Olipudase alfa is a recombinant human acid sphingomyelinase (ASM) enzyme replacement therapy (ERT) for non-central-nervous-system manifestations of acid sphingomyelinase deficiency (ASMD). We report 2-year cumulative safety and efficacy data after olipudase alfa treatment in 20 children (four adolescents [12–17 year], nine children [6–11 year], and seven infants/early child [1–5 year]) with baseline splenomegaly and growth deficits who completed the 1-year ASCEND-Peds clinical trial (NCT02292654) and who continue to receive olipudase alfa in a long-term study (NCT02004704). Efficacy endpoints include spleen and liver volumes, diffusing capacity of the lung for carbon monoxide (DLCO), high-resolution computed tomography (HRCT) lung imaging, lipid profiles, liver function tests, and height Z-scores.
All 20 former ASCEND-Peds patients completed at least 2 years of olipudase alfa treatment. No patient discontinued and no new safety issue arose during the second year of treatment; 99% of adverse events were mild or moderate. During year 2, one patient had two treatment-related serious events of hypersensitivity that resolved. Mean reductions from baseline in spleen and liver volumes were 61% and 49%, respectively (p < 0.0001) and mean percent-predicted-DLCO increased by 46.6% (p < 0.0001) in nine patients who performed the test at baseline. Lipid profiles and elevated liver transaminase levels that improved or normalized by 1 year remained stable. Mean height Z-scores improved in all age groups (mean change from baseline 1.17, P < 0.0001).
Olipudase alfa was generally well-tolerated during 2 years of treatment. Improvements in clinically relevant disease endpoints observed during the first year of treatment were maintained or augmented in the second year.
Acid sphingomyelinase deficiency (ASMD) (historically known as Niemann-Pick disease [NPD] types A [OMIM257200], B [OMIM607616], A/B) is an inherited lysosomal storage disease characterized by deficient activity of the enzyme acid sphingomyelinase (ASM). Deficiency of ASM results in accumulation of glycosphingolipids, including the primary substrate sphingomyelin, in tissue macrophages and hepatocytes, and in the most severe form of ASMD, in neurons [1, 2]. Manifestations include hepatosplenomegaly and interstitial lung disease (ILD) accompanied by thrombocytopenia, bleeding/bruising, dyslipidemia, growth deficits and delayed puberty, osteoporosis/osteopenia, liver dysfunction with progressive fibrosis, and cardiac disease [3, 4]. ASMD subtypes reflect a disease spectrum ranging from ASMD type A (infantile neurovisceral disease)  that is uniformly fatal within the first 3 years of childhood, to chronic forms ASMD type B (chronic visceral) and ASMD type A/B (chronic neurovisceral) that lack predominant neurodegeneration and frequently present with visceral symptoms in childhood. Chronic forms of ASMD are associated with significant morbidity and sometimes early mortality due to respiratory or liver failure [6,7,8,9]. Supportive care is used for symptom management in the absence of an approved disease-modifying therapy .
Olipudase alfa (Xenpozyme®) is a recombinant human ASM enzyme replacement therapy (ERT) approved for the treatment of the non-central nervous system manifestations of ASMD in children and adults. Olipudase alfa is well-tolerated in adults [11,12,13] and pediatric  patients with chronic ASMD after a within-patient dose escalation regimen designed to gradually debulk tissue sphingomyelin [15, 16]. Olipudase alfa was associated with clinically significant improvements in disease pathology and multiple endpoints compared with placebo in adults with ASMD . In pediatric patients with chronic ASMD, an open label single-arm study demonstrated improvements across a range of endpoints after 1 year of treatment . This paper reports on the safety and clinical outcomes data for these pediatric patients ranging in age from infancy to adolescence who have received olipudase alfa infusions every 2 weeks for 24 months.
As described previously, 20 pediatric patients with confirmed ASMD, spleen volume ≥ 5 multiples of normal (MN), and height Z-score ≤ − 1 participated in the open-label, single arm ASCEND-Peds trial . The study included patients with ASMD types B or A/B and no patients with ASMD type A were enrolled. After the 52-week (efficacy)/64-week (safety) primary analysis periods, all 20 patients have continued olipudase alfa treatment in a long-term study (trial registration NCT02004704; EudraCT2013-000051-40). Institutional Review Boards at study sites approved the protocol and patients/parents provided written consent.
Olipudase alfa infusions
Olipudase alfa infusions were administered every 2 weeks. All patients underwent individualized dose escalation over a minimum of 16 weeks in the ASCEND-Peds trial and achieved the target maintenance dose of 3 mg/kg as described previously .
All safety and efficacy outcomes represent cumulative patient data through 24 months from olipudase alfa initiation. Adverse events were summarized by incidence, seriousness, severity, and relationship to olipudase alfa treatment. Clinical parameters (spleen volume and liver volume in multiples of normal [MN], where normal spleen and liver volumes are considered to be 0.2% and 2.5% of body weight, respectively , percent predicted diffusing capacity of the lung for carbon monoxide [DLCO] adjusted for hemoglobin, volumetric lung function tests, high-resolution computed tomography [HRCT] lung imaging scores, platelet counts, liver function, plasma lipid profiles, height Z-scores) and biomarkers reflecting the activity of ASMD (plasma chitotriosidase activity [normalized, µmol/L/hr], plasma lyso-sphingomyelin [μg/L]) were evaluated as described previously . X-ray of the left hand, fingers and wrist were used to determine bone age compared to actual age using the Greulich and Pyle atlas .
Analyses were performed overall and by baseline age group. Descriptive statistics with standard deviations were used for continuous variables and for concentration–time data. Categorical variables were summarized using frequencies and percents. Change and percent change from baseline were analyzed with the analysis of covariance (ANCOVA) method adjusting for baseline value and without multiplicity adjustment except for HRCT scores, for which a linear regression model was used to assess change from baseline adjusted by baseline HRCT scores. P values from the various tests are presented for the mean or least square (LS) mean change (or percent change) from baseline to 24 months, and all are nominal.
Patient baseline characteristics
Twenty enrolled patients completed the primary analysis period of the ASCEND-Peds trial and continued olipudase alfa treatment in the long-term study (Fig. 1). Baseline characteristics have been previously published  and are shown in Additional file 1: Table S1. Age at symptom onset ranged from 1.9 months to 3.9 years and presenting symptoms at disease onset included splenomegaly (90%), hepatomegaly (90%), respiratory diseases (35%), thrombocytopenia (25%) and excessive bleeding and bruising (10%). Age at trial enrollment ranged from 1 to 17 years, males and females were equally represented, and the majority were Caucasian. At baseline, 12 patients (60%) had severe splenomegaly (> 15 MN).
Olipudase alfa dosing
The median time (min, max) to achieve the target dose during the primary ASCEND-Peds 64-week study was 18 weeks (16, 50). All patients maintained the target dose of 3 mg/kg during the second year of treatment. One patient had a temporary dose reduction during week 67 of treatment due to adverse events of sore throat, pharyngotonsillitis, bronchitis, and fever unrelated to olipudase alfa treatment.
There were no permanent treatment discontinuations or withdrawals from the study during 24 months of olipudase alfa treatment. Treatment-emergent adverse events occurring during the primary 64-week safety period have been described in detail previously . No new safety issues occurred during the second year of olipudase alfa treatment and 99% (1070/1077) of all treatment-emergent adverse events from first dose through month 24 were reported as mild (960/1077, 89%) or moderate (110/1077, 10%).
As reported for the primary safety period , the most common adverse events considered related to olipudase alfa were pyrexia, vomiting, urticaria, and headache, most of which were mild infusion-associated reactions (IARs) as shown in Table 1. IARs were reported for 13 patients during 24 months of olipudase alfa infusions. The number of IARs and number of patients with IARs peaked by 6 months and subsequently steadily decreased over time as shown in Fig. 2. Among 115 IAR events occurring from first dose, 99 (86%) were reported as mild, 15 (13%) as moderate and 1 (0.9%) as severe (an anaphylactic reaction in a patient during the second month of treatment as previously reported ). Among IARs occurring in the second year of treatment, none were severe, 19/23 (83%) were reported as mild, and 4/23 (17%) were reported as moderate.
In addition to three patients with serious adverse events related to treatment that were reported during the 64-week primary analysis period and described previously , a 6-year-old patient had two serious adverse events consisting of IARs of mild hypersensitivity reactions (sneezing, flushing, facial edema, and hives) during weeks 68–70 that resolved with supportive medication and temporary interruption of the olipudase alfa infusions (completed).
There were no clinically significant abnormalities in laboratory findings, vital signs, electrocardiograms, or echocardiograms during the second year of treatment.
Spleen and liver volume
Splenomegaly and hepatomegaly were moderate or severe  at baseline and improved in all patients, with the largest magnitude of improvement during the first 6 months of treatment  followed by further incremental improvement over the subsequent 18 months (Fig. 3A, B for spleen and 3C and D for liver). Mean spleen volume decreased from 19.0 ± 8.8 MN at baseline to 7.2 ± 3.3 MN at 24 months (LS mean percent difference ± SEM − 60.9 ± 1.9%, p < 0.0001). Individual decreases in spleen volume ranged from 41.6 to 76.2%. All patients achieved spleen volumes in the mild to moderate  range by 24 months except for one patient with severe baseline splenomegaly whose 24-month value was borderline moderate at 15.1 MN. Decreases in spleen volume over time were similar across the different pediatric age groups (Fig. 3B).
Similar patterns were observed for hepatomegaly (Fig. 3C). Mean liver volume decreased from 2.7 ± 0.7 MN at baseline to 1.3 ± 0.2 MN at 24 months (LS mean percent difference ± SEM − 49.0 ± 1.7%, nominal p < 0.0001), with individual decreases ranging from 30.5 to 66.5%. All patients achieved liver volumes in the mild to moderate range  by 24 months. Decreases in liver volume over time were similar across the different pediatric age groups (Fig. 3D).
Summary data for mean decreases in organomegaly over time and percent change from baseline are provided in Additional file 1: Table S2.
Among nine patients ≥ 5 years of age able to perform lung function tests, baseline percent predicted DLCO was severely impaired in one patient, moderately impaired in four, and mildly impaired in four (Fig. 3E) . Mean baseline percent predicted DLCO was 54.8 ± 14.2 (moderate impairment ). DLCO improved in all nine patients with baseline data by 24 months, with a LS mean percent difference ± SEM of 46.4 ± 4.1% (p = 0.0039). Individual changes from baseline ranged from 17% to 85.3%, with eight patients improving to no or mild impairment at 24 months, and one adolescent patient improving from severe impairment at baseline to moderate at 24 months (Fig. 3E). Mean percent predicted DLCO for 14 patients with data at 24 months was 82.8 ± 27.5 (no impairment ). Mean percent predicted DLCO stratified by age category showed similar improvements over time in both the child and adolescent groups (Fig. 3F). Summary data are provided in Additional file 1: Table S2.
Lung volumetric tests included forced vital capacity (FVC) and total lung capacity (TLC) among those able to perform lung function tests. The mean percent predicted values over time are shown in Additional file 1: Fig. S1. The mean percent predicted value improved from 77.4 ± 16.3% at baseline to 89.6 ± 23.4% at 24 months (LS mean difference ± SEM 22.6 ± 6.2%, p = 0.0081) for FVC and from 86.8 ± 23.3% to 122.6 ± 22.8% (LS mean difference ± SEM 52.9 ± 7.1, p = 0.002) for TLC.
As previously described , pulmonary imaging of lung regions was scored qualitatively by central readers for ground glass appearance, ILD, and reticulonodular density based percent of lung volume affected, where 0 = no disease; 1 = mild (≤ 25% of lung volume); 2 = moderate (26–50%); 3 = severe (51–100%). HRCT images and scores for ground glass appearance at baseline, 12 months and 24 months are shown in Fig. 4A for the patient (baseline age 7 years) who had the worst ground glass score at baseline. In this patient, ground glass opacity resolved with a score of 0 at 24 months.
At baseline, ground glass appearance scores were moderate to severe and ILD and reticulonodular density scores were mild. All three mean scores improved with 12 months of olipudase alfa treatment , and these improvements were maintained or further increased after 24 months (Fig. 4B). At 24 months, mean ± SD ground glass appearance score decreased from baseline by 0.44 points from 0.79 ± 0.75 to 0.31 ± 0.77 at 24 months (p = 0.0012), mean ILD score decreased by 0.70 ± 0.63 from 2.49 ± 0.74 to 1.87 ± 0.83 (p = 0.0001), and mean reticulonodular density score decreased by 0.58 ± 1.18 from 0.62 ± 1.1 to 0.07 ± 0.22 (p = 0.0463).
Individual height Z-scores over time are shown in Fig. 5A. Baseline height Z-scores ranged from − 3.8 to − 1.0 with a median of − 2.0 (mean − 2.1 ± 0.8). Ten patients (50%) met the criteria for short stature (i.e., height 2 or more standard deviations below the mean for age , equating to a Z-score of − 2 or less). Mean height Z-score improved from − 2.14 ± 0.84 at baseline to − 0.99 ± 0.88 at 24 months (LS mean difference ± SEM 1.17 ± 0.12, p < 0.0001) with individual scores ranging from − 2.7 to 0.3 (median − 0.9; mean − 1.0 ± 0.88). The proportion of patients with short stature at 24 months was 3/16 (19%). Mean height Z-score over time stratified by age category showed similar improvements over time (Fig. 4B).
For 19 patients with baseline and 24-month bone age data determined from wrist x-rays, the mean delay in bone age decreased from 25.6 ± 18.1 months to 17.0 ± 16.0 months after 2 years of olipudase alfa treatment (LS mean difference ± SEM 8.6 ± 2.8 months, p = 0.0065).
Improvements in liver function tests and plasma lipid profiles observed at 12 months were maintained or further improved at 24 months (Additional file 1: Figs. S2 and S3, respectively), with mean values maintained within normal ranges. Mean baseline platelet counts reflected mild thrombocytopenia  and were improved at 24 months by 35.9 ± 32.4 × 109/L (p = 0.0014) from 137.7 ± 62.3 × 109/L to 166.9 ± 64.9 × 109/L.
Both plasma lyso-sphingomyelin, the deacylated form of sphingomyelin and plasma chitotriosidase activity, a biomarker of activated macrophages, were elevated at baseline (mean values > 60 and > 6 times the upper limit of normal [ULN], respectively) and decreases reported by 6 months were maintained at 12 months . At 24 months there was a mean reduction of pre-infusion plasma lyso-sphingomyelin of 87% and levels were near the ULN (Additional file 1: Fig. S4A). Plasma chitotriosidase activity was also close to the ULN at 24 months, reflecting a 76% reduction from baseline (Additional file 1: Fig. S4B).
In the absence of disease-specific treatment, natural history studies indicate that disease burden and mortality risk increase over time in children and adolescents with chronic forms of ASMD [4, 9, 21,22,23], with liver and lung disease  identified as major contributors to early death [7, 8]. The 2-year results of this trial demonstrate that a disease-modifying therapy such as olipudase alfa can substantially alleviate the disease burden in children from infancy through adolescence with chronic forms of ASMD.
Step-wise dose escalation is used for patients in olipudase alfa clinical trials [12, 14] to minimize adverse events arising from rapid production of high concentrations of bioactive catabolites and depletion of the substrate sphingomyelin [15, 16]. With this dose escalation regimen, metabolite levels and disease biomarkers decrease following treatment initiation, confirming olipudase alfa’s mechanism of action [12, 14]. Plasma levels of the sphingomyelin metabolite lyso-sphingomyelin levels shown to decrease over the first three months of olipudase alfa infusions in pediatric patients  remained stable at near normal values through 24 months of treatment. Activity of chitotriosidase, a biomarker of activated macrophages that was elevated at baseline decreased to near normal levels by 6 months , was stable through 24 months.
Olipudase alfa ERT was well tolerated over 24 months of treatment and there were no permanent discontinuations or study withdrawals due to adverse events. Most treatment-related events were mild to moderate IARs occurring primarily in the first 6 months of treatment and becoming less frequent over time, which is a typical observation with ERT . IAR events occurring with olipudase alfa infusions were managed in some cases with temporary infusion interruptions or dose reductions that did not prevent reaching or maintaining the target olipudase alfa dose.
Olipudase alfa treatment resulted in significant improvements in key disease characteristics known to persist or worsen over time  in untreated pediatric patients of all ages with chronic ASMD. Deterioration in lung function occurs in children with untreated ASMD , and is associated with increased risk of respiratory infections and respiratory failure . Progressive decline in pulmonary function also contributes to early mortality and decreased quality of life [8, 23, 26,27,28]. Lung function and ILD improved in all pediatric patients receiving olipudase alfa. Diffusing capacity of the lung assessed by determining the percent predicted DLCO improved to mild or no impairment by 24 months in eight of nine children with baseline data, and to moderate impairment in one patient with severe impairment at baseline. Improvement in diffusing capacity was supported by pulmonary imaging assessments of ILD with decreases in mean scores for ground glass appearance, ILD, and reticulo nodular density.
A hallmark clinical manifestation of ASMD is moderate to severe organomegaly [8, 9, 29], which occurs early in life in children with chronic ASMD and does not resolve or improve over time . Organomegaly in LSDs and other chronic diseases can impact satiety with consequences on nutrition and development in children [17, 30]. Splenomegaly in ASMD is also associated with increased bleeding risk ; thus, lifestyle modifications are often advised in order to reduce risk of splenic rupture . All pediatric patients had reductions from baseline in spleen and liver volumes of greater than 30% by 24 months.
Other clinical parameters that worsen over time in pediatric patients with ASMD include dyslipidemia [4, 9] and thrombocytopenia . Lipid profiles and platelet counts significantly improved over 12 months of olipudase alfa treatment  and showed additional improvements and normalization by 24 months of treatment. Elevated liver transaminases reflecting ASMD-associated liver pathology in pediatric patients [9, 29] normalized beginning in the first few weeks of olipudase alfa treatment  and remained within normal limits through 24 months.
Short stature is associated with poorer quality of life in children and adults . Growth deficits in children and adolescents with chronic ASMD are common [9, 32, 33], although some patients achieve normal stature, often in association with homozygosity for the SMPD1 variant p.Arg610del [32, 34]. No patient enrolled in the ASCEND-Peds study was homozygous for p.Arg610del and all had growth deficits at baseline per inclusion criteria . Improvements in Z-scores occurred in all patients, and the percentage of children with short stature decreased from 50% at baseline to 19% at 24 months of treatment. Mean bone age, which was delayed compared to actual age at the start of the study, increased over actual age for 19 children.
ERT with olipudase alfa remained well-tolerated through 24 months of treatment in infants/young children, children, and adolescents with chronic ASMD, and treatment was associated with improvements in disease pathology across multiple clinically meaningful endpoints. Importantly, improvements observed during the first year of olipudase alfa treatment were maintained or further improved during the second year of treatment.
Availability of data and materials
Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org.
Acid sphingomyelinase deficiency
Diffusing capacity of the lung for carbon monoxide
Enzyme replacement therapy
Forced fital capacity
High-resolution computed tomography
Infusion associated reaction
Interstital lung disease
Multiples of normal
Standard error of the mean
Total lung capacity
Upper limit of normal
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The authors thank the patients and families, and the research facility clinical staff. Medical writing and editing funded by Sanofi were provided by Patrice C. Ferriola, Ph.D. of KZE PharmAssociates, LLC. Lisa Underhill of Sanofi provided editorial review.
Sanofi was the study sponsor and was involved in the study design, data collection, data analysis, interpretation of data, and collaboration with authors on the writing of the manuscript. All authors had full access to the trial data and are responsible for the data accuracy and interpretation of the results. The corresponding author had final responsibility for submission of the manuscript.
Authors and Affiliations
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, New York, NY, 10029, USA
George A. Diaz
Medical Genetics Service HCPA, Department of Genetics UFRGS, DASA and Casa dos Raros, Porto Alegre, Brazil
Reference Centre of Inherited Metabolic Disease in Femme Mère Enfant Hospital, Hospices Civils of Lyon, Lyon, France
Manchester University National Health Service Trust, St Mary’s Hospital, Manchester, UK
Simon A. Jones
Institute of Clinical Science for Lysosomal Storage Disorders, SphinCS GmbH, Mainz, Germany
GAD contributed substantially to acquisition and interpretation of data, and writing and review of manuscript drafts. RG contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. NG contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. SAJ contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. EM contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. MA contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. PW contributed substantially to acquisition and interpretation of data, and editing and review of manuscript drafts. AY contributed substantially to analysis and interpretation of data, and review of manuscript drafts. JL contributed substantially to analysis and interpretation of data, and review of manuscript drafts. NMA contributed substantially to analysis and interpretation of data, and review of manuscript drafts. YK contributed substantially to analysis and interpretation of data, and review of manuscript drafts.CO-R contributed substantially to design of the study, acquisition and interpretation of data, and writing and review of manuscript drafts. MK contributed substantially to design of the study, interpretation of data, and writing and review of manuscript drafts. All authors read and approved the final manuscript.
Local Institutional Review Boards (IRB) at all study sites approved the protocol (corresponding author’s IRB: Mount Sinai School of Medicine Program for the Protection of Human Subjects1425 Madison Avenue, East Building 4-78, Box 1075 New York, New York 10029) and patients/parents provided written informed consent prior to patient screening. All clinical data were de-identified. The study adhered to the principles set out in the Declaration of Helsinki.
Consent for publication
GAD, SAJ, MS, K. EM, RG, PW, and NG are principal investigators in Sanofi sponsored trials. GAD and SAJ have received honoraria and consulting fees from Sanofi. EM has received research support, honoraria, and consulting fees from Sanofi. RG has received honoraria, consulting fees, speaker fees and travel reimbursement from Sanofi. NG has received honoraria and travel reimbursement from Sanofi. MS has received honoraria, consulting fees, speaker fees and travel reimbursement from Sanofi. PW has participated in advisory boards and received travel reimbursement from Sanofi. AY, JL, NA, YK, CO-R, and MK are employed by Sanofi and may own Sanofi stock.
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. Demographics and baseline characteristics. Table S2. Spleen and Liver Volumes, Percent Predicted DLCO, and height Z-scores at Baseline and 24 Months for by Age Group. Fig. S1. Results for volumetric lung function tests over time. Mean % predicted forced vital capacity (FVC) and total lung capacity (TLC) for overall pediatric population. Fig. S2. Plasma levels of liver enzymes and total bilirubin during treatment with olipudase alfa. Fig. S3. Plasma lipid concentrations during treatment with olipudase alfa. Fig. S4. Pre-infusion Plasma Levels Lyso-Sphingomyelin (A), and Chitotriosidase Activity (B) During Treatment with Olipudase Alfa.
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Diaz, G.A., Giugliani, R., Guffon, N. et al. Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results.
Orphanet J Rare Dis17, 437 (2022). https://doi.org/10.1186/s13023-022-02587-0