Baseline Characteristics and Changes in Bone Mineral Density T-Scores of Bulgarian Women with Postmenopausal Osteoporosis Receiving Denosumab in Routine Clinical Practice

Abstract

Background

Postmenopausal osteoporosis (PMO) is common among women over 50 years of age and is associated with an increased risk of fracture. Bone-targeted agents, such as denosumab, can reduce fracture risk in patients with PMO.

Objective

The aim was to describe baseline characteristics and changes in bone mineral density (BMD) T-scores among women with PMO receiving denosumab in Bulgaria.

Methods

This multicenter chart review included women with PMO receiving denosumab for ≥1 year in Bulgaria (October 2011–August 2013). Participants were required to have a baseline BMD T-score of ≤−2.5 standard deviations (SDs) at one or more skeletal sites.

Results

Overall, 222 women were included. The mean (SD) age at denosumab initiation was 64.2 (8.5) years; 26.6% reported a previous osteoporotic fracture and 6.8% a previous hip fracture. Only half of those reporting a previous fracture (49.2%) had received prior osteoporosis therapy. At baseline, mean (SD) BMD T-scores were lumbar spine −3.2 SD (0.6 SD), total hip −2.3 SD (0.8 SD), and femoral neck −2.7 SD (0.7 SD). After 1 year of denosumab treatment, scores increased significantly at all three sites, reaching −2.7 SD (0.6 SD), −2.1 SD (0.9 SD), and −2.4 SD (0.7 SD), respectively (all p < 0.0001 vs. baseline). No serious adverse drug reactions were identified.

Conclusion

Denosumab is usually prescribed in women with PMO at high fracture risk. In the patients who were persistent with treatment at 1 year, denosumab was well tolerated and effective at increasing BMD T-scores at several skeletal sites.

Key Points

This study reviewed the medical records of women receiving denosumab for the treatment of postmenopausal osteoporosis in Bulgaria.

The characteristics of the women suggest that they were at high risk of fracture before they were prescribed denosumab.

Denosumab increased bone mineral density after 1 year of treatment, which may help to reduce the risk of fractures in this patient population.

Introduction

Osteoporosis is characterized by low bone mineral density (BMD) and microarchitectural deterioration of bone tissue, which leads to an increased risk of fracture [1]. It has been estimated that 21% of women aged 50–84 years had osteoporosis worldwide in 2010 and that approximately 22 million women in Europe were affected [2]. These findings are similar to those of the largest epidemiologic osteoporosis study in Bulgaria, in which 16.8% of women aged 50 years or older were found to have osteoporosis at the femoral neck (FN) [3].

Fragility fractures are common in women over the age of 50 years, and the risk of fracture correlates with increasing age and decreasing BMD T-score [4, 5]. In Bulgaria, the mean 10-year absolute fracture risk for women with osteoporosis is reported to be 13.4% for major fractures and 2.8% for hip fractures [3]. The risk of major fractures was 8.8% in patients aged 50–59 years versus 19.6% in those aged 70 years and over, while the risk of hip fractures in these age groups was 1.0 and 6.5%, respectively. Over one-fifth (23.3%) of women reported previous low-trauma fractures, including those affecting the wrist (9.1% of low-trauma fractures), hip (1.9%), and vertebrae (2.3%) [3]. Indeed, Svedbom et al. estimated that in the 1.6 million women aged 50 years or older in Bulgaria, 21,476 fractures might have occurred in 2010 [6]. However, data from the UK and Australia suggest that up to one-half of all vertebral fractures may go unrecognized [7, 8].

It has been estimated that, in Bulgaria in 2010, 7197 quality-adjusted life-years were lost in women aged over 50 years owing to osteoporotic fractures [6] and that the cost burden of osteoporosis was €42 million [6]. Overall, hip fractures were estimated to be the most expensive type of fracture (€20 million), with the cost per fracture in 2010 estimated at €1826 [6].

Denosumab, a fully-human monoclonal antibody (IgG2) against RANK ligand (RANKL), was approved in Europe in 2010 for the treatment of osteoporosis in patients with an increased risk of fractures [9, 10]. Denosumab binds RANKL with high affinity and specificity, preventing activation of its cognate receptor RANK that is expressed on the surface of osteoclasts and osteoclast precursors. Inhibition of signaling through the RANK receptor prevents osteoclast maturation, activation and survival, thereby decreasing bone resorption in cortical and trabecular bone [9]. An in vivo animal study showed that inhibition of bone resorption with denosumab improved the structural strength of bone [11, 12]. Treatment with denosumab has been associated with significant reductions in fracture risk across a wide range of patient groups [10, 13, 14]. Furthermore, long-term clinical trial follow-up data from the phase III Fracture REduction Evaluation of Denosumab in Osteoporosis every 6 months (FREEDOM) extension study demonstrated that denosumab treatment for up to 10 years was associated with a persistent reduction of bone turnover, continued increases in BMD, without therapeutic plateau, and a low fracture incidence [15]. As a consequence, Bulgarian guidelines recommend denosumab [60-mg subcutaneous injection every 6 months (SC Q6M)] as a first-line therapy to reduce the risk of vertebral, non-vertebral, and hip fractures in women with postmenopausal osteoporosis (PMO) [16].

It is of great interest to examine the profiles of patients who receive denosumab in real-world clinical practice; however, currently, such data are sparse. This study describes the baseline characteristics and changes in BMD T-scores among women with PMO who have received at least two injections of denosumab in Bulgarian clinical practice. This information may help to identify women with PMO who could gain the most benefit from treatment with denosumab.

Methods

Study Design

This retrospective, observational, multicenter chart review planned to include 200 women from ten representative osteoporosis practices in Bulgaria. The study protocol was approved by a central regulatory agency ethics committee, in accordance with the ethical principles of the Declaration of Helsinki.

Participants

Women were considered eligible for inclusion if they were aged 50 years or older, had a densitometric diagnosis of PMO [BMD T-score ≤−2.5 standard deviations (SDs) at one or more skeletal sites], had initiated denosumab (60 mg SC Q6M) in or after October 2011, and had received a second injection before the end of the study period (August 2013). After enrollment, patients were excluded if they had not received their second injection within 7 months of the first; this time window (6 months plus 1-month grace period) was used in accordance with the coverage period of a denosumab injection, as stated in the clinical practice guidelines for osteoporosis in Bulgaria [16], and was in line with definitions of persistence that have been used in previous studies of denosumab [17, 18]. Women were not eligible if they were currently or had ever been enrolled in a clinical trial for denosumab, if they had participated in any clinical trial in the 6 months before their first denosumab injection, or if they were contraindicated for treatment with denosumab. All patients provided informed consent to allow access to their relevant medical records.

Study Sites and Data Collection

The study sites were selected on the basis of geographic area, availability of electronic or paper medical records, and the number of women with osteoporosis treated with denosumab. At each study site, the principal investigator reviewed the medical records of postmenopausal women initiating denosumab for osteoporosis in or after October 2011 who had received a second injection within 7 months of their first injection and before the end of the study period (August 2013). Up to a maximum number of eligible women per site (which was proportional to the number of women who met the inclusion criteria at each site and was specified in the study contract) were randomly selected for inclusion via a computerized system. Women enrolled into the study were followed up from the date of their first denosumab injection until the end of the study period, and the data required as per the study protocol were then transcribed onto an electronic case report form.

Study Outcomes

Data for all study variables were collected from the medical records made by physicians when patients visited the clinic to receive their denosumab injections. The variables included physician-related, socio-demographic, condition-related (including laboratory tests performed as part of routine clinical practice), and health-related characteristics. In addition, information was collected regarding denosumab prescription and administration, procedures pertaining to denosumab administration and osteoporosis, concomitant medication use, adverse events (AEs), and adverse drug reactions (ADRs) or serious ADRs.

BMD Measurement

Data on BMD at baseline and at 1 year after denosumab initiation (as required for local reimbursement) were collected for one or more of the following skeletal sites: lumbar spine (LS) in the posterior–anterior position; total hip (TH); and FN. To allow the mean change in a BMD T-score between baseline and 1 year to be calculated, both measurements had to have been taken at the same skeletal site and using the same dual x-ray absorptiometry (DXA) instrument. Across the study sites, the following DXA machine models were used: Lunar Prodigy, Lunar DPX-IQ (manufactured by General Electric Healthcare, Massachusetts, USA), Hologic 1500, Hologic 2000 and Hologic C (manufactured by Hologic, Massachusetts, USA). Owing to the different instruments used across the study sites, BMD T-scores were used instead of absolute BMD values. T-scores are presented as mean (SD) unless otherwise specified.

Statistical Analyses

The sample size of 200 women represents approximately 1% of the women with PMO in Bulgaria. Furthermore, based on the assumption that a prevalence of 1% or more of the population would have each of the patient-related characteristics, the chances of observing at least one event among a sample of 200 patients is 87%. Paired t tests were used to compare BMD T-scores recorded at baseline with those recorded after 1 year of treatment with denosumab. The χ ² test of independence was used to verify distributional independence of outcome variables and patient groupings. A significance level of 0.05 was used.

The outcome variables LS, TH, and FN BMD T-scores were analyzed according to the following patient categories: with/without previous fracture, exposed/not exposed to prior PMO therapy, and age group. Age and prior PMO therapy were analyzed according to whether patients had a previous fracture or not. Continuous variables were summarized using mean and SD or 95% confidence intervals (CIs); categorical values were summarized as the number and proportion of women in each category.

Results

Patient Characteristics at Baseline

A total of 228 women who met the eligibility criteria were randomly selected for this chart review from 13 sites in Bulgaria. Overall, 222 women were included in the analyses and their baseline characteristics are presented in Table 1. Of the six women excluded from the final analyses, three had exceeded the recommended interval between denosumab injections and three were excluded at the request of their physician. The mean (SD) age at initiation of denosumab was 64.2 (8.5) years. Half of all women were younger than 65 years, and 13.1% were aged 75 years or older. Approximately one-third (30.2%) of women had comorbidities at baseline.

Table 1.

Characteristics of Bulgarian women with PMO at denosumab initiation

Characteristic	Study population (n = 222)
Age at menopause, years, mean (SD)a	48.1 (4.0)
Time since PMO diagnosis, years, mean (SD)	1.8 (4.6)
Body mass index, n (%)
≤25 kg/m2	122 (55.0)
>25 kg/m2	77 (34.7)
No data	23 (10.4)
Current smoker, n (%)
Yes	24 (10.8)
No	192 (86.5)
Secondary osteoporosis, n (%)
Yes	6 (2.7)
No	216 (97.3)
Age at denosumab initiation, years, mean (SD)	64.2 (8.5)
Age at denosumab initiation, n (%)
<65 years	110 (49.5)
65–74 years	83 (37.4)
≥75 years	29 (13.1)
Comorbidities, n (%)b	67 (30.2)
Cardiovascular disease	37 (16.7)
Metabolic disorders	15 (6.8)
Gastrointestinal disorders	13 (5.9)
Osteoarthritis	6 (2.7)
Respiratory disorders	4 (1.8)
Central nervous system disorders	3 (1.4)
Rheumatoid arthritis	3 (1.4)
Height loss since maximal height, n (%)
Yes	110 (49.5)
No	112 (50.5)
Height loss, cm, mean (SD)	3.2 (1.9)
Family history of osteoporotic fracture, n (%)
Yes	43 (19.4)
No	179 (80.6)
Prior PMO therapy, n (%)
Yes	70 (31.5)
No	152 (68.5)
Calcium and/or vitamin D supplementation, n (%)
Both	78 (35.1)
Calcium only	13 (5.9)
Vitamin D only	6 (2.7)
None	125 (56.3)
Previous fracture, n (%)
Yes	59 (26.6)
1 fracturec	52 (88.1)
2 fracturesc	7 (11.9)
Fracture sitec
Hip	4 (6.8)
Vertebral	42 (71.2)
Other	19 (32.2)
Previous hospitalization for osteoporotic fracturec
Hospitalization	9 (15.3)
Surgery	8 (13.6)

PMO postmenopausal osteoporosis, SD standard deviation

^aData not available for 20 patients (n = 202)

^bComorbidities that were present in ≥1% of patients overall are presented

^cPercentages calculated from number of patients who had experienced a previous fracture

Approximately one-third (31.5%) of women had received prior osteoporosis therapy at any time during their history. The majority (56.3%) of women were not receiving dietary supplementation with calcium or vitamin D at baseline (Table 1), and few women were receiving calcium-only (5.9%) vitamin D-only (2.7%) supplements.

More than one-quarter (26.6%) of women reported a previous fracture. Of those reporting a previous fracture, 11.9% of women reported two previous fractures. The most common fracture type was vertebral (71.2% of women), followed by hip (6.8%). Hospitalization as a result of an osteoporotic fracture was reported for 15.3% of women (Table 1).

Of those who reported a previous fracture, only half (29/59; 49.2%) had received previous osteoporosis therapy. A χ ² test of independence found a statistically significant relationship between age group and previous fracture (p < 0.0001). Previous fractures were more prevalent in older women: 62.1% of women aged 75 years or older had experienced a previous fracture compared with 10.0% of those who were younger than 65 years (Table 2).

Table 2.

Previous fracture by age group in Bulgarian women with postmenopausal osteoporosis treated with denosumab

Previous fracture	Age groupa
	<65 years (n = 110)	65–74 years (n = 83)	≥75 years (n = 29)
Yes (n = 59)	11 (10.0)	30 (36.1)	18 (62.1)
No (n = 163)	99 (90.0)	53 (63.9)	11 (37.9)

Data shown are number of patients (%). Percentages are calculated from the total number of patients in each age group

^a χ ² test of independence demonstrated a significant relationship between age group and previous fracture (χ ² = 38.1051; p < 0.0001)

The indications given for prescribing denosumab are listed in Table 3. Most women (98.6%) were prescribed denosumab because they had a BMD T-score of less than −2.5 SD. The next most common reasons for initiating denosumab were history of osteoporotic fracture (22.1%) and multiple risk factors for fracture (20.3%). Some women (5.0%) were prescribed denosumab because they were intolerant to other therapies. More than one reason could be given per patient.

Table 3.

Indications for prescribing denosumab for Bulgarian women with PMO

Indication	Study population (n = 222)
BMD T-score <−2.5 SD	219 (98.6)
History of osteoporotic fracture	49 (22.1)
Multiple risk factors for fracture	45 (20.3)
Intolerant to other PMO therapies	11 (5.0)
Patient preference for convenience and safety	2 (0.9)

Categories as reported to the Bulgarian National Health Insurance Fund; more than one reason could be provided per patient. Data are shown as n (%)

BMD bone mineral density, PMO postmenopausal osteoporosis, SD standard deviation

Changes in BMD T-Scores at 1 Year

At baseline, mean (SD) BMD T-scores were −3.2 SD (0.6 SD) at the LS, −2.3 SD (0.8 SD) at the TH, and −2.7 SD (0.7 SD) at the FN (Fig. 1). After 1 year of denosumab treatment, mean BMD T-scores had increased significantly to −2.7 SD (0.6 SD), −2.1 SD (0.9 SD), and −2.4 SD (0.7 SD) at the LS, TH, and FN, respectively (Fig. 1). Increases in BMD T-scores were calculated for the women who met the criteria of having baseline and 1-year measurements performed at the same skeletal site and using the same DXA unit. Mean (95% CI) increases in BMD T-score were 0.47 SD (0.42–0.53; n = 183) at the LS, 0.27 SD (0.18–0.35; n = 64) at the TH, and 0.33 SD (0.26–0.39; n = 121) at the FN (all p < 0.0001, Fig. 1).

Fig.1.

BMD T-scores at baseline and after 1 year of denosumab treatment in Bulgarian women with postmenopausal osteoporosis. Data are shown as mean ± SD. Numbers within bars indicate numbers of patients. Values below bars indicate mean change in BMD T-score (95% confidence interval). Changes in BMD were calculated only for the women who met the criteria of having baseline and 1-year measurements performed at the same skeletal site and using the same dual X-ray absorptiometry instrument (n = 183 for lumbar spine, n = 64 for total hip, and n = 121 for femoral neck). Paired t tests were used to compare BMD T-scores recorded at baseline with those recorded at 1-year follow-up. BMD bone mineral density, SD standard deviation

Safety

No new fractures or serious falls were recorded in the year following initiation of denosumab. Furthermore, no AEs, serious AEs, or ADRs related to the use of denosumab were identified from the review of the medical records.

Discussion

In this retrospective, real-world chart review of women with PMO in Bulgaria receiving at least two injections of denosumab, the drug was usually prescribed to those at high fracture risk. In the patients who were persistent with treatment at 1 year, denosumab was well tolerated and was effective in increasing BMD T-scores at several skeletal sites.

The baseline characteristics of the enrolled Bulgarian women, such as age and time since menopause, were generally similar to those of patient populations in other studies [10, 19, 20]. However, baseline BMD T-scores were lower, indicating that the women were at a high risk of fracture [4, 5, 21, 22]. The low T-scores could reflect the local reimbursement criterion for denosumab in Bulgaria, which stipulates that the cost for denosumab 60 mg SC Q6M is partially reimbursed for those with a BMD T-score of −2.5 SD or less at one or more skeletal site.

The mean changes in BMD T-scores observed in our study were consistent with response to treatment and are similar to those reported in other studies of women with PMO who received treatment with denosumab. The beneficial effect of denosumab on BMD was also observed in another study over longer follow-up periods, with sustained improvements in BMD at several skeletal sites: cumulative 8-year increases of 18.4% at the LS and 8.3% at the TH were reported [23].

It has been reported for the year 2010 that only 5% of the 240,000 women in Bulgaria eligible for treatment for PMO received it [6]. A similar care gap has been reported in other countries worldwide [24–28]. In our study, only half of the women who had experienced previous fractures, and were therefore at a high risk of subsequent fracture, had received any prior treatment for PMO. This care gap may reflect Bulgarian reimbursement requirements, whereby women with PMO need to have annual DXA scans to assess their BMD. However, the availability of DXA scanning facilities is limited; there are only 34 scanners in Bulgaria, which is equivalent to approximately five scanners per million people, and most scanners are situated in large cities, which makes access difficult for less mobile women [29]. Furthermore, the cost of PMO therapy used to be reimbursed only up to 25% and women were required to cover the remaining 75% [29]. Consequently, many women would not have had access to PMO therapy, including denosumab. In 2014, the reimbursement rate for denosumab was increased to 50% of the total cost, which may increase patient access to therapy.

The care gap is also evident in the low proportion of women in our study who were receiving calcium or vitamin D supplementation at baseline, despite local guidelines advocating the use of these agents [29]. Calcium and vitamin D supplements are cost-effective supplements to PMO therapy [30] that have been shown to reduce bone loss and the incidence of non-vertebral fractures [31]. The low level of use of these agents is of concern and may be due to patients’ fears regarding the development of kidney stones or cardiovascular disease [32].

Denosumab was well tolerated by the women in this chart review study. No AEs were reported during the 1-year follow-up period, although it should be noted that, owing to the retrospective nature of the study, we could not control for AEs not being recorded in patients’ medical records. However, long-term data from the FREEDOM extension study have shown that the incidence of AEs did not increase over a treatment period of up to 9 years and that the incidence of fractures remained low [33, 34]. Other studies on the long-term safety of denosumab are ongoing.

There are some limitations to our study. No comparator was used; therefore, the changes in BMD T-scores between baseline and following denosumab initiation should be interpreted with care. In addition, because different DXA instruments were used at each study site, the use of absolute BMD values would not have allowed accurate grouping of data, so these data were not collected. Also, the women had received at least a second injection of denosumab within 7 months of the first injection and hence were persistent with treatment at 1 year; consequently, the results may not be generalizable to the entire population receiving denosumab for PMO, because women may not be persistent with denosumab therapy in real-world practice. However, other studies have shown that rates of persistence appear to be fairly high in routine clinical practice [17, 35].

Despite the limitations, this study provides insight into the efficacy of denosumab in a persistent population of women with PMO in Bulgaria.

Conclusion

This is the first real-world chart review study of women with PMO receiving denosumab in Bulgaria. Among women receiving two denosumab injections, BMD T-scores increased significantly at several skeletal sites after 1 year. No new fractures or new safety signals were observed. Treatment with denosumab was effective in a broad population of persistent patients for 1 year. Long-term therapy with denosumab may help to reduce the incidence of fracture and the subsequent burden on women with PMO and on healthcare systems.

Compliance with Ethical Standards

Conflict of interest

Mihail Boyanov has received speaker fees from MSD, Novartis, Roche, Amgen, Merck, and Aventis; honoraria for advisory board meetings from Amgen and MSD; and clinical trial funding from Amgen, Wyeth (Pfizer), and NPS Pharma. Alexander Shinkov has received fees as a speaker and consultant from Amgen, MSD, Servier, AstraZeneca, Hoffman-La Roche, Berlin-Chemie, Merck Serono, Abbott, Eli Lilly, and Teva. Michele Intorcia and Reneta Petkova are employees and shareholders of Amgen. Emi Psachoulia was an employee and a shareholder of Amgen at the time the study was conducted and when the manuscript was being prepared.

Ethical approval

The study protocol was approved by a central regulatory agency ethics committee, in accordance with the ethical principles of the Declaration of Helsinki.