing group, 186 of 253 patients treated with denosumab and 178 of 252 patients treated with risedronate). Denosumab was superior to risedronate in increasing lumbar spine and total hip BMD at all time points assessed, among glucocorticoid-initiating patients (24-month lumbar spine: BMD increase of 6.2% versus 1.7%, respectively [P < 0.001]; 24-month total hip: BMD increase of 3.1% versus 0.0% [P < 0.001]) and among glucocorticoid-continuing patients (24-month lumbar spine: BMD increase of 6.4% versus 3.2% [P < 0.001]; 24-month total hip: BMD increase of 2.9% versus 0.5% [P < 0.001]). Adverse events, serious adverse events (including infections), and fractures were similar between treatment groups.
Denosumab was superior to risedronate in terms of increases in spine and hip BMD through month 24, and the safety profile was similar between treatment groups. Denosumab may offer a new osteoporosis treatment option for glucocorticoid-treated patients.
临床试验结果表明,在接受糖皮质激素治疗的患者中,与每日口服利塞膦酸钠 5 毫克(QD)相比,每 6 个月皮下注射地舒单抗 60 毫克(Q6M)可显著增加第 12 个月时的脊柱和髋部骨密度(BMD)。本分析旨在比较 24 个月时的疗效和安全性特征。
这项 III 期研究纳入了年龄≥18 岁的男性和女性患者,他们在筛选前接受了<3 个月(起始糖皮质激素组)或≥3 个月(持续糖皮质激素组)的每日泼尼松或等效剂量的治疗。所有<50 岁的患者均有骨质疏松性骨折史。≥50 岁的持续糖皮质激素组患者的 T 评分≤-2.0(或有骨折史的患者 T 评分≤-1.0)。患者被随机(1:1)皮下注射地舒单抗 60 毫克 Q6M 或口服利塞膦酸钠 5 毫克 QD 治疗 24 个月,同时每日补充钙和维生素 D。
在 795 例患者中,590 例(74.2%)完成了研究(在起始糖皮质激素组中,接受地舒单抗治疗的 145 例患者中有 109 例,接受利塞膦酸钠治疗的 145 例患者中有 117 例;在持续糖皮质激素组中,接受地舒单抗治疗的 253 例患者中有 186 例,接受利塞膦酸钠治疗的 252 例患者中有 178 例)。在起始糖皮质激素组患者中(24 个月时的腰椎骨密度:BMD 增加分别为 6.2%和 1.7%,差异有统计学意义(P<0.001);24 个月时的全髋骨密度:BMD 增加分别为 3.1%和 0.0%,差异有统计学意义(P<0.001))和持续糖皮质激素组患者中(24 个月时的腰椎骨密度:BMD 增加分别为 6.4%和 3.2%,差异有统计学意义(P<0.001);24 个月时的全髋骨密度:BMD 增加分别为 2.9%和 0.5%,差异有统计学意义(P<0.001)),地舒单抗在增加脊柱和髋部 BMD 方面优于利塞膦酸钠。两组患者的不良事件、严重不良事件(包括感染)和骨折发生率相似。
在 24 个月时,地舒单抗在增加脊柱和髋部 BMD 方面优于利塞膦酸钠,且两组的安全性特征相似。地舒单抗可能为接受糖皮质激素治疗的患者提供一种新的骨质疏松症治疗选择。