Introduction
Osteoporosis is characterized by reduced bone mineral density (BMD), increased microstructural deterioration, and, consequently, increased fracture risk. Worldwide, approximately 9 million new osteoporotic fractures occur per year, including 1.7 million fractures of the forearm, 1.6 million fractures of the hip, and 1.4 million clinical vertebral fractures [
1]. Wrist fractures are the most common nonvertebral fractures in postmenopausal women with osteoporosis, particularly in elderly women [
2‐
5]. Individuals with wrist fractures may experience chronic loss of function [
6] and reduced quality of life [
5]. Furthermore, wrist fractures are associated with significant morbidity [
2‐
4] and may be associated with increased mortality, especially in men [
7,
8]. Forearm, wrist, and humerus fractures have also been shown to predict subsequent vertebral, hip, wrist, and forearm fractures [
9‐
13].
Data on currently available therapies are limited with regard to treatment effects on wrist fractures and corresponding changes in BMD. Studies of alendronate have shown both significant [
14] and nonsignificant [
15] reductions in wrist fractures compared with placebo. Studies have also shown that bisphosphonates maintain reductions in BMD at the distal radius compared with baseline, especially at the 1/3 radius, which is primarily cortical bone [
16‐
19]. Studies of teriparatide have shown both significant decreases in wrist fractures [
20] and significant reductions in wrist BMD [
21] compared with placebo. Thus, previous reports of osteoporosis medications do not present a clear association between changes in BMD and fracture risk at the wrist.
In contrast to other antiresorptive therapies, denosumab—a fully human monoclonal antibody against RANK ligand (RANKL)—increases BMD at the 1/3 radius, as determined by dual-energy X-ray absorptiometry (DXA), more than alendronate not only in bisphosphonate treatment-naïve patients [
22] but also in previously bisphosphonate-treated patients [
23]. Denosumab also enhances BMD at the 1/3 radius more than zoledronic acid in patients previously treated with long-term alendronate [
24]. In a phase 2 study, denosumab reduced bone resorption more rapidly and decreased cortical porosity more than alendronate [
17].
While denosumab was not shown to reduce wrist fractures in the overall study population of the FREEDOM study [
25,
26], improvements in bone mass, density, and strength [
18] with denosumab treatment have been associated with reductions in wrist fractures among women at higher risk, defined as having a femoral neck BMD T-score ≤ − 2.5 [
26]. Long-term experience with denosumab provides further support for the relationship between increases in BMD and reductions in nonvertebral fracture risk [
27,
28].
No study has assessed the effect of treatment on long-term (> 3 years) forearm BMD changes and the risk of upper limb fractures (i.e., wrist, forearm, and humerus). With this objective, we evaluated the long-term effects of denosumab treatment on changes in forearm BMD by DXA and their relationship with fracture incidence at three different upper limb sites. We used data from the cross-over group of subjects from the FREEDOM Extension trial, who received 3 years of placebo followed by up to 7 years of denosumab. The results provide further evidence for the beneficial effects of denosumab at both cortical and trabecular compartments of the bone, leading to reductions in the risk of upper limb fractures.
Methods
Study design
The 3-year FREEDOM trial (NCT00089791) and its 7-year Extension (NCT00523341) have been described previously [
25,
28]. Briefly, FREEDOM was a phase 3, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of denosumab in postmenopausal women with osteoporosis. Subjects were randomized to receive either placebo or denosumab 60 mg subcutaneously (SC) every 6 months (Q6M) for 3 years. Subjects were instructed to take calcium (≥ 1 g) and vitamin D (≥ 400 IU) daily. Subjects who completed the FREEDOM trial, did not discontinue investigational product, and did not miss > 1 dose of investigational product were eligible to enter a 7-year Extension trial. During the Extension, all subjects were to receive open-label denosumab 60 mg SC Q6M, with daily calcium and vitamin D.
This analysis evaluated subjects who were randomized to receive placebo for 3 years in the FREEDOM, entered the Extension study, and received denosumab for up to 7 years (i.e., the cross-over group). The cross-over group was chosen because it provided fracture rates during the placebo period, which was used for within-group comparisons. Fracture rates at the wrist, forearm, humerus, and all upper limb fractures together were assessed in all subjects from the cross-over group. A subset of subjects from the cross-over group also participated in a BMD substudy, in which forearm BMD was measured. This substudy was prespecified in both the FREEDOM and Extension trial protocols.
Study population
Subjects who were randomized to placebo in the FREEDOM and received up to 7 years of denosumab in the Extension were included in this analysis. Subject inclusion and exclusion criteria have been described previously [
28]. Women between the age of 60 and 90 years with a lumbar spine or total hip BMD T-score ≤ − 2.5 at either site but > − 4.0 at both sites were eligible for the FREEDOM trial.
Outcome measures
BMD assessments were performed by DXA. DXA measurements were obtained by Lunar or Hologic instruments (GE Healthcare, Chicago, IL, or Hologic Inc., Marlborough, MA, respectively). All DXA scans were analyzed centrally by Synarc (Portland, OR) in a blinded fashion. During the 10-year course of FREEDOM and its Extension, the central laboratory made appropriate adjustments upon each change in software to ensure consistency of BMD results. Ultradistal radius, 1/3 radius, and total radius DXA measurements were recorded for a subset of subjects at FREEDOM baseline, during FREEDOM (years 1–3), and during FREEDOM Extension (years 1–3, 5, and 7). Wrist, forearm, humerus, and upper limb (combined wrist, forearm, and humerus) fracture rates were confirmed by a central imaging vendor for all subjects through year 3 in the FREEDOM study and through year 7 of FREEDOM Extension. Fractures of interest by site were defined in the following manner: wrist fractures included fractures at the distal radius and distal ulna; forearm fractures included fractures at the proximal radius/ulna, shaft radius/ulna, and distal radius/ulna; humerus fractures included fractures at the proximal humerus, shaft humerus, and distal humerus; and upper limb fractures included fractures at the forearm and humerus. Traumatic and pathologic fractures were excluded. Changes in BMD and fracture rates were evaluated in three time periods to allow for within-group comparisons—FREEDOM years 1–3, Extension years 1–3, and Extension years 4–7—to evaluate patients after they received 3 years of placebo, 3 years of denosumab, and 4 additional years of denosumab, respectively. Fracture rates were compared between either the first 3 years on denosumab or the subsequent last 4 years on denosumab with the first 3 years on placebo to assess the effect of denosumab treatment on fracture rates. To adjust for various lengths of follow-up, fracture rates were expressed as per 100 subject-years. Rate ratios were used for within-group comparison between placebo and denosumab treatment periods. Fracture rates and changes in BMD are also reported for the long-term group (i.e., subjects randomized to receive denosumab during FREEDOM, entered the Extension, and received denosumab for up to an additional 7 years), to compare with those observed in the cross-over group during the same period of denosumab treatment in the Extension (i.e., the first 3 years and following 4 years of denosumab treatment).
Statistical analyses
Baseline demographic and disease characteristic values were summarized using descriptive statistics. The percentage change from FREEDOM baseline and Extension baseline in BMD at the ultradistal radius, 1/3 radius, and total radius by visit (during the FREEDOM and its Extension) was analyzed using a repeated-measures mixed-effects model with an unstructured within-subject variance-covariance structure. The model included treatment, visit (categorical), baseline BMD value, age stratification variable, densitometry machine type, treatment-by-visit interaction, and BMD baseline value-by-densitometry machine-type interaction. Least squares mean estimates of the percentage change from baseline in BMD within each treatment group and by visit, and the corresponding two-sided 95% confidence intervals (CIs), were estimated. Wrist, forearm, humerus, and upper limb fracture rates (per 100 subject-years) were computed, and the rate ratios (comparing FREEDOM Extension years 1–3 or 4–7 with placebo FREEDOM years 1–3 and comparing FREEDOM Extension years 4–7 with FREEDOM Extension years 1–3) and the corresponding 95% CIs were estimated by generalized estimating equation method in a Poisson regression model. All p values were not adjusted for multiplicity.
Discussion
The objective of this study was to evaluate the long-term treatment effect of denosumab on fracture risk of the upper limb and the associated changes in BMD at the forearm, including ultradistal radius, 1/3 radius, and total radius sites. During FREEDOM Extension, long-term denosumab treatment significantly decreased the risk of upper limb fractures, including wrist, forearm, and humerus, which was associated with a complete reversal of bone loss observed during the first 3 years of FREEDOM, when these patients received only calcium and vitamin D supplementation.
Upper limb fractures account for about one-third of all osteoporosis-related fractures in the elderly and are associated with significant morbidity and mortality [
4,
8] and loss of quality of life [
5]. The present study is the first to examine the long-term effect of osteoporosis treatment on upper limb fractures, indicating that 7 years of denosumab treatment was associated with a significant 48% reduction in the risk of all upper limb fractures and a 43%, 43%, and 58% reduction in risk of forearm, wrist, and humerus fractures, respectively, compared with placebo treatment during FREEDOM. Fracture risk reduction with denosumab, however, was not evident during the first 3 years of treatment during the Extension but rather during the last 4 years of treatment, with the exception of the humerus, where a 55% reduction was observed within the first 3 years of denosumab treatment and sustained through 7 years of treatment. It is unclear why the humerus appears to respond earlier to denosumab treatment than the wrist and forearm. While findings from the FREEDOM study demonstrated a significant reduction in nonvertebral fractures with 3 years of denosumab treatment compared with placebo [
25], this current longitudinal analysis suggests that reduction of upper limb fractures may require more than 3 years of therapy because cortical bone is relatively slow to react to an antiresorptive, particularly at a relatively low load site with little—if any—modeling-based bone formation [
30]. It should be mentioned that by the end of the 7-year Extension period, patients were older and, thus, at higher fracture risk compared with the first 3 years of FREEDOM, potentially underestimating the fracture risk reduction observed with denosumab treatment in this longitudinal study without a parallel comparator arm. Our findings indicate that denosumab effectively reduces fractures in the upper limb, including the wrist and humerus, with important clinical implications. Recent recommendations from the National Bone Health Alliance expanded the diagnosis of osteoporosis to include fractures at the proximal humerus and, in some cases, distal forearm in patients with osteopenic BMD [
31].
Although some studies have shown a reduction in wrist fractures with alendronate treatment [
14,
32], others have shown neither a reduction in wrist fractures nor an increase in wrist BMD [
15,
19]. A Cochrane review showed an overall relative risk reduction of about 50% for wrist fractures with alendronate treatment [
33]. No studies have reported the effect of antiresorptive agents on other upper limb fractures.
Among available osteoporosis therapies, reduction in vertebral fracture risk is a consistent finding that becomes evident relatively early in the course of treatment. In addition, the size of the treatment effect on vertebral fractures is greater than that on nonvertebral fractures. Reductions in nonvertebral fractures, including at the upper extremities, are less pronounced with antiresorptive therapies and appear to require a longer treatment duration. Treatment with denosumab results in reductions in vertebral fractures after 1 year, whereas reductions in nonvertebral fractures occur after 3 years. Longer term denosumab treatment beyond 3 years has been shown to be associated with further reductions in nonvertebral fractures [
27]. This long-term, beneficial treatment effect is thought to be derived not only from the increase in bone mass but also from reductions in cortical porosity and increases in cortical thickness and strength documented at nonvertebral sites, including the distal radius, tibia, and hip [
17,
34].
In contrast, longer treatment with alendronate for up to 10 years [
35] or zoledronic acid for up to 9 years [
36] was not associated with further reductions in nonvertebral fractures compared with the first 3 years of each respective treatment. This may be explained by the differing effects of denosumab and alendronate on cortical bone [
17], as well as the differing effects on femoral neck BMD that plateaus after 2–3 years of treatment with bisphosphonates. To inhibit resorption, bisphosphonates must first be adsorbed to hydroxyapatite bone mineral surfaces—more abundantly expressed on trabecular bone than cortical—underneath the osteoclasts, and then later be taken up by osteoclasts during resorption [
16]. Thus, some resorption must occur before bisphosphonates can inhibit osteoclastic activity. Furthermore, bisphosphonates do not prevent osteoclastogenesis. By contrast, denosumab, a fully human monoclonal antibody against RANKL that does not require binding to bone mineral surfaces, reduces osteoclastogenesis and bone resorption more completely and rapidly than bisphosphonates and may penetrate deeper into cortical bone [
16]. These differences in mechanisms of action may confer larger effects of denosumab compared with alendronate on cortical bone [
17].
The strength of this study is that it reports long-term, 10-year changes in BMD at three sites of interest at the radius. The fracture risk reduction calculations were based on a large sample size, i.e., all subjects randomized to placebo in the FREEDOM trial who entered the Extension. In addition, the 7 years of denosumab treatment in the cross-over group could be compared with the first 7 years of denosumab treatment in the long-term group; those findings show similar outcomes, demonstrating that longer term denosumab treatment (beyond 3 years) further decreases fracture risk. The limitation of this study is the relatively small number of subjects who participated in the BMD substudy; however, as baseline characteristics were similar between the subjects enrolled in the overall cross-over group and in the BMD substudy, the subjects investigated appear to be representative of the overall study population. DXA does not measure humeral BMD, so it is not possible to associate reductions in humerus fracture rates with increases in BMD at that skeletal site. This study is also limited by the open-label, single-arm design of the Extension trial and the lack of a placebo group.
In conclusion, compared with the initial 3 years of treatment with calcium and vitamin D supplements during the FREEDOM trial, 7 years of denosumab treatment decreased the incidence of upper limb fractures, including those at the wrist, humerus, and forearm. The beneficial effect of denosumab treatment on fractures was associated with significant increases in BMD over the 7-year course of therapy compared with Extension baseline and complete reversal of the bone loss observed during the first 3 years of the FREEDOM trial. This study also suggests that for some nonvertebral skeletal sites, such as the upper limb, a treatment duration of more than 3 years results in significant and clinically meaningful treatment effect. Considering the reversibility of denosumab, as well as its long-term safety and proven efficacy, continued treatment with a drug holiday is a very important consideration. These findings support the treatment benefits of long-term therapy with potent antiresorptive agents, such as denosumab, and their importance in enabling a patient to maintain one’s independence, activity level, and overall quality of life.
Compliance with ethical standards
Conflict of interest
JP Bilezikian has received research grants from the National Institutes of Health and has received consulting fees from Amgen, Radius, Ultragenyx, Alexion, and Shire. CJF Lin is a former employee and stockholder of Amgen Inc. JP Brown has received research grants from Amgen Inc., Eli Lilly, and Mereo BioPharma; received consulting fees from Amgen Inc., Eli Lilly, and Merck; and served on the speakers’ bureau for Amgen Inc. and Eli Lilly. AT Wang, X Yin, and A Chines are employees and stockholders of Amgen Inc. P Ebeling has received research grants from Amgen Inc., Eli Lilly, Novartis, and Alexion, and has received consulting fees from Amgen Inc., Eli Lilly, Alexion, and Gilead. A Fahrleitner-Pammer has received consulting fees from Eli Lilly and has served on the speakers’ bureau for Alexion, Amgen Inc., Eli Lilly, and Stada. E Franek has served on the speakers’ bureau for Amgen Inc., Eli Lilly, and MSD. N Gilchrist has received research grants from Amgen Inc. PD Miller has received research grants from Amgen Inc., Alexion, Radius Pharma, and Regeneron. JA Simon has received research grants from AbbVie Inc., Allergan Plc, Agile Therapeutics, Bayer Healthcare LLC., Dornier MedTech, Endoceutics Inc., GTx, Inc., Ipsen, Myovant Sciences, New England Research Institute Inc., ObsEva SA, Palatin Technologies, Symbio Research Inc., TherapeuticsMD, and Tissue Genesis; has ownership in James A. Simon, MD, PC; has received consulting fees from AbbVie Inc., Allergan Plc, AMAG Pharmaceuticals Inc., Amgen Inc., Ascend Therapeutics, Bayer HealthCare Pharmaceuticals Inc., CEEK Enterprises LLC., Covance Inc., Millendo Therapeutics Inc., Mitsubishi Tanabe Pharma Development America Inc., ObsEva SA, Radius Health Inc., Sanofi S.A., Sebela Pharmaceuticals Inc., Shionogi Inc., Symbiotec Pharmalab, TherapeuticsMD, and Valeant Pharmaceuticals; has served on the speakers’ bureau for AMAG Pharmaceuticals Inc., Duchesnay USA, Novo Nordisk, Shionogi Inc., and Valeant Pharmaceuticals; and is a stockholder in Sermonix Pharmaceuticals. I Valter has nothing to disclose. CAF Zerbini has received research grants from Pfizer, Amgen Inc., Sanofi, MSD, Novartis, and Lilly, and has served on the speakers’ bureau for Pfizer, Lilly, and Sanofi. C Libanati is an employee and stockholder of UCB Pharma.
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