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Randomized trial of three IVIg doses for treating chronic inflammatory demyelinating polyneuropathy

Authors :
Cornblath, David R.
Van Doorn, Pieter A.
Hartung, Hans Peter
Merkies, Ingemar S.J.
Katzberg, Hans D.
Hinterberger, Doris
Clodi, Elisabeth
Cornblath, David R.
Van Doorn, Pieter A.
Hartung, Hans Peter
Merkies, Ingemar S.J.
Katzberg, Hans D.
Hinterberger, Doris
Clodi, Elisabeth
Source :
Cornblath , D R , Van Doorn , P A , Hartung , H P , Merkies , I S J , Katzberg , H D , Hinterberger , D & Clodi , E 2022 , ' Randomized trial of three IVIg doses for treating chronic inflammatory demyelinating polyneuropathy ' , Brain , vol. 145 , no. 3 , pp. 887-896 .
Publication Year :
2022

Abstract

Intravenous immunoglobulin treatment for chronic inflammatory demyelinating polyneuropathy usually starts with a 2.0 g/kg induction dose followed by 1.0 g/kg maintenance doses every 3 weeks. No dose-ranging studies with intravenous immunoglobulin maintenance therapy have been published. The Progress in Chronic Inflammatory Demyelinating polyneuropathy (ProCID) study was a prospective, double-blind, randomized, parallel-group, multicentre, phase III study investigating the efficacy and safety of 10% liquid intravenous immunoglobulin (Panzyga®) in patients with active chronic inflammatory demyelinating polyneuropathy. Patients were randomized 1:2:1 to receive the standard intravenous immunoglobulin induction dose and then either 0.5, 1.0 or 2.0 g/kg maintenance doses every 3 weeks. The primary end point was the response rate in the 1.0 g/kg group, defined as an improvement ≥1 point in adjusted Inflammatory Neuropathy Cause and Treatment score at Week 6 versus baseline and maintained at Week 24. Secondary end points included dose response and safety. This trial was registered with EudraCT (Number 2015-005443-14) and clinicaltrials.gov (NCT02638207). Between August 2017 and September 2019, the study enrolled 142 patients. All 142 were included in the safety analyses. As no post-infusion data were available for three patients, 139 were included in the efficacy analyses, of whom 121 were previously on corticosteroids. The response rate was 80% (55/69 patients) [95% confidence interval (CI): 69-88%] in the 1.0 g/kg group, 65% (22/34; CI: 48-79%) in the 0.5 g/kg group, and 92% (33/36; CI: 78-97%) in the 2.0 g/kg group. While the proportion of responders was higher with higher maintenance doses, logistic regression analysis showed that the effect on response rate was driven by a significant difference between the 0.5 and 2.0 g/kg groups, whereas the response rates in the 0.5 and 2.0 g/kg groups did not differ significantly from the 1.0 g/kg group. Fifty-six per cent of al

Details

Database :
OAIster
Journal :
Cornblath , D R , Van Doorn , P A , Hartung , H P , Merkies , I S J , Katzberg , H D , Hinterberger , D & Clodi , E 2022 , ' Randomized trial of three IVIg doses for treating chronic inflammatory demyelinating polyneuropathy ' , Brain , vol. 145 , no. 3 , pp. 887-896 .
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1379333285
Document Type :
Electronic Resource