Rituximab Dosing for Hypersensitivity Pneumonitis
For patients with hypersensitivity pneumonitis requiring rituximab therapy, the recommended dose is 1000 mg administered intravenously on day 1 and day 15, or alternatively 375 mg/m² once weekly for 4 weeks. 1
Dosing Regimens
Two standard dosing regimens are used for rituximab in hypersensitivity pneumonitis:
For maintenance therapy in refractory cases, rituximab may be repeated as needed based on clinical response, typically every 24 weeks 1
Patient Selection and Considerations
Rituximab is primarily used as salvage therapy for refractory hypersensitivity pneumonitis that has not responded to standard immunosuppressive therapy 2
Before initiating rituximab therapy, obtain:
- Baseline immunoglobulin levels (IgG, IgM, IgA)
- Hepatitis B and C antibody screening
- Latent tuberculosis screening 1
Monitor complete blood count with differential at baseline and at 2-4 month intervals during treatment 1
Administration and Monitoring
Premedication is recommended to reduce infusion reactions:
- Antipyretic (e.g., acetaminophen)
- Antihistamine (e.g., diphenhydramine) 1
Monitor closely for infusion reactions, which occur in up to 77% of patients during the first infusion 1
Infusion reactions management:
- For Grade 1/2 reactions: Slow or temporarily stop the infusion and provide symptomatic treatment
- For Grade 3/4 reactions: Stop the infusion, provide aggressive symptomatic treatment, and consider permanent discontinuation 1
Safety Considerations
Common adverse effects include:
- Infusion-related reactions (fever, chills, rigors)
- Cytopenias
- Increased risk of infections 1
Serious adverse events to monitor:
- Progressive multifocal leukoencephalopathy (rare but serious)
- Hepatitis B reactivation
- Severe infections 1
Rituximab-induced lung injury is a rare but potentially serious complication that requires a high index of suspicion 3, 4
Efficacy in Hypersensitivity Pneumonitis
A retrospective study of 20 patients with chronic hypersensitivity pneumonitis showed:
- Stabilization of forced vital capacity (FVC) after 6 months of rituximab therapy
- Significant reduction in the rate of FVC decline compared to pre-treatment period
- Stable diffusion capacity (DLCO) with improvement in 63% of patients 5
Consider rituximab particularly for patients with:
Hypersensitivity to Rituximab
- For patients who develop hypersensitivity to rituximab:
- Desensitization protocols may allow continued treatment
- Skin testing may be performed but has limited predictive value for reactions
- Elevated tryptase levels during reactions suggest mast cell involvement 6