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Relapsing and primary progressive multiple sclerosis: Ocrelizumab infusion experience


Ocrelizumab ( Ocrevus ) is an infusible humanized monoclonal antibody that selectively depletes CD20+ B cells.
Infusion-related reactions ( IRRs ) were summarized from the OPERA I, OPERA II, and ORATORIO trials for relapsing and primary progressive multiple sclerosis ( MS ).

OPERA I and OPERA II were identical, randomized, double-blind, active-controlled trials that enrolled patients with relapsing multiple sclerosis ( RMS ).
Patients in the Ocrelizumab group initially received two 300-mg intravenous ( IV ) infusions separated by 14 days ( on days 1 and 15 ); subsequent doses were administered as single 600-mg IV infusions.
Ocrelizumab-treated patients also received subcutaneous ( SC ) placebo injections 3 times weekly.
Patients in the active comparator group received SC injections of Interferon ( IFN ) beta-1a 3 times weekly, as well as placebo infusions on days 1 and 15 and weeks 24, 48, and 72.

ORATORIO was a randomized, parallel-group, double-blind, placebo-controlled study that enrolled patients with primary progressive multiple sclerosis ( PPMS ).
As in the OPERA studies, patients in the Ocrelizumab group initially received two 300-mg infusions separated by 14 days; however, ORATORIO patients continued to receive this divided-dose regimen throughout the study.
The ORATORIO control group received IV placebo.

Prior to each infusion, all patients in the OPERA and ORATORIO studies were pretreated with 100 mg IV Methylprednisolone; additional prophylactic treatment with analgesics, antipyretics, and/or an IV or oral antihistamine was optional.

Infusion-related reactions were defined as adverse events that occurred during or within 24 h of IV infusion of Ocrelizumab or placebo.

Safety analyses included 1651 patients with relapsing multiple sclerosis from OPERA I and OPERA II ( Ocrelizumab, n = 825; Interferon beta-1a, n = 826 ) and 725 patients with primary progressive multiple sclerosis from ORATORIO ( Ocrelizumab, n = 486; placebo, n = 239 ).

Across studies, IRRs were reported in 34.3% ( vs 9.7% with Interferon beta-1a ) and 39.9% ( vs 25.5% with placebo ) of Ocrelizumab-treated patients in the pooled OPERA and ORATORIO populations, respectively.

The majority of IRRs were mild to moderate in the OPERA ( Ocrelizumab, 92.6%; Interferon beta-1a, 98.8% ) and ORATORIO ( Ocrelizumab, 96.9%; placebo, 93.4% ) studies.
IRRs most commonly occurred with the first infusion.

Severe IRRs were reported in 2.4% of Ocrelizumab-treated patients in the OPERA studies ( vs 0.1% with Interferon beta-1a ) and 1.2% of Ocrelizumab-treated patients in ORATORIO ( vs 1.7% with placebo ).

Two serious IRRs occurred across the OPERA studies, both of which occurred with the initial infusion. The first event occurred in an Interferon beta-1a-treated patient in association with the initial infusion of IV placebo and consisted of severe balance disorder, dizziness, flushing, and hypoesthesia. The second event was a life-threatening reaction ( bronchospasm ) that occurred in an Ocrelizumab-treated patient 15 min after the infusion started.
Frequently reported IRR symptoms included pruritus, rash, throat irritation, and flushing.
Premedication use, particularly antihistamines, was associated with fewer IRRs.

In conclusion, findings from the OPERA I, OPERA II, and ORATORIO trials have shown that IRRs were the most frequently reported adverse events with Ocrelizumab, were mostly mild to moderate in severity, were reduced with appropriate pretreatment, and decreased with subsequent dosing.
IRRs that did occur were effectively managed through infusion rate adjustment and symptomatic treatment. ( Xagena )

Mayer L et al, Mult Scler Relat Disord 2019; 30: 236-243

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