Plasma chitotriosidase activity in Gaucher disease patients who have been treated either by bone marrow transplantation or by enzyme replacement therapy with alglucerase

1997 ◽  
Vol 20 (4) ◽  
pp. 595-602 ◽  
Author(s):  
E. Young ◽  
C. Chatterton ◽  
A. Vellodi ◽  
B. Winchester
Keyword(s):  
Bone Marrow ◽  
Bone Marrow Transplantation ◽  
Enzyme Replacement Therapy ◽  
Replacement Therapy ◽  
Marrow Transplantation ◽  
Gaucher Disease ◽  
Enzyme Replacement ◽  
Chitotriosidase Activity

Bone marrow involvement in Gaucher disease at MRI : what long-term evolution can we expect under enzyme replacement therapy?

2015 ◽  
Vol 25 (10) ◽  
pp. 2969-2975 ◽  
Author(s):  
Benjamin Fedida ◽  
Sébastien Touraine ◽  
Jerôme Stirnemann ◽  
Nadia Belmatoug ◽  
Jean-Denis Laredo ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Enzyme Replacement Therapy ◽  
Replacement Therapy ◽  
Gaucher Disease ◽  
Bone Marrow Involvement ◽  
Long Term Evolution ◽  
Enzyme Replacement ◽  
Term Evolution

Bone marrow relaxation times in Gaucher disease before and after enzyme replacement therapy

1997 ◽  
Vol 7 (4) ◽  
pp. 486-491 ◽  
Author(s):  
S. Magnaldi ◽  
R. Longo ◽  
M. Ukmar ◽  
M. Zanatta ◽  
M. Bottega ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Enzyme Replacement Therapy ◽  
Replacement Therapy ◽  
Gaucher Disease ◽  
Relaxation Times ◽  
Enzyme Replacement ◽  
Before And After

scholarly journals Evaluation of the efficacy and safety of the biosimilar drug Glurazyme (imiglucerase) in patients with Gaucher disease type 1

2020 ◽  
Vol 65 (1) ◽  
pp. 8-23
Author(s):  
E. P. Sysoeva ◽  
R. V. Ponomarev ◽  
K. A. Lukina ◽  
R. B. Chavynchak ◽  
S. B. Korotkova ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Enzyme Replacement Therapy ◽  
Replacement Therapy ◽  
Gaucher Disease ◽  
Hemoglobin Concentration ◽  
Efficacy And Safety ◽  
Reference Drug ◽  
Treatment Groups ◽  
Enzyme Replacement

Background. Gaucher disease (GD) is a rare hereditary condition, which represents the most common form of lysosomal storage diseases. Enzyme replacement therapy (ERT) with recombinant glucocerebrosidase is used for the treatment of type 1 and type 3 GD. Imiglucerase (recombinant glucocerebrosidase) is the first biotechnological ERT medication possessing confirmed clinical efficacy and safety.Aim. To compare the efficacy and safety of the biosimilar drug Glurazyme and the reference drug Cerezyme during ERT therapy in patients with type 1 GD.Materials and methods. Thirty patients aged from 19 to 63 years (33 ± 9.7 years) with a stable course of type 1 GD were enrolled in the study. The patients were randomly divided into two equal treatment groups, one of which received Glurazyme and the other received the reference drug Cerezyme. In both groups, the drugs were used in doses of 15–40 U/kg intravenously once every 14 days for 52 weeks.Results. At the end of the study, at week 52 (primary endpoint of efficacy), both groups demonstrated a similar increase in hemoglobin concentration compared to the baseline data. In both groups, the average increase in hemoglobin concentration was 4.8 g/l, with this parameter varying between the groups by 0.1 g/l. At week 52, the calculated 95% confidence interval for the difference in hemoglobin concentration did not cross the non-inferiority margin of 18 g/l, which had been specified as the lower level of drug efficacy. This led to the conclusion that the studied drug Glurazyme is not inferior to Cerezyme in terms of efficacy. A comparison of the treatment groups by secondary endpoints of efficacy revealed: no decrease in hemoglobin concentration by more than 20 % in both groups; no differences between the groups by the number of patients with a change in platelet concentration relative to the baseline values; no increase in the spleen and liver volume by more than 20 and 10 %, respectively, in both groups. The doses of the drug under study and the reference drug remained unchanged during the research. The concentration of chemokine CCL-18 decreased slightly in 10 patients (64.3 %) and 6 patients (40 %) in the Glurazyme group and the Cerezyme group, respectively. The proportion of patients with improved physical and mental health components was 57.1 and 57.1 %, respectively, in the Glurazyme group compared to 73.3 and 60 %, respectively, in the Cerezyme group. Changes in the state of the bone tissue and the reserves of accumulated metabolites in the bone marrow showed a similar decrease in the severity of bone marrow infiltration in both groups.Conclusions. Glurazyme and Cerezyme showed comparable parameters of efficacy and safety in patients with GD type 1 during long-term enzyme replacement therapy.

Superior effects of high-dose enzyme replacement therapy in type 1 Gaucher disease on bone marrow involvement and chitotriosidase levels: a 2-center retrospective analysis

Blood ◽  
2006 ◽  
Vol 108 (3) ◽  
pp. 830-835 ◽  
Author(s):  
Maaike de Fost ◽  
Carla E. M. Hollak ◽  
Johanna E. M. Groener ◽  
Johannes M. F. G. Aerts ◽  
Mario Maas ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Enzyme Replacement Therapy ◽  
Replacement Therapy ◽  
Gaucher Disease ◽  
Bone Marrow Involvement ◽  
Median Dose ◽  
Long Term Outcome ◽  
Enzyme Replacement ◽  
Type 1 Gaucher Disease

AbstractDosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate and varies from 15 to 130 U/kg/mo, making a huge economic difference of US $70 000 to US $380 000 (€55 000-300 000) per patient per year. To investigate whether this difference in dosing ultimately translates into a different response, we retrospectively compared long-term outcome of ERT at 2 large European treatment centers, Academic Medical Center, Amsterdam, The Netherlands (n = 49, median dose, 15-30 U/kg/4 wks) and Heinrich-Heine University, Duesseldorf, Germany (n = 57, median dose, 80 U/kg/4 wks). These adult cohorts had a similar genetic background. All follow-up parameters were matched separately at baseline, to avoid bias with respect to disease severity. Improvement in hemoglobin, platelet count, and hepatosplenomegaly was not significantly different between both cohorts, whereas plasma chitotriosidase and bone marrow involvement by magnetic resonance imaging improved more quickly and was more pronounced in the higher-dosed group. Major bone complications rarely occurred in both groups. In conclusion, different dosing regimens of ERT do not affect outcome of hematologic and visceral parameters, but higher dosing leads to accelerated decrease of chitotriosidase and better objective bone response in adult type 1 Gaucher disease.

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