GRAND-4: the German retrospective analysis of long-term persistence in women with osteoporosis treated with bisphosphonates or denosumab

被引:38
作者
Hadji, P. [1 ]
Kyvernitakis, I. [2 ]
Kann, P. H. [3 ]
Niedhart, C.
Hofbauer, L. C. [4 ,5 ]
Schwarz, H.
Kurth, A. A. [6 ]
Thomasius, F. [7 ]
Schulte, M. [8 ]
Intorcia, M. [9 ]
Psachoulia, E. [9 ]
Schmid, T. [9 ]
机构
[1] Krankenhaus NW Frankfurt, Dept Bone Oncol Endocrinol & Reprod Med, Steinbacher Hohl 2-26, D-60488 Frankfurt, Germany
[2] Nordwest Hosp, Dept Bone Oncol Gynecol Endocrinol & Reprod Med, Frankfurt, Germany
[3] Univ Marburg, Ctr Internal Med Endocrinol & Diabet, Marburg, Germany
[4] TU Dresden Med Ctr, Div Endocrinol Diabet & Bone Dis, Dept Med 3, Dresden, Germany
[5] TU Dresden Med Ctr, Ctr Hlth Aging, Dresden, Germany
[6] Themistocles Gluck Hosp, Ratingen, Germany
[7] Krankenhaus NW Frankfurt, Dept Bone Oncol & Osteoporosis Ctr, Frankfurt, Germany
[8] Amgen Europe GmbH, Munich, Germany
[9] Amgen Europe, Zug, Switzerland
关键词
Bisphosphonates; Compliance; Denosumab; Osteoporosis; Persistence; POSTMENOPAUSAL WOMEN; FRACTURE RISK; ORAL BISPHOSPHONATES; COST-EFFECTIVENESS; BONE TURNOVER; ADHERENCE; SATISFACTION; ALENDRONATE; THERAPY; MEDICATIONS;
D O I
10.1007/s00198-016-3623-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This retrospective database study assessed 2-year persistence with bisphosphonates or denosumab in a large German cohort of women with a first-time prescription for osteoporosis treatment. Compared with intravenous or oral bisphosphonates, 2-year persistence was 1.5-2 times higher and risk of discontinuation was significantly lower (P < 0.0001) with denosumab. Persistence with osteoporosis therapies is critical for fracture risk reduction. Detailed data on long-term persistence (aeyen2 years) with bisphosphonates and denosumab are sparse. From the German IMSA (R) database, we included women aged 40 years or older with a first-time prescription for bisphosphonates or denosumab between July 2010 and August 2014; patients were followed up until December 2014. The main outcome was treatment discontinuation, with a 60-day permissible gap between filled prescriptions. Two-year persistence was estimated using Kaplan-Meier survival curves, with treatment discontinuation as the failure event. Denosumab was compared with intravenous (i.v.) and oral bisphosphonates separately. Cox proportional hazard ratios (HRs) for the 2-year risk of discontinuation were calculated, with adjustment for age, physician specialty, health insurance status, and previous medication use. Two-year persistence with denosumab was significantly higher than with i.v. or oral bisphosphonates (39.8 % [n = 21,154] vs 20.9 % [i.v. ibandronate; n = 20,472] and 24.8 % [i.v. zoledronic acid; n = 3966] and 16.7-17.5 % [oral bisphosphonates; n = 114,401]; all P < 0.001). Patients receiving i.v. ibandronate, i.v. zoledronic acid, or oral bisphosphonates had a significantly increased risk of treatment discontinuation than did those receiving denosumab (HR = 1.65, 1.28, and 1.96-2.02, respectively; all P < 0.0001). Two-year persistence with denosumab was 1.5-2 times higher than with i.v. or oral bisphosphonates, and risk of discontinuation was significantly lower with denosumab than with bisphosphonates. A more detailed understanding of factors affecting medication-taking behavior may improve persistence and thereby reduce rates of fracture.
引用
收藏
页码:2967 / 2978
页数:12
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