Real-World Safety and Effectiveness of Denosumab in Patients with Osteoporosis: A Prospective, Observational Study in South Korea.

BACKGRUOUND: The efficacy and safety of denosumab have been established in a phase 3, randomized, placebo-controlled trial in Korean postmenopausal women with osteoporosis. This postmarketing surveillance study was aimed to investigate the safety and effectiveness of denosumab in Korean real-world clinical practice.
METHODS: Patients with osteoporosis who had received denosumab per the Korean approved indications in the postmarketing setting between September 2014 and September 2019 were enrolled. The primary endpoint was the incidence of adverse events (AEs) and adverse drug reactions (ADRs). The secondary endpoint was the percent change from baseline in bone mineral density (BMD) of the lumbar spine, total hip, and femoral neck.
RESULTS: Of the 3,221 patients enrolled, 3,185 were included in the safety analysis set; 2,973 (93.3%) were female, and the mean± standard deviation (SD) age was 68.9±9.9 years. The mean±SD study period was 350.0±71.4 days. AEs, fatal AEs, and ADRs occurred in 19.3%, 0.8%, and 1.6%, respectively. The most frequent AEs, occurring in >0.5% of patients, were dizziness (0.7%), arthralgia (0.7%), back pain (0.6%), and myalgia (0.6%). Hypocalcemia occurred in 0.3% of patients. There were no cases of osteonecrosis of the jaw and atypical femoral fracture. Mean±SD percent change from baseline in BMD of the lumbar spine, total hip, and femoral neck was 7.3%±23.6%, 3.6%±31.4%, and 3.2%±10.7%, respectively.
CONCLUSION: The safety and effectiveness of denosumab in Korean patients with osteoporosis in this study were comparable with those in the Korean randomized controlled trial, with no new safety findings.

GRAPHICAL ABSTRACT

INTRODUCTION

Osteoporosis is a systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to enhanced bone fragility and susceptibility to fracture [1]. Risk factors for osteoporosis include women aged ≥65 years, men aged ≥75 years, low body mass index (<18.5 kg/m2), North America and Asia region, family history of hip fracture, history of falls, low calcium and vitamin D intake, smoking, alcohol consumption, androgen deprivation therapy (ADT), aromatase inhibitor therapy (AIT), and long-term use of glucocorticoids [2-4]. Data from a Korea National Health and Nutrition Examination Survey (KNHANES; 2008 to 2011) showed that 22.4% of Korean adults aged ≥50 years had osteoporosis and 47.9% had osteopenia [5]. Another KNHANES reported that the prevalence of osteoporosis in Korean women and men aged ≥50 years was 38.0% and 7.3%, respectively [6].

Denosumab, a fully human monoclonal antibody administered subcutaneously once every 6 months (Q6M), reduces bone resorption and increases bone mineral density (BMD) by selectively targeting the receptor activator of nuclear factor kappa B ligand (RANKL), which is crucial for osteoclast differentiation, activation, and survival [7]. In the international, randomized, placebo controlled Fracture Reduction Evaluation of Denosumab in Osteoporosis Every 6 Months (FREEDOM) trial, denosumab significantly reduced the risk of new radiographic vertebral fracture, nonvertebral fracture, and hip fracture versus placebo in postmenopausal women with osteoporosis after 3 years of treatment [8]. Denosumab was well tolerated; there were no significant differences in the incidence of adverse events (AEs), serious AEs (SAEs), or discontinuation of study treatment because of AEs between patients treated with denosumab and those treated with placebo [8]. In an open-label extension (OLE) study of the FREEDOM trial, patients treated with denosumab for 3 years in the randomized controlled trial (RCT) continued taking denosumab for an additional 7 years (long-term group; total exposure to denosumab, up to 10 years) and those treated with placebo in the RCT received denosumab for up to 7 years (crossover group) [9]. Compared with a 3-year treatment period in the RCT, long-term treatment with denosumab resulted in a continuous increase in BMD, low fracture incidence, and low rates of AEs [9].

In a phase 3 RCT in Korean postmenopausal women with osteoporosis, a significant improvement in the mean percent change from baseline in BMD of the lumbar spine at month 6 was observed in patients treated with denosumab compared with those treated with placebo, and the efficacy increased at month 12 (mean percent change in lumbar spine BMD from baseline to month 12: 5.6%; 95% confidence interval [CI], 4.6% to 6.6%]) [10]. The AE profile was similar to that observed in denosumab trials conducted in other ethnic populations [10].

Denosumab was first approved in Korea in September 2014 for the treatment of postmenopausal women with osteoporosis, increasing bone mass in men with osteoporosis, treatment of bone loss in men receiving ADT for nonmetastatic prostate cancer, and treatment of bone loss in women receiving adjuvant AIT for breast cancer. In April 2019, denosumab was approved for the treatment of glucocorticoid-induced osteoporosis [11]. Since October 2017, denosumab is reimbursed twice a year under the Korean insurance plan for patients who have a T-score <−2.5 and insurance benefits are allowed six times for 3 years for patients who have been diagnosed with osteoporotic fracture on radiographic examination [12]. The 2020 Endocrine Society Guidelines recommend denosumab as one of the initial treatment options for postmenopausal women with osteoporosis who are at a high risk of osteoporotic fractures [13].

This postmarketing drug surveillance (PMS) study was conducted as a requirement of the Ministry of Food and Drug Safety, Republic of Korea, for products for which a marketing authorization application was submitted before July 1, 2015, to investigate the safety and effectiveness of denosumab administered in Korean real world clinical practice to patients with osteoporosis.

METHODS

Study objectives

The primary objective was to evaluate the incidence rates of AEs, SAEs, and adverse drug reactions (ADRs) among patients receiving denosumab in a postmarketing setting. Secondary objectives were to determine the effectiveness of denosumab by examining the change from baseline in BMD of the lumbar spine, total hip, and femoral neck (if available) and to describe the characteristics (e.g., demographics, medical history) of patients receiving denosumab in the postmarketing setting.

Study design

This was a prospective, observational, single arm study conducted between September 2014 and September 2019 in patients being treated with denosumab at 36 centers across Korea. Patients were followed up from the time of administration of the first dose of denosumab until the end of the 12-month period, death, or being lost to follow-up (e.g., patients transferred to another clinic), whichever occurred first. Eligible patients received a single dose of denosumab 60 mg during their initial visit or on day 1 (which could be the same day as screening) and returned for follow-up visits at the discretion of the investigator based on their course of treatment. Since the recommended dose of denosumab is 60 mg Q6M, patients who continued treatment had up to two follow-up visits during the 12-month follow-up period. The protocol was approved by the Institutional Review Board at each study site (representatively, no. 2017-0516 of the Asan Medical Center Ethics Review Committee), and the study was conducted in accordance with the Ethical Principles for Medical Research Involving Human Subjects outlined in the Declaration of Helsinki. All enrolled patients provided informed consent to participate in the study.

Patients

Eligible patients included those who had received denosumab for the approved indications in the postmarketing setting in Korea, were willing to provide access to their previous and future medical information and had consented to participate in the study. Patients were excluded if they had hypocalcemia, were pregnant, or had known hypersensitivity to denosumab or any of its components.

Treatment

Denosumab is formulated as a subcutaneous injection and administered at a dose of 60 mg Q6M for bone loss indications, in accordance with the Korean prescribing information [14]. A single subcutaneous injection of denosumab 60 mg Q6M was administered in the upper arm, upper thigh, or abdomen. If a dose was missed, the injection was administered as soon as the patient was available. Daily intake of calcium 1,000 mg and vitamin D ≥400 IU was recommended to all patients.

Assessments

Reports of AEs (including their seriousness and causal link to denosumab) were collected throughout the study period and coded using the Medical Dictionary for Regulatory Activities (MedDRA) version 22.1 [15]. An AE was defined as any untoward medical occurrence in a patient administered denosumab irrespective of a causal relationship with denosumab. An ADR was defined as any untoward medical occurrence in a patient administered denosumab in which there was a causal relationship between the occurrence of the event and treatment with denosumab as judged by the investigators. An SAE was defined as any AE that was fatal, life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, caused a congenital anomaly or birth defect, or was a significant medical hazard. Events of vertebral compression fracture and vertebral fracture were pooled and reported as vertebral compression fracture. There were no independent adjudication committees for osteonecrosis of the jaw (ONJ) and atypical femoral fracture (AFF). Effectiveness of denosumab was assessed by measuring the percent change from baseline in BMD of the lumbar spine, total hip, and femoral neck at 12 months. BMD was measured using dual-energy X-ray absorptiometry (DXA), per the study site’s clinical standard of measurement.

Statistical analysis

The target sample size was ≥3,000 patients, which was considered large enough to rule out an AE incidence of >0.1% with 95% CI if no AE was observed and to detect the known severe side effects of denosumab in ≥1 patient. The safety analysis set included enrolled patients who received ≥1 dose of denosumab and were followed up for AEs and excluded patients who did not receive denosumab during the study period and/or those with off label use. The effectiveness analysis set included patients from the safety analysis set for whom effectiveness (BMD measured at baseline and at least one subsequent time point at the same site) was evaluated. Descriptive analysis summarized categorical values by number and percentage. Continuous outcomes were summarized by the number of nonmissing values and mean±standard deviation (SD). Missing BMD data were not imputed. To identify the factors associated with an increased risk of AEs, a stepwise multivariate analysis was performed, and results expressed as odds ratios (ORs) and 95% CIs. The effects of prior bisphosphonate (BP) use, renal impairment, and hepatic impairment on the percent change from baseline in BMD of the lumbar spine, total hip, and femoral neck were determined by univariate analysis.

RESULTS

Patient disposition

Overall, 3,221 patients were enrolled, of whom 3,185 were included in the safety analysis set (Fig. 1). Thirty-six enrolled patients were excluded from the safety analysis set for not receiving denosumab treatment (n=28) and for off-label use of denosumab (n=8). A total of 2,605 (80.9%) patients completed the study. An additional 1,687 patients were excluded from the effectiveness analysis set due to the nonavailability of baseline or postbaseline BMD data and 1,498 patients were assessed for effectiveness.

Fig. 1.

Patient disposition. AE, adverse event; BMD, bone mineral density. aFour of eight patients treated with off-label denosumab were identified after three injections and included among those who completed the study; however, these patients were excluded from the safety analysis set and effectiveness analysis set. The dosing interval of the four patients was not based on the locally approved dosage; two patients had a 10-month interval, one had a 3-month interval, and one received two injections on the same day.

Demographics and baseline clinical characteristics

Of the 3,185 Korean patients included in the safety analysis set, 2,973 (93.3%) were female, and the mean±SD age was 68.9±9.9 years (Table 1). In total, 1,413 of 3,116 (45.3%) patients had a history of fracture, with prevalent vertebral fracture being the most common (30.1%). Postmenopausal osteoporosis (91.9%) was the most common cause of osteoporosis, followed by male osteoporosis (6.6%), bone loss due to AIT (1.4%), and bone loss due to ADT (0.06%). A total of 35.4% had an osteoporosis duration of ≥1 to <5 years, and 73.4% had a history of prior or current use of osteoporosis medications. Among the 1,498 patients in the efficacy analysis set, anatomical location osteoporosis rates were as follows: 68.5% in lumbar spine; 23.0% in total hip. Mean±SD BMD T-scores for the lumbar spine, total hip, and femoral neck were −2.8±0.97, −1.9±0.90, and −2.4±0.87, respectively.

Table 1.

Demographics and Baseline Clinical Characteristics of Patients

Variable	Safety analysis set (n=3,185)
Sex
Female	2,973 (93.3)
Male	212 (6.7)
Age, yr	68.9±9.9
<65	1,120 (35.2)
65–74	1,010 (31.7)
≥75	1,055 (33.1)
BMI, kg/m2	22.5±3.3
History of fracture[a]	1,413 (45.3)
Prevalent vertebral fracture	939 (30.1)
Prevalent hip fracture	236 (7.6)
Prevalent other fracture	454 (14.6)
Diagnosis
Postmenopausal osteoporosis	2,926 (91.9)
Male osteoporosis	211 (6.6)
Bone loss due to AIT	46 (1.4)
Bone loss due to ADT[b]	2 (0.06)
Duration of osteoporosis, yr
<1	874 (27.4)
≥1 to <5	1,127 (35.4)
≥5 to <10	661 (20.8)
≥10	468 (14.7)
Unknown	55 (1.7)
History of medication use for osteoporosis[a]
Never used[c]	780 (25.0)
Prior use or current use	2,288 (73.4)
Unknown[d]	48 (1.5)
History of BP use[a]
Not used	1,277 (40.1)
Previously used	1,699 (53.3)
Currently in use	46 (1.4)
Unknown	94 (3.0)
BMD T-score[e]
Lumbar spine	−2.8±0.97
Total hip	−1.9±0.90
Femoral neck	−2.4±0.87

Values are expressed as number (%) or mean±standard deviation.

BMI, body mass index; AIT, aromatase inhibitor therapy; ADT, androgen deprivation therapy; BP, bisphosphonate; BMD, bone mineral density.

Included in patients for whom information on previous medication use was available (n=3,116);

One patient was incorrectly reported to be female;

Defined “never used” in the history of osteoporosis medication as answered “never use” of BP and other medication in the medical history;

Defined “unknown” as answered “unknown” of BP and other medication in the medical history;

BMD data were analyzed in patients in the effectiveness analysis set for whom baseline and postbaseline BMD data were available (lumbar spine, n=1,423; total hip, n=1,222; femoral neck, n=1,362).

Treatment exposure

Overall, 2,062 (64.7%) patients received three doses of denosumab, and the mean±SD study period was 350.0±71.4 days.

Safety

AEs

Overall, 1,057 AEs occurred in 613 (19.3%) patients (Table 2). Most (618 [58.5%]) AEs were mild, whereas 305 (28.9%) AEs were moderate, and 133 (12.6%) AEs were severe. Overall, 71.7% of AEs resolved, 22.4% were ongoing, 3.3% resolved with sequelae, 2.5% were fatal, and 0.1% were unknown. AEs occurring in 36 (1.1%) patients led to the discontinuation of denosumab. The most frequent AEs, occurring in >0.5% of patients, were dizziness (0.7%), arthralgia (0.7%), back pain (0.6%), and myalgia (0.6%). A total of 227 (7.1%) patients experienced SAEs, with the most common SAEs being infections and infestations (1.4%), neoplasms (0.6%), and cardiac disorders (0.5%). Twenty-six (0.8%) patients experienced fatal AEs.

Table 2.

Incidence of AEs and ADRs Due to Denosumab

Variable	Safety analysis set (n=3,185)
	No. of patients (%)	No. of events
AEs	613 (19.3)	1,057
AEs leading to the discontinuation of denosumab	36 (1.1)	40
SAEs	227 (7.1)	295
Infections and infestations[a]	44 (1.4)	49
Neoplasms[b]	18 (0.6)	19
Cardiac disorders	16 (0.5)	18
Fatal AEs[c]	26 (0.8)	26
Most frequent AEs (>0.5%)
Dizziness	22 (0.7)	25
Arthralgia	21 (0.7)	21
Back pain	20 (0.6)	21
Myalgia	19 (0.6)	19
Pneumonia	17 (0.5)	17
Headache	16 (0.5)	17
AEs of special interest
Fracture	40 (1.3)	42
Musculoskeletal pain	28 (0.9)	28
Hypersensitivity	20 (0.6)	20
Hypocalcemia	10 (0.3)	11
Hyperparathyroidism tertiary	1 (0.03)	1
Fracture nonunion (delayed healing)	1 (0.03)	1
ADRs	50 (1.6)	62
Most frequent ADRs
Myalgia	10 (0.3)	10
Pain[d]	9 (0.3)	9
Hypocalcemia	9 (0.3)	10
Serious ADRs	3 (0.09)	4
Pneumonia	2 (0.06)	2
Vertebral compression fracture	1 (0.03)	2

AE, adverse event; ADR, adverse drug reaction; SAE, serious adverse event.

Aspiration pneumonia was excluded;

All benign tumors were excluded (e.g., uterine leiomyoma, thymoma);

Other fatal AEs included sepsis in two patients and bacterial sepsis, pneumonia, septic shock, gastric cancer, Hodgkin’s disease, lung neoplasm malignant, metastatic gastric cancer, cardiac arrest, cardiac failure, Still’s disease, cerebral hemorrhage, chronic obstructive pulmonary disease, and thrombosis in one patient each;

Includes general pains and shoulder and knee pains.

ADRs were reported in 50 (1.6%) patients, with myalgia (0.3%), pain (0.3%), and hypocalcemia (0.3%) being the most commonly reported ADRs. Serious ADRs were reported in three (0.09%) patients, which included pneumonia in two (0.06%) patients and vertebral compression fracture in one (0.03%) patient; pneumonia was considered to be related by the investigators.

AEs of special interest

Hypocalcemia was reported in 10 (0.3%) patients. Although calcium blood test was not recommended to be performed regularly, it was performed and reported if the physicians determined that hypocalcemia has occurred. Of those, eight (0.3%) patients did not have renal impairment at baseline and two (0.06%) patients had chronic kidney disease stage 3. Seventeen (0.6%) patients had undergone tooth extraction within 30 days before the day 1 visit (first dosing), and 30 (1.1%) patients had received a dental implant within 3 months preceding the day 1 visit. Despite these risk factors, there were no suspected reports of ONJ. One patient had undergone tooth extraction and received a dental implant 2 months after receiving the first dose of denosumab and continued treatment up to the end of the study, i.e., received three doses of denosumab. There were no reported AEs of AFF. Overall, 49 SAEs of infections and infestations occurred in 44 (1.4%) patients, of which two events, occurring in two (0.06%) patients, were considered serious ADRs. Common SAEs of infections and infestations included pneumonia in 10 (0.3%) patients (of which two were serious ADRs in two [0.06%] patients), influenza in six (0.2%) patients, and urinary tract infection in four (0.1%) patients. Eleven events of vertebral compression fracture were reported in nine patients. Eight patients experienced vertebral compression fracture during denosumab treatment as an AE, while one patient without a history of fracture experienced a vertebral compression fracture >6 months after the administration of the last dose of denosumab; follow-up data for antiosteoporotic treatment were not captured for this patient. Vertebral compression fracture in one (0.03%) patient as considered to be a serious ADR.

Post hoc analysis

Stepwise logistic regression analysis revealed that the incidence of AEs was higher in patients aged ≥75 years versus those aged <65 years (OR, 1.4; 95% CI, 1.1 to 1.8; P=0.0020) and in those with versus without the presence of medical history (OR, 1.9; 95% CI, 1.3 to 2.9; P=0.0023).

Effectiveness

Change in BMD of the lumbar spine, total hip, and femoral neck

Mean±SD percent changes from baseline in BMD of the lumbar spine, total hip, and femoral neck were 7.3%±23.6%, 3.6%±31.4%, and 3.2%±10.7%, respectively (Fig. 2). On univariate analysis, the percent change from baseline in BMD at all measured sites did not differ between patients with and those without prior BP use (Table 3).

Fig. 2.

Percent change from baseline in bone mineral density (BMD). Values are expressed as mean±standard deviation. BMD data were analyzed for patients whose baseline and follow-up BMD were available.

Table 3.

Effect of Prior BP Use on Percent Change in BMD with Denosumab

Variable	Percent change in BMD, %			P value[a]
	No.	Mean±SD	LS mean±SE
Lumbar spine
Prior use of BP
Yes	842	6.9±18.6	7.0±0.8	0.55
No	581	7.9±29.4	7.7±1.0
Total hip
Prior use of BP
Yes	734	3.9±40.0	3.9±1.2	0.61
No	488	3.0±8.2	3.0±1.4
Femoral neck
Prior use of BP
Yes	814	3.5±10.4	3.4±0.4	0.36
No	548	2.8±11.3	2.9±0.4

BP, bisphosphonate; BMD, bone mineral density; SD, standard deviation; LS, least squares; SE, standard error.

P for univariate analysis.

DISCUSSION

Osteoporosis is a chronic condition necessitating long-term and, sometimes, lifelong treatment [16]. The fear of rare side effects and concerns about long-term effectiveness are two of the most important reasons for the undertreatment of patients with osteoporosis [17]. Furthermore, the stringent eligibility criteria followed by RCTs such as FREEDOM limit the availability of safety and efficacy data of antiosteoporotic treatments in diverse populations, necessitating real-world evidence post-drug approval that can provide salient insights among a broader population in a clinical setting. Hence, we present the results from this large, observational real-world study establishing the safety and effectiveness of denosumab in patients with osteoporosis in Korea.

Compared with the 6-month incidence of AEs and SAEs in the Korean RCT, the incidence of AEs was lower (19.3% vs. 55.0%) but that of SAEs was higher (7.1% vs. 3.0%) in this real world study [10]. One-year data from FREEDOM OLE revealed the incidence of all AEs, SAEs, and malignancies to be 188.5, 11.8, and 1.8 yearly exposure adjusted patient incidence of AEs per 100 patient-years for long-term denosumab-treated patients, respectively [9]. Overall, these results suggest that denosumab was well tolerated by Korean patients with osteoporosis. Dizziness, arthralgia, myalgia, and back pain were some of the most frequent AEs reported in this study. Cardiac disorders were reported as an SAE in 0.5% of patients in this study. The findings of a meta analysis of RCTs of denosumab in patients with osteoporosis or osteopenia found that cardiac disorders were unlikely to be a consequence of denosumab use [18]. The investigators of this study also considered the relationship between denosumab use and cardiac disorders to be unlikely. Hypocalcemia as an ADR was reported in 0.3% of Korean patients with osteoporosis in this study versus 3.9% in the Japanese PMS study [14]. In this study, hypocalcemia was observed in patients with normal kidney function at baseline. In case of symptomatic hypocalcemia, clinical AEs reported by one patient were vertigo and dizziness. After the development of hypocalcemia, one patient required hospital admission for intravenous calcium supplementation. Eight patients were managed with initiating or increasing calcium supplementation as outpatients. Two patients discontinued denosumab due to hypocalcemia. In a retrospective cohort study in which Korean women were treated with a subcutaneous injection of denosumab (60 mg Q6M), approximately 8.2% of patients developed hypocalcemia [19]. Furthermore, an adjusted multiple regression model indicated that patients with low baseline albumin corrected calcium level and estimated glomerular filtration rate (lower than stage 3b) were significantly associated with an increased likelihood of developing hypocalcemia following treatment with denosumab [19].

Denosumab discontinuation results in a complete and rapid reversal of its effects on BMD and bone turnover markers, predisposing denosumab-treated patients to an increased risk of fracture [20]. In patients previously treated with denosumab who discontinue treatment, there is a rebound in bone turnover with an increase in vertebral fractures to the level observed in untreated patients [21]. A post hoc analysis of FREEDOM and its 10-year OLE study revealed that among patients who received ≥2 injections of denosumab Q6M, the risk of multiple vertebral fractures following cessation of denosumab was higher compared with that in patients who stopped placebo [22]. In this study, vertebral compression fracture was reported as an AE in nine patients and as a serious ADR in one patient, with one patient developing a fracture >6 months after the administration of the last dose of denosumab. As this study observed patients only for 1 year, this vertebral fracture could not be confirmed to be related to the discontinuation of denosumab. The Health Insurance Committee of the Korean Endocrine Society proposes that in patients with low or moderate risk for fractures after denosumab therapy, BPs or selective estrogen receptor modulator or hormone therapy must be used for 1 to 2 years along with vitamin D and calcium [23]. Patients at high or very high risk for fractures should continue on denosumab or switch to another therapy [23].

A total of 73.4% of patients in this study were current or previous users of medications to manage osteoporosis, indicating that most patients were not treatment-naïve. Despite enrolling patients pretreated with antiosteoporotic medications in this study compared with the Korean RCT, the mean percent change from baseline in BMD was comparable with that observed at month 12 in the Korean RCT which enrolled only treatment-naïve patients (lumbar spine, 7.3% vs. 5.6%) [10]. This suggests that denosumab treatment in Korean patients with osteoporosis is effective in a real-world clinical setting.

The percent change from baseline in BMD of the lumbar spine, total hip, and femoral neck in this study was independent of BP use. However, no requirement of a wash out period for patients with previous BP use is one of the limitations. The long-term residual effect of BP is likely to prevent bone resorption and, hence, preclude a BMD decrease. On the other hand, BP use has a blunting effect on the BMD increases when patients are transitioned to other therapies such as denosumab.

One strength of this PMS study is that it is the largest real-world study in Korea published to date that demonstrated the safety and effectiveness of denosumab in patients with osteoporosis. The study enrolled patients with male osteoporosis and those who developed osteoporosis following ADT and AIT, thereby establishing the safety and effectiveness of denosumab in indications other than postmenopausal osteoporosis, which was investigated in an RCT. However, this study has some limitations. Since the primary endpoint of this study was safety, the investigators used their discretion to collect data on treatment effectiveness. Thus, the baseline and postbaseline BMD were not evaluated in all patients; therefore, many patients were excluded in the effectiveness analysis set. Patients with glucocorticoid-induced osteoporosis were not enrolled as denosumab was not approved for this indication in Korea at the time of this study and, therefore, could not be investigated. Furthermore, fracture data were captured as a safety endpoint; therefore, the association between increase in BMD and reduction in the risk of fractures could not be determined. In terms of effectiveness analysis, one of the limitations of this study is that different types of DXA scan equipment were used in each center. Lack of cross-calibration procedures for DXA scanners at different facilities reduced sensitivity to detect significant change when comparing BMD among different centers. It is also possible that patients with secondary osteoporosis were not excluded. There was also a lack of data on bone turnover markers. Future studies should be focused on addressing these gaps as well as studying the effects of denosumab on treatment adherence and quality of life of patients with osteoporosis.

In conclusion, the safety and effectiveness of denosumab in Korean patients in this PMS study were similar to those in the Korean RCT and other real-world studies, with no new safety findings. Approximately 60.0% of AEs were mild, approximately 70.0% of AEs had resolved, and events of ONJ and AFF were not reported in this study. An improvement from baseline in BMD of the lumbar spine, total hip, and femoral neck was observed and was independent of prior BP use. Denosumab was well tolerated and showed a persistent increase in percent change in BMD in Korean patients with osteoporosis.