Nusinersen for Spinal Muscular Atrophy in the United States: Findings From a Retrospective Claims Database Analysis.

INTRODUCTION: Spinal muscular atrophy (SMA) is a rare, genetic neuromuscular disorder caused by deletion/mutation of the survival motor neuron 1 gene, characterized by progressive loss of motor neurons, resulting in increasing muscular weakness, deteriorating motor function, and, in its most severe form, death before 2 years. Nusinersen, an antisense oligonucleotide that increases expression of the functional SMN protein, was approved for SMA by US and European regulatory agencies in 2016 and 2017, respectively. The indicated regimen requires intrathecal injections every 4 months, following the first four injections during the loading phase. Adherence is integral to treatment success. Adherence to nusinersen may pose particular challenges as most patients with SMA are young children who require complex multidisciplinary care (including ongoing intrathecal treatment administration and potential specialized anesthetic and surgical procedures) at specialized centers. However, real-world data on adherence to nusinersen are limited.
METHODS: We conducted a retrospective claims database analysis from December 23, 2016, to November 20, 2019, to study nusinersen adherence and discontinuation/persistence in US patients with SMA types 1-3 who completed the loading phase, and to determine the impact of non-adherence or treatment discontinuation on SMA-related comorbidities, health care resource utilization (HCRU), and costs.
RESULTS: We identified 23 patients with SMA type 1, 41 patients with SMA type 2, and 260 patients with SMA type 3 who had completed the loading phase. Deviations from the indicated nusinersen treatment schedule were frequent in real-world usage, with most patients receiving ≥1 dose outside the scheduled interval. Across SMA types, non-adherent patients were more likely to have had SMA-related comorbidities (e.g., feeding difficulties, dyspnea and respiratory anomalies, and muscle weakness) and greater HCRU. Persistence rates 12 months after treatment initiation for patients with SMA types 1, 2, and 3 were 55.2%, 42.4%, and 54.6%, respectively. Patients who discontinued nusinersen and those who did not had generally similar comorbidity profiles. Discontinuation was associated with greater health care costs across SMA types.
CONCLUSION: Our analysis of claims data indicated that discontinuation and non-adherence to nusinersen treatment were prevalent, and associated with greater frequency of comorbidities, greater HCRU, and increased costs for patients.

Key Summary Points

Introduction

Spinal muscular atrophy (SMA) is a rare, genetic neuromuscular disorder caused by deletion or mutation of the survival motor neuron 1 (SMN1) gene [1]. SMA is characterized by wasting of alpha motor neurons in the spinal cord, resulting in increasing muscular weakness [1], and is the second most common fatal autosomal recessive disorder (cystic fibrosis being the most common) [1], with an estimated incidence of 1:11,000 live births [1, 2]. Without intervention, motor function deteriorates rapidly in patients with SMA type 1, typically resulting in death by 2 years of age [1].

The SMN2 gene is a back-up gene for SMN1, producing approximately 10% of the SMN protein obtained with one copy of SMN1 [3]. Therefore, SMN2 copy number is predictive of disease severity [4]. For example, the majority of patients with two copies of SMN2 have SMA type 1, the most severe form of the disease, with onset by 6 months of age and characterized by the inability to achieve independent sitting. Those patients with three SMN2 copies largely have SMA type 2, a less severe form of the disease, characterized by the inability to walk independently. The majority of patients with four copies of SMN2 have SMA type 3, in which patients walk independently.

Nusinersen, an antisense oligonucleotide, modifies splicing of the SMN2 gene such that functional SMN protein output is increased [5]. Nusinersen was approved for the treatment of SMA by the US Food and Drug Administration (FDA) in 2016 and by the European Medicines Agency in 2017 [6-8].

The indicated dosing regimen of nusinersen requires lifelong intrathecal injections every 4 months following the first four injections, administered during the loading phase [9]. Intrathecal administration presents challenges for patients with SMA, for example, the logistics of needing to travel to a clinic or the impact of repeated anesthesia/sedation exposure, particularly in infants and young children [10]. Moreover, the complex regimen nusinersen requires may be problematic for pediatric patients. In general, adherence to treatment for pediatric populations poses challenges [11, 12]. For example, adherence is dependent not only on the patient but also on the family [11]. Adherence and discontinuation are frequent issues associated with long-term treatment [11], and intrathecal administration poses additional challenges for adherence. By one estimate, approximately 50% of patients adhere to medication regimens [11].

Adherence is influenced by several factors, including adverse effects, cost of medication, dosing frequency, and routes of administration [11, 13], patient beliefs about medication(s), patient demographics, and comorbidities [14, 15]. Management guidelines, in general, do not specifically address patient adherence [16]. The importance of adherence was emphasized in the results of a recent systematic review of 190 randomized controlled trials, revealing a positive correlation between outcomes and patient compliance [17].

Several studies have indicated that patient non-adherence increases health care costs [11, 18, 19]. Non-adherence leads to poorer outcomes, which results in increased ancillary health care utilization and expenditures, and also creates a significant burden for health care systems [18, 19].

Because little real-world data exist for adherence to nusinersen treatment, we examined dosing patterns for patients with SMA types 1, 2, or 3 treated with nusinersen in the United States to estimate the extent to which patients adhered to the prescribed treatment schedule, and to describe the characteristics and outcomes of patients who adhered and those who were non-adherent to the treatment schedule. We also described characteristics and outcomes for patients who discontinued nusinersen therapy and for those who did not discontinue.

Methods

Data Source

We evaluated data from Symphony Health’s Integrated Dataverse® [20], a longitudinal patient data source that captures prescription claims and medical resource use and costs from across the US, and covers all payment types, including commercial insurance plans, Medicare Part D, Medicaid, and other assistance programs. The data from this source [20] link health care data from the US population from three primary sources (pharmacy point-of-service; switch/network transactions; direct prescriber, medical, and hospital claims data) and has data for 280 million active patients from 2003 through the present. We searched this database for patients diagnosed with SMA types 1, 2, and 3. Only patients who subsequently initiated nusinersen therapy after December 23, 2016 (US FDA approval date), were included in this study (Fig. 1).

Fig. 1

Sample selection. FDA US Food and Drug Administration, HCPCS Health Care Common Procedure Coding System, ICD-10-CM International Classification of Diseases, Tenth Revision, Clinical Modification, NDC National Drug Code, SMA spinal muscular atrophy. aThe observation period spanned from the first observed month of clinical activity until the last observed month of clinical activity or the end of data availability, whichever occurred first. bNusinersen treatment was identified based on either ≥1 claim for nusinersen injection or prescription fill, or ≥1 claim for unclassified drug or biologic injection on the same claim as an SMA diagnosis and for which the charged amount was between US $90,000 and $2,000,000, excluding claims with an NDC for onasemnogene abeparvovec.

This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors. The data that support the findings of this study are available from Symphony Health (https://symphonyhealth.prahs.com/), but restrictions apply to the availability of these data, which were used under license for the current study, and thus are not publicly available.

Patient Population and Study Design

This was a retrospective cohort study. Patients diagnosed with SMA were first identified, then SMA types were defined using: patient age at first observed diagnosis of SMA; age at end of recorded clinical activity or data availability; and symptoms, procedures, or use of a durable medical device [21]. Nusinersen treatment was identified using claims codes (one or more treatments with specific drug or treatment code). After nusinersen was approved, several months elapsed prior to the introduction of nusinersen-specific codes (NDC codes 64406-058-01 and 71860-396-01; specified HCPCS codes C9489 and J2326). Additional codes were used to identify patients who received nusinersen after FDA approval (required per protocol), using codes for unspecified biologics on medical claims with billing costs in the expected range for nusinersen (J2326; unspecified HCPCS codes C9399, J3490, and J359). Only patients who completed the loading dose regimen described below were included. Patients with ≥120 days between their first and second dosages were excluded.

The study design, including the loading phase study period, is described in Fig. 2. As per the approved label, patients were expected to have received four doses over the loading phase, followed by maintenance doses every 4 months [9]. Patients were followed from nusinersen initiation until last observed clinical activity or end of data availability (November 20, 2019). Given that onasemnogene abeparvovec gene therapy [22] was approved for the treatment of SMA during the time of the study (May 2019) [23], patients who also received onasemnogene abeparvovec gene replacement therapy were censored as of their treatment date. Risdiplam, an oral drug for the treatment of SMA, was not yet approved at the time of this study (approved August 2020) [24].

Fig. 2

Study design. SMA spinal muscular atrophy. aThe initiation of nusinersen was identified based on the first indicator for treatment with nusinersen

Outcomes and Statistical Analyses

Study outcomes measured included patient characteristics, adherence to nusinersen treatment schedule, comorbidities, treatment discontinuation and persistence, health care resource utilization (HCRU), and health care costs. Adherence rates were calculated as the percentage of doses received on time among all doses received. Treatment discontinuation was defined as two or more consecutive missed doses based on the expected dosing schedule per product label. The date of discontinuation was set to the date of the first missed dose. Treatment persistence for patients with SMA types 1, 2, and 3 was determined using the Kaplan–Meier estimator.

Health care resource utilization included outpatient visits (office and clinic), inpatient admissions, and other medical encounters, such as for home health, laboratory, or imaging work. HCRU was reported as incident rates per patient per year (PPPY), and calculated as the number of events divided by patient-years of observation. Incidence rates were calculated as number of events (e.g., outpatient visits) divided by patient-years of observation.

Total health care costs included medical service costs and pharmacy costs; they excluded those related to nusinersen and onasemnogene abeparvovec. Medical service costs were reported as amounts charged for procedures. Pharmacy costs were reported as final paid amounts. For inpatient stays, facility costs were derived using hospital-adjusted expenses/inpatient day for each US state [25]. In addition, costs for SMA-related procedures (excluding those for inpatient stays) were reported.

Patients who received all their nusinersen doses on time were defined as adherent to the dosing schedule, allowing for a grace period of ±7 days for loading doses and ±14 days for maintenance doses. Those who received one or more doses not on time were defined as non-adherent to the dosing schedule [26].

Patient characteristics related to discontinuation of treatment were evaluated. Outcomes were descriptively reported for each cohort. No statistical comparisons were conducted. Only numerical comparisons are presented in the context of this study.

Results

Demographics and Baseline Clinical Characteristics

Patient characteristics, demographics, and comorbidities are summarized in Table 1. We identified 62 patients with SMA type 1, 94 patients with SMA type 2, and 462 patients with SMA type 3 (Fig. 1). Patients who completed all four loading doses by SMA type were: 23 patients (37.1%) with SMA type 1, 41 (43.6%) with SMA type 2, and 260 (56.3%) with SMA type 3. Eligible patients with SMA types 1, 2, or 3 were selected as presented in Fig. 1.

Table 1

Patient characteristics, demographics, and comorbidities

	SMA type 1		SMA type 2		SMA type 3
	Discontinuation cohort (n = 11)	No discontinuation cohort (n = 12)	Discontinuation cohort (n = 24)	No discontinuation cohort (n = 17)	Discontinuation cohort (n = 146)	No discontinuation cohort (n = 114)
Duration of follow-upa (months), mean ± SD [median]	9.99 ± 8.43 [6.30]	15.51 ± 8.33 [15.37]	9.84 ± 8.20 [5.62]	17.88 ± 11.20 [18.97]	13.90 ± 10.65 [13.80]	16.76 ± 8.17 [17.65]
Demographic characteristics at the index date
Age (years), mean ± SD [median]	0.82 ± 0.75 [1.00]	0.67 ± 0.49 [1.00]	2.92 ± 1.61 [3.00]	2.76 ± 1.03 [3.00]	12.49 ± 8.53 [10.00]	17.53 ± 11.44 [14.50]
0–1, n (%)	9 (81.8)	12 (100.0)	2 (8.3)	1 (5.9)	0 (0.0)	0 (0.0)
2–3, n (%)	2 (18.2)	0 (0.0)	18 (75.0)	12 (70.6)	5 (3.4)	3 (2.6)
4–13, n (%)	0 (0.0)	0 (0.0)	4 (16.7)	4 (23.5)	88 (60.3)	51 (44.7)
14–20, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	38 (26.0)	25 (21.9)
21–34, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	12 (8.2)	24 (21.1)
35–49, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	2 (1.4)	11 (9.6)
50–65 +, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	1 (0.7)	0 (0.0)
Sex, n (%)
Female	7 (63.6)	7 (58.3)	9 (37.5)	9 (52.9)	68 (46.6)	69 (60.5)
Male	4 (36.4)	5 (41.7)	15 (62.5)	8 (47.1)	78 (53.4)	45 (39.5)
Type of health care plan at the index date, n (%)
Commercial	9 (81.8)	11 (91.7)	23 (95.8)	16 (94.1)	128 (87.7)	98 (86.0)
Medicaid/Medicare	0 (0.0)	1 (8.3)	1 (4.2)	1 (5.9)	8 (5.5)	15 (13.1)
Other/Unknown	2 (18.2)	0 (0.0)	0 (0.0)	0 (0.0)	10 (6.8)	1 (0.9)
Comorbidity profilea, b
SMA-related comorbidities, n (%)
Feeding difficulties and mismanagement	5 (45.5)	5 (41.7)	6 (25.0)	4 (23.5)	24 (16.4)	8 (7.0)
Dyspnea and respiratory anomalies	4 (36.4)	5 (41.7)	6 (25.0)	4 (23.5)	32 (21.9)	42 (36.8)
Dysphagia, unspecified	4 (36.4)	6 (50.0)	5 (20.8)	1 (5.9)	25 (17.1)	19 (16.7)
Failure to thrive	3 (27.3)	5 (41.7)	7 (29.2)	3 (17.6)	11 (7.5)	7 (6.1)
Constipation	3 (27.3)	6 (50.0)	6 (25.0)	6 (35.3)	31 (21.2)	24 (21.1)
Acute respiratory failure	2 (18.2)	2 (16.7)	5 (20.8)	5 (29.4)	17 (11.6)	18 (15.8)
Scoliosis	1 (9.1)	4 (33.3)	5 (20.8)	5 (29.4)	72 (49.3)	66 (57.9)
Chronic respiratory failure	3 (27.3)	2 (16.7)	4 (16.7)	2 (11.8)	39 (26.7)	32 (28.1)
Muscle weakness (generalized)	2 (18.2)	3 (25.0)	10 (41.7)	8 (47.1)	48 (32.9)	36 (31.6)
Contractures	1 (9.1)	0 (0.0)	3 (12.5)	3 (17.6)	22 (15.1)	23 (20.2)
Mental comorbidities, n (%)b
Sleep–wake disorders	2 (18.2)	5 (41.7)	7 (29.2)	5 (29.4)	40 (27.4)	35 (30.7)
Other conditions that may be a focus of clinical attention	1 (1.9)	3 (25.0)	3 (12.5)	2 (11.8)	9 (6.2)	5 (4.4)
Anxiety disorders	0 (0.0)	0 (0.0)	1 (4.2)	2 (11.8)	9 (6.2)	20 (17.5)
Elimination disorders	0 (0.0)	0 (0.0)	3 (12.5)	1 (5.9)	30 (20.5)	21 (18.4)

SD standard deviation, SMA spinal muscular atrophy

aMeasured at any time point during the observation period, which spanned from nusinersen initiation until the last month of clinical activity, date of reinitiation after discontinuation, an indication of treatment with onasemnogene abeparvovec, or the end of data availability (November 30, 2019), whichever came first

bOnly comorbidities occurring in >5% of patients are presented. Other chronic comorbidities include chronic pulmonary disease and hemiplegia or paraplegia

Adherence

Mean (SD) nusinersen adherence rates across SMA types were similar: 71.8% (29.9%), 74.4% (22.8%), and 75.6% (25.8%) for SMA types 1, 2, and 3, respectively (Table 2). Allowing for a grace period of ±7 days for loading doses and ±14 days for maintenance doses, at least one dose was received off-schedule by 13 of 23 patients (56.5%) with SMA type 1, 30 of 41 patients (73.2%) with SMA type 2, and 158 of 260 patients (60.8%) with SMA type 3 (Table 2).

Table 2

Nusinersen dosage schedule adherencea,b

	SMA type 1 (n = 23)	SMA type 2 (n = 41)	SMA type 3 (n = 260)
Number of patients with at least one dose off-schedule, n (%)	13 (56.5)	30 (73.2)	158 (60.8)
Adherence rate, mean ± SD	71.84 ± 29.85	74.37 ± 22.82	75.57 ± 25.78
Minimum	16.7%	25.0%	20.0%
10th percentile	25.0%	40.0%	40.0%
25th percentile	46.2%	58.3%	55.6%
Median	83.3%	80.0%	83.3%
75th percentile	100.0%	100.0%	100.0%
90th percentile	100.0%	100.0%	100.0%
Maximum	100.0%	100.0%	100.0%

SD standard deviation, SMA spinal muscular atrophy

aAdherence rate was defined as the percentage of doses received on time out of all doses received. Patients who received all their nusinersen doses on time were defined as adherent to nusinersen dosage schedule, and those who received one or more doses not on time were defined as non-adherent to nusinersen dosage schedule

bDoses were considered not on time using grace periods of ±7 days for loading doses and ±14 days for maintenance doses. Patients with ≥120 days between their first and second dosage were considered as in the maintenance phase and were expected to follow the maintenance dosing schedule

Patients who did not adhere to treatment had greater SMA-related comorbidities across all SMA types, including feeding difficulties, dyspnea and respiratory anomalies, failure to thrive, and muscle weakness. Non-adherent patients also demonstrated more neurodevelopmental disorders, sleep–wake disorders, and chronic pulmonary disease compared with adherent patients (Table 3).

Table 3

Patient characteristics for adherent versus non-adherent patients

Patient characteristic	SMA type 1		SMA type 2		SMA type 3
	Adherent cohort (n = 11)	Non-adherent cohort (n = 12)	Adherent cohort (n = 12)	Non-adherent cohort (n = 29)	Adherent cohort (n = 122)	Non-adherent cohort (n = 138)
Duration of follow-upa (months), mean ± SD [median]	14.23 ± 8.37 [14.07]	21.01 ± 6.77 [21.05]	11.07 ± 9.27 [6.03]	21.08 ± 7.80 [24.23]	13.50 ± 7.60 [13.62]	19.49 ± 6.96 [19.13]
Demographic characteristics at the index date
Age (years), mean ± SD [median]	0.55 ± 0.52 [1.00]	0.92 ± 0.67 [1.00]	2.83 ± 1.03 [2.50]	2.86 ± 1.53 [3.00]	16.46 ± 10.96 [14.00]	13.14 ± 9.25 [10.00]
0–1, n (%)	11 (100.0)	10 (83.3)	0 (0.0)	3 (10.3)	0 (0.0)	0 (0.0)
2–3, n (%)	0 (0.0)	2 (16.7)	9 (75.0)	21 (72.4)	1 (0.8)	7 (5.1)
4–13, n (%))	0 (0.0)	0 (0.0)	3 (25.0)	5 (17.2)	58 (47.5)	81 (58.7)
14–20, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	34 (27.9)	29 (21.0)
21–34, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	20 (16.4)	16 (11.6)
35–49, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	8 (6.6)	5 (3.6)
50–65 +, n (%)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	1 (0.8)	0 (0.0)
Sex, n (%)
Female	8 (72.7)	6 (50.0)	6 (50.0)	12 (41.4)	62 (50.8)	75 (54.3)
Other/unknown	3 (27.3)	0 (0.0)	0 (0.0)	2 (6.9)	0 (0.0)	1 (0.7)
Type of health care plan at index date, n (%)
Commercial	10 (90.9)	10 (83.3)	12 (100.0)	27 (93.1)	104 (85.2)	122 (88.4)
Medicaid, Medicare	0 (0.0)	1 (8.3)	0 (0.0)	2 (6.9)	14 (11.5)	9 (6.5)
Other/unknown	1 (9.1)	1 (8.3)	0 (0.0)	0 (0.0)	4 (3.3)	7 (5.1)
Comorbidity profileb
SMA-related comorbidities, n (%)
Feeding difficulties and mismanagement	4 (36.4)	7 (58.3)	0 (0.0)	12 (41.4)	12 (9.8)	20 (14.5)
Dyspnea and respiratory anomalies	4 (36.4)	8 (66.7)	7 (58.3)	15 (51.7)	36 (29.5)	43 (31.2)
Dysphagia, unspecified	5 (45.5)	7 (58.3)	0 (0.0)	9 (31.0)	16 (13.1)	30 (21.7)
Failure to thrive	6 (54.5)	5 (41.7)	1 (8.3)	9 (31.0)	6 (4.9)	12 (8.7)
Constipation	6 (54.5)	3 (25.0)	4 (33.3)	11 (37.9)	28 (23.0)	35 (25.4)
Acute respiratory failure	2 (18.2)	5 (41.7)	1 (8.3)	11 (37.9)	13 (10.7)	27 (19.6)
Scoliosis	3 (27.3)	5 (41.7)	1 (8.3)	17 (58.6)	68 (55.7)	85 (61.6)
Chronic respiratory failure	1 (9.1)	5 (41.7)	0 (0.0)	9 (31.0)	31 (25.4)	39 (28.3)
Muscle weakness (generalized)	1 (9.1)	5 (41.7)	6 (50.0)	14 (48.3)	36 (29.5)	53 (38.4)
Contractures	0 (0.0)	1 (8.3)	1 (8.3)	7 (24.1)	18 (14.8)	32 (23.2)
Mental comorbidities, n (%)b
Neurodevelopmental disorders	3 (27.3)	3 (25.0)	4 (33.3)	10 (34.5)	13 (10.7)	29 (21.0)
Sleep–wake disorders	5 (45.5)	2 (16.7)	4 (33.3)	9 (31.0)	32 (26.2)	44 (31.9)
Other conditions that may be a focus of clinical attention	2 (18.2)	2 (16.7)	0 (0.0)	5 (17.2)	9 (7.4)	10 (7.2)
Anxiety disorders	0 (0.0)	0 (0.0)	0 (0.0)	5 (17.2)	21 (17.2)	24 (17.4)
Elimination disorders	0 (0.0)	1 (8.3)	0 (0.0)	5 (17.2)	21 (17.2)	32 (23.2)

SD standard deviation, SMA spinal muscular atrophy

aMeasured at any time point during the study period. The study period spanned from the index date until the last observed month of clinical activity, the date of nusinersen reinitiation after discontinuation, an indicator of treatment with onasemnogene abeparvovec, or the end of data availability (i.e., Nov. 30, 2019), whichever occurred first

bOnly comorbidities occurring in ≥5% of patients are presented. Other chronic comorbidities include chronic pulmonary disease and hemiplegia or paraplegia

Discontinuation and Persistence Analyses

Median time to nusinersen discontinuation was 18.5 months among patients with SMA type 1, with a persistence rate of 55.2% at 12 months post-initiation (Fig. 3). Analysis of treatment persistence revealed that <50% of patients, regardless of SMA type, remained on treatment 24 months after starting nusinersen (Fig. 3). The time to discontinuation among patients with SMA types 2 and 3 was 6.2 and 14.4 months, respectively, with persistence rates at 12 months of 42.4% and 54.6%, respectively. Mean ages (months ± SD) of patients who discontinued nusinersen were 0.82 ± 0.75, 2.92 ± 1.61, and 12.49 ± 8.53 for patients with SMA types 1, 2, and 3, respectively (Table 1). Mean ages (months ±SD) of patients who did not discontinue nusinersen were 0.67 ± 0.49, 2.76 ± 1.03, and 17.53 ± 11.44 for SMA types 1, 2, and 3, respectively (Table 1).

Fig. 3

Persistence to nusinersen for patients with SMA. KM Kaplan Meier, SMA spinal muscular atrophy. aPatients were observed from the index date until nusinersen discontinuation, an indicator of treatment with onasemnogene abeparvovec, or end of data availability (November 30, 2019), whichever occurred first. Treatment discontinuation was defined as two or more consecutive missed doses based on the expected dosing schedule per product label. The date of discontinuation was set to the date of the first missed dose. bPatients who were still observed at the specific time, that is, patients who did not discontinue before that time point and who are not censored at that point

SMA-Related Comorbidities

Comorbidity profiles for patients who discontinued compared with patients who did not discontinue were similar for each cohort. The most common comorbidities varied by SMA type. For patients with SMA type 1, the most common comorbidity was feeding difficulties [45.5% (n = 5/11) and 41.7% (n = 5/12) for discontinuation cohort and no discontinuation cohort, respectively; Table 1]. SMA type 2 patients presented with generalized muscle weakness as the most common comorbidity [41.7% (n = 10/24) and 47.1 (n = 8/17) for the discontinuation cohort and no discontinuation cohort, respectively; Table 1]. For patients with SMA type 3, the most common comorbidity reported was scoliosis [49.3% (n = 72/146) and 57.9% (n = 66/114) for the discontinuation cohort and no discontinuation cohort, respectively; Table 1).

Health Care Resource Utilization and Cost Analyses

Non-Adherent or Adherent Patients

Patients with SMA types 1, 2, and 3 who were non-adherent to nusinersen treatment had greater HCRU days PPPY compared with patients who were adherent to the dosing schedule. Overall HCRU days PPPY for non-adherent patients with SMA types 1, 2, and 3 were 48.4, 109.6, and 71.7, respectively. For adherent patients, HCRU days PPPY were 42.2, 45.2, and 54.8 for SMA types 1, 2, and 3, respectively (Supplemental Table 1).

While patients received treatment, health care costs [excluding nusinersen costs; mean ± SD (median)] reached $59,244 ± $80,492 ($28,915) PPPY for patients with SMA type 1 in the non-adherent cohort and $85,042 ± $122,187 ($21,448) PPPY for patients in the adherent cohort (Table 4). Non-adherent patients with SMA type 2 incurred $146,830 ± $172,157 ($84,428) PPPY compared with $51,937 ± $42,221 ($40,537) PPPY incurred by adherent patients (Table 4). For patients with SMA type 3, these costs were $105,657 ± $222,385 ($31,485) PPPY for the non-adherent cohort and $74,647 ± $138,899 ($30,968) PPPY for the adherent cohort (Table 4).

Table 4

Health care costs for patients adherent and non-adherent to nusinersen dose schedule

Health care costs per patient per year (2020 USD)a	SMA type 1		SMA type 2		SMA type 3
	Adherent cohort	Non-adherent cohort	Adherent cohort	Non-adherent cohort	Adherent cohort	Non-adherent cohort
	n = 11	n = 12	n = 12	n = 29	n = 122	n = 138
Total health care costs (excluding costs related to nusinersen and onasemnogene abeparvovec), mean ± SD [median]	85,042 ± 122,187 [21,448]	59,244 ± 80,492 [28,915]	51,937 ± 42,221 [40,537]	146,830 ± 172,157 [84,428]	74,647 ± 138,899 [30,968]	105,657 ± 222,385 [31,485]
Q1–Q3	10,766–106,502	18,386–59,264	20,528–71,725	29,962–175,393	10,948–73,797	9832–82,727
Minimum–maximum	8911–410,939	1099–290,785	4442–133,784	0–567,580	0–896,196	0–1,499,117
Medical service costs	79,044 ± 114,186 [20,503]	58,382 ± 80,610 [27,713]	51,886 ± 42,227 [40,523]	145,790 ± 170,434 [84,426]	71,859 ± 136,953 [28,622]	103,581 ± 221,910 [29,160]
Inpatientb	35,567 ± 107,821 [0]	10,436 ± 15,776 [2,630]	3754 ± 6126 [0]	29,104 ± 59,503 [2390]	9089 ± 44,374 [0]	9618 ± 28,972 [0]
Outpatient (including office and clinic)	18,764 ± 15,359 [20,092]	19,324 ± 14,944 [15,657]	37,835 ± 35,690 [33,610]	34,428 ± 30,848 [25,378]	19,913 ± 20,640 [12,652]	22,326 ± 30,492 [14,403]
Other	24,713 ± 44,028 [5933]	28,622 ± 62,128 [4413]	10,298 ± 17,499 [3438]	82,259 ± 140,120 [18,859]	42,857 ± 115,255 [3308]	71,636 ± 191,743 [3342]
Pharmacy costs	5998 ± 14,635 [0]	863 ± 1569 [131]	50 ± 64 [31]	1039 ± 3218 [40]	2789 ± 10,552 [176]	2076 ± 5509 [190]
SMA-related costs (excluding facility costs for inpatient stays), mean ± SD [median]	11,824 ± 17,034 [1835]	16,136 ± 33,424 [5970]	11,720 ± 12,800 [8581]	24,948 ± 33,409 [11,571]	19,238 ± 65,662 [2323]	26,277 ± 127,681 [1967]
Mechanical ventilation	158 ± 285 [0]	418 ± 1321 [0]	0 ± 0 [0]	640 ± 1196 [0]	3892 ± 28,222 [0]	611 ± 1713 [0]
Non-invasive	158 ± 285 [0]	418 ± 1321 [0]	0 ± 0 [0]	602 ± 1200 [0]	3627 ± 27,866 [0]	574 ± 1683 [0]
Invasive	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	38 ± 132 [0]	265 ± 2198 [0]	37 ± 249 [0]
Tracheostomy	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	10 ± 116 [0]	13 ± 108 [0]
Nutritional support	14,931 ± 30,572 [1,835]	12,330 ± 29,536 [2147]	0 ± 0 [0]	18,081 ± 32,418 [0]	13,198 ± 54,166 [0]	23,833 ± 125,447 [0]
Gastrostomy	5765 ± 13,745 [0]	11,977 ± 29,023 [1942]	0 ± 0 [0]	14,031 ± 27,960 [0]	11,546 ± 52,222 [0]	21,980 ± 124,215 [0]
Nasogastric tube or other (non-oral feeding support)	9166 ± 29,350 [0]	344 ± 626 [0]	0 ± 0 [0]	4041 ± 15,474 [0]	1631 ± 8786 [0]	1842 ± 6393 [0]
Nutritional counseling	0 ± 0 [0]	9 ± 30 [0]	0 ± 0 [0]	9 ± 50 [0]	21 ± 85 [0]	11 ± 57 [0]
Physical and/or occupational therapy/rehabilitation	5902 ± 12,777 [0]	3742 ± 6676 [157]	11,171 ± 12,455 [8,581]	9451 ± 15,114 [3,786]	3504 ± 7386 [136]	3289 ± 7738 [0]
Speech therapy	5 ± 16 [0]	301 ± 845 [5]	0 ± 0 [0]	1210 ± 2167 [0]	262 ± 1196 [0]	350 ± 2213 [0]
Sleep studies	2960 ± 4763 [0]	231 ± 802 [0]	1928 ± 4379 [0]	1360 ± 2560 [0]	543 ± 1980 [0]	491 ± 1400 [0]
Orthopedic surgery	0 ± 0 [0]	62 ± 216 [0]	298 ± 1034 [0]	370 ± 1174 [0]	941 ± 7675 [0]	1056 ± 3893 [0]
Chiropractic services	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	1 ± 7 [0]
Osteopathic services or acupuncture	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]
SMA-related DME (excluding facility costs for inpatient stays), n (%)	0 ± 0 [0]	0 ± 0 [0]	2398 ± 5125 [0]	1338 ± 1188 [1088]	356 ± 1063 [0]	427 ± 1211 [0]
Braces	0 ± 0 [0]	0 ± 0 [0]	550 ± 1083 [0]	826 ± 900 [716]	285 ± 948 [0]	384 ± 1159 [0]
Pediatric wheelchair (tilt-in-space)	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	444 ± 1083 [0]	0 ± 0 [0]	0 ± 0 [0]
Pediatric wheelchair	0 ± 0 [0]	0 ± 0 [0]	1848 ± 4401 [0]	68 ± 258 [0]	70 ± 452 [0]	0 ± 0 [0]
Manual adult wheelchair	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	43 ± 355 [0]
Walker or cane	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]

DME durable medical equipment, SD standard deviation, SMA spinal muscular atrophy, US United States

aCosts for procedures recorded on the same claim as an indicator of treatment with nusinersen or onasemnogene abeparvovec were excluded. Costs were assessed while on treatment, that is from the first observed nusinersen dose (i.e., index date) until (1) the last dose date + expected inter-dose interval based on product label (i.e., date of next expected dose), (2) an indicator of treatment with onasemnogene abeparvovec, or (3) the end of data availability (i.e., November 30, 2019), whichever occurred first

bInpatient costs included costs of medical procedures received in an inpatient setting and facility costs. Facility costs were imputed using hospital adjusted expenses per inpatient day for each US state reported by the Henry J. Kaiser Family Foundation; the facility costs (from the institutional perspective; i.e., charged amounts) were imputed based on patient’s respective US state and the length of inpatient stay (https://www.kff.org/health-costs/state-indicator/expenses-per-inpatient-day)

Patients Who Discontinued or Did Not Discontinue

On average, patients with SMA type 1 who discontinued nusinersen (n = 11) had 326 events with medical services, while those who did not discontinue nusinersen (n = 12) had 805 events with medical services. However, patients with SMA types 2 and 3 who discontinued nusinersen had, on average, more events with medical services than those who did not discontinue (1971 events compared with 1888 events, respectively, for patients with SMA type 2; 9883 events compared with 9078 events, respectively, for patients with SMA type 3). Findings varied among the subgroup of patients who received their four loading doses because of a small sample size (Supplemental Table 2).

Over the observation period, patients with SMA type 1 who discontinued nusinersen had, on average, greater total health care costs (excluding nusinersen costs) than those who did not discontinue [mean ± SD (median): $92,678 ± $164,502 ($19,782) compared with $79,352 ± $114,717 ($30,262) PPPY, respectively]. Similarly, for SMA types 2 and 3, patients who discontinued nusinersen incurred greater average total health care costs PPPY than those who did not discontinue: SMA type 2: $110,468 ± $134,239 ($71,674) compared with $92,566 ± $136,496 ($40,184); SMA type 3: $96,787 ± $196,245 ($24,434) compared with $82,253 ± $188,851 ($35,752) (Table 5).

Table 5

Health care costs for patients who discontinued and did not discontinue nusinersen

Health care costs per patient per year (2020 USD)a	SMA type 1		SMA type 2		SMA type 3
	Discontinued (n = 11)	Not discontinued (n = 12)	Discontinued (n = 24)	Not discontinued (n = 17)	Discontinued (n = 146)	Not discontinued (n = 114)
Total health care costs (excluding costs related to nusinersen and onasemnogene abeparvovec), mean ± SD [median]	92,678 ± 164,502 [19,782]	79,352 ± 114,717 [30,262]	110,468 ± 134,239 [71,674]	92,566 ± 136,496 [40,184]	96,787 ± 196,245 [24,434]	82,253 ± 188,851 [35,752]
Q1–Q3	12,151–89,770	11,682–103,412	19,596–127,590	29,254–88,198	8561–91,823	10,948–76,785
Minimum–Maximum	457–558,556	8911–410,939	0–486,456	0–567,580	0–1,299,960	0–1,499,117
Medical service costs	89,493 ± 162,849 [19,782]	77,181 ± 109,981 [29,790]	109,456 ± 132,506 [71,290]	92,362 ± 135,910 [40,184]	94,944 ± 195,152 [23,774]	79,192 ± 188,005 [32,298]
Inpatientb	20,972 ± 54,369 [0]	36,432 ± 102,850 [0]	14,430 ± 37,721 [0]	21,705 ± 35,147 [2261]	9161 ± 32,489 [0]	9638 ± 44,536 [0]
Outpatient (including office and clinic)	24,157 ± 30,422 [11,356]	27,038 ± 21,727 [21,395]	33,605 ± 31,421 [27,654]	31,843 ± 26,401 [30,971]	20,803 ± 27,482 [10,508]	21,960 ± 26,008 [13,873]
Other	44,364 ± 94,069 [530]	13,711 ± 19,036 [5402]	61,421 ± 113,458 [16,875]	38,815 ± 97,713 [4805]	64,979 ± 171,600 [3853]	47,594 ± 158,812 [2791]
Pharmacy costs	3186 ± 9610 [223]	2171 ± 5074 [0]	1011 ± 2687 [57]	204 ± 657 [22]	1843 ± 6492 [149]	3061 ± 9862 [177]
SMA-related costs (excluding facility costs for inpatient stays), mean ± SD [median]	6155 ± 9516 [323]	13,593 ± 16,524 [5564]	19,489 ± 26,912 [9118]	11,850 ± 12,102 [9229]	15,192 ± 37,155 [1365]	25,955 ± 136,766 [1711]
Mechanical ventilation	1690 ± 5306 [0]	114 ± 268 [0]	872 ± 1766 [0]	386 ± 1264 [0]	1013 ± 2843 [0]	3408 ± 29,016 [0]
Non-invasive	1690 ± 5306 [0]	114 ± 268 [0]	691 ± 1612 [0]	359 ± 1255 [0]	1001 ± 2830 [0]	3123 ± 28,646 [0]
Invasive	0 ± 0 [0]	0 ± 0 [0]	181 ± 884 [0]	27 ± 81 [0]	11 ± 76 [0]	285 ± 2261 [0]
Tracheostomy	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	4 ± 44 [0]	15 ± 119 [0]
Nutritional support	13,474 ± 32,054 [0]	5751 ± 13,118 [0]	12,713 ± 26,177 [0]	2396 ± 5877 [0]	12,839 ± 39,142 [0]	20,214 ± 130,110 [0]
Gastrostomy	3433 ± 5978 [0]	5498 ± 13,188 [0]	10,893 ± 24,389 [0]	2377 ± 5856 [0]	10,738 ± 34,867 [0]	19,085 ± 129,147 [0]
Nasogastric tube or other (non-oral feeding support)	10,027 ± 32,642 [0]	252 ± 699 [0]	1820 ± 3147 [0]	3 ± 11 [0]	2093 ± 9,816 [0]	1117 ± 4157 [0]
Nutritional counseling	14 ± 46 [0]	0 ± 0 [0]	0 ± 0 [0]	16 ± 66 [0]	9 ± 46 [0]	12 ± 60 [0]
Physical and/or occupational therapy/rehabilitation	1031 ± 3314 [0]	7981 ± 12,675 [1540]	6961 ± 11,540 [667]	8644 ± 11,408 [5427]	2893 ± 6875 [0]	3127 ± 7512 [0]
Speech therapy	603 ± 1389 [0]	5 ± 15 [0]	1017 ± 2164 [0]	196 ± 807 [0]	239 ± 2100 [0]	365 ± 1722 [0]
Sleep studies	331 ± 1099 [0]	2560 ± 4575 [0]	1634 ± 5791 [0]	1157 ± 2560 [0]	312 ± 1685 [0]	498 ± 1597 [0]
Orthopedic surgery	0 ± 0 [0]	0 ± 0 [0]	152 ± 564 [0]	299 ± 1234 [0]	1193 ± 6354 [0]	621 ± 3393 [0]
Chiropractic services	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	1 ± 7 [0]
Osteopathic services, acupuncture	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]
SMA-related DME (excluding facility costs for inpatient stays), n (%)	0 ± 0 [0]	0 ± 0 [0]	939 ± 1842 [0]	983 ± 1589 [0]	545 ± 4060 [0]	388 ± 1084 [0]
Braces	0 ± 0 [0]	0 ± 0 [0]	763 ± 1655 [0]	442 ± 818 [0]	545 ± 4060 [0]	319 ± 981 [0]
Pediatric wheelchair (tilt-in-space)	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	191 ± 552 [0]	0 ± 0 [0]	0 ± 0 [0]
Pediatric wheelchair	0 ± 0 [0]	0 ± 0 [0]	176 ± 607 [0]	350 ± 1445 [0]	0 ± 0 [0]	69 ± 431 [0]
Manual adult wheelchair, walker, or cane	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]	0 ± 0 [0]

DME durable medical equipment, SD standard deviation, SMA spinal muscular atrophy, US United States

aCosts for procedures recorded on the same claim as an indicator of treatment with nusinersen or onasemnogene abeparvovec were excluded. Costs were measured from the index date until (1) the last observed month of clinical activity, (2) date of nusinersen reinitiation after discontinuation, (3) an indicator of treatment with onasemnogene abeparvovec, or (4) the end of data availability (i.e., November 30, 2019), whichever occurred first

bInpatient costs included costs of medical procedures received in an inpatient setting and facility costs. Facility costs were imputed using hospital-adjusted expenses per inpatient day for each US state reported by the Henry J. Kaiser Family Foundation; the facility costs (from the institutional perspective; i.e., charged amounts) were imputed based on patient’s respective US state and the length of inpatient stay (https://www.kff.org/health-costs/state-indicator/expenses-per-inpatient-day)

Discussion

Real-world data supporting the efficacy of nusinersen beyond what has been demonstrated in clinical trials are limited. Lavie and colleagues, in one of the few studies to report real-world data for patients with SMA, prospectively collected records from patients with SMA type 1 to investigate respiratory support requirements in those treated with nusinersen; however, this study was limited to only 20 SMA type 1 patients and did not evaluate adherence to nusinersen [27].

Investigation of adherence for SMA treatments is especially necessary because nusinersen is administered intrathecally within set time intervals over patients’ lifetimes, and treatment may pose logistical challenges for patients and their caregivers. Among these challenges are risks related to anesthesia for intrathecal delivery and costs for surgical administration.

In our study of claims data in the United States, we found frequent deviations from the recommended nusinersen dosing schedule across SMA types 1, 2, and 3. The reasons for non-adherence may have had to do with the described logistical challenges for the patient (e.g., traveling to sites for treatment, scheduling time off of work, or finding child care for unaffected siblings) or the patient’s health on a day of planned treatment. These barriers, while understandable, often result in treatment delays that, in this patient population, may result in loss of motor neuron function and disease progression. In addition, non-adherence to treatment may increase health care costs, especially for patients with chronic conditions [14]. For example, non-adherence leads to poorer outcomes (e.g., respiratory illness requiring hospitalization), which result in increased ancillary health care utilization and expenditures related to the underlying disease [18, 19].

Several barriers can affect caregiver adherence to long-term care, including increased dependency on other people, increased presence of siblings or other people living in the household, restrictions on activities of daily living, transportation challenges, lack of knowledge about the disease and/or the medication, concerns about the effectiveness of the treatment, fear about adverse effects, poor prognosis, and poor communication with care providers [28-30]. Strategies to improve adherence include quickly detecting non-adherence (e.g., missed appointments) as well as identifying barriers to adherence [11]. Patient and family education on the importance of adherence is also critical.

There are several limitations of our analysis that should be acknowledged. In this retrospective study, cause-and-effect determinations could not be ascertained, and the small sample size limited generalizations across patient populations. Moreover, there were no statistical analyses for determining factors that may have affected adherence or discontinuation of treatment. Patients were observed over a limited time. Therefore, the patterns observed may not have been constant or consistent. Diagnosis codes captured in the data reflect diagnoses recorded on medical claims for billing purposes and may have been erroneous or incomplete. Further studies with longer follow-up, larger sample sizes, and statistical comparisons are warranted.

Because this study was completed prior to the SARS-CoV2 pandemic, related public health protocols or other factors that might be attributed to the pandemic (e.g., aversion to travel, hesitancy regarding in-clinic procedures) did not confound our analysis.

Conclusions

In conclusion, our analysis of US claims data indicated that discontinuation and non-adherence to nusinersen treatment are prevalent, and associated with greater frequency of comorbidities, greater HCRU, and increased costs for patients. Treatment delays for patients with SMA may result in loss of motor neuron function, disease progression, and increased HCRU and costs. More studies are needed to evaluate the effect of adherence as more patients with SMA are treated with nusinersen. Future research would also be important to evaluate adherence to other treatments for SMA that became available after the completion of this work [24].

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 311 KB)

Real-world data on adherence to nusinersen are limited.

This retrospective claims database analysis studied adherence and discontinuation/persistence for patients with spinal muscular atrophy (SMA) types 1, 2, or 3 treated with nusinersen who completed the loading phase.

The impact of non-adherence or treatment discontinuation on SMA-related comorbidities and health care resource utilization and costs was also assessed.

Discontinuation and non-adherence to nusinersen treatment was associated with a greater rate of comorbidities, greater health care resource use, and increased costs for patients.