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Prospective open-label trial with rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy not responding to conventional immune therapies
by
Doneddu, Pietro Emiliano
, Germano, Francesco
, Benedetti, Luana
, Peci, Erdita
, Falzone, Yuri Matteo
, Gallia, Francesca
, Lleixà, Cinta
, Fazio, Raffaella
, Nobile-Orazio, Eduardo
, Liberatore, Giuseppe
, Bianchi, Elisa
, Cocito, Dario
, Giannotta, Claudia
in
Adult
/ Aged
/ Antibodies
/ Antigens
/ Apheresis
/ Birth control
/ Female
/ Humans
/ Immunoglobulins
/ Immunologic Factors - therapeutic use
/ Immunotherapy
/ Male
/ Middle Aged
/ Monoclonal antibodies
/ Neural Conduction - drug effects
/ NEUROIMMUNOLOGY
/ Neuromuscular
/ NEUROPATHY
/ Plasma
/ Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - drug therapy
/ Prospective Studies
/ Proteins
/ Rituximab - therapeutic use
/ Side effects
/ Steroids
/ Treatment Outcome
2024
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Prospective open-label trial with rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy not responding to conventional immune therapies
by
Doneddu, Pietro Emiliano
, Germano, Francesco
, Benedetti, Luana
, Peci, Erdita
, Falzone, Yuri Matteo
, Gallia, Francesca
, Lleixà, Cinta
, Fazio, Raffaella
, Nobile-Orazio, Eduardo
, Liberatore, Giuseppe
, Bianchi, Elisa
, Cocito, Dario
, Giannotta, Claudia
in
Adult
/ Aged
/ Antibodies
/ Antigens
/ Apheresis
/ Birth control
/ Female
/ Humans
/ Immunoglobulins
/ Immunologic Factors - therapeutic use
/ Immunotherapy
/ Male
/ Middle Aged
/ Monoclonal antibodies
/ Neural Conduction - drug effects
/ NEUROIMMUNOLOGY
/ Neuromuscular
/ NEUROPATHY
/ Plasma
/ Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - drug therapy
/ Prospective Studies
/ Proteins
/ Rituximab - therapeutic use
/ Side effects
/ Steroids
/ Treatment Outcome
2024
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Prospective open-label trial with rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy not responding to conventional immune therapies
by
Doneddu, Pietro Emiliano
, Germano, Francesco
, Benedetti, Luana
, Peci, Erdita
, Falzone, Yuri Matteo
, Gallia, Francesca
, Lleixà, Cinta
, Fazio, Raffaella
, Nobile-Orazio, Eduardo
, Liberatore, Giuseppe
, Bianchi, Elisa
, Cocito, Dario
, Giannotta, Claudia
in
Adult
/ Aged
/ Antibodies
/ Antigens
/ Apheresis
/ Birth control
/ Female
/ Humans
/ Immunoglobulins
/ Immunologic Factors - therapeutic use
/ Immunotherapy
/ Male
/ Middle Aged
/ Monoclonal antibodies
/ Neural Conduction - drug effects
/ NEUROIMMUNOLOGY
/ Neuromuscular
/ NEUROPATHY
/ Plasma
/ Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - drug therapy
/ Prospective Studies
/ Proteins
/ Rituximab - therapeutic use
/ Side effects
/ Steroids
/ Treatment Outcome
2024
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Prospective open-label trial with rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy not responding to conventional immune therapies
Journal Article
Prospective open-label trial with rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy not responding to conventional immune therapies
2024
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Overview
BackgroundTo evaluate the efficacy of rituximab in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) patients not responding to conventional immune therapies.MethodsAn open-label, prospective exploratory study was conducted with intravenous rituximab on 17 CIDP patients who had not responded to at least two first-line therapies. The primary endpoint was to determine the proportion of patients who showed improvement 6 months after rituximab therapy. The percentage of responders to rituximab, along with a 95% CI, was reported and compared with the 30% response rate after other immunosuppressive drugs previously documented in the literature.Results13 of the 17 treated patients (76.5%) showed improvement at 6 months (95% CI 50.1 to 93.2). Among the 14 patients who completed the 12-month follow-up (2 were lost to follow-up after showing improvement at months 8 and 10, and 1 deteriorated at 6 months), 13 (92.9%) demonstrated improvement at 12 months (95% CI 66.1 to 99.8). Nerve conduction parameters improved by at least 20% in two nerves in 6 out of 15 (40%) patients at 6 months and in 7 out of 13 (53.9%) at 12 months. None of the treated patients withdrew from the study due to side effects. There was a significant reduction of circulating CD19+ cells 15 days, 2, 6 and 12 months after treatment.ConclusionRituximab seems to be a safe therapy in most patients with CIDP not responding to conventional immune therapies. The high percentage of patients who improved in this study suggests a possible positive effect of rituximab which is worth investigating in future randomised controlled clinical trials.Trial registration numberNCT05877040.
Publisher
BMJ Publishing Group Ltd,BMJ Publishing Group LTD
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