Drug Guide
Siltuximab
Classification
Therapeutic: Antineoplastic, Immunosuppressant
Pharmacological: Chimeric Monoclonal Antibody
FDA Approved Indications
- Castleman's Disease (multicentric, HIV-negative, HHV-8-negative)
Mechanism of Action
Siltuximab binds to interleukin-6 (IL-6), preventing IL-6 from interacting with its receptor, thereby reducing inflammatory responses and tumor growth associated with cytokine-driven diseases.
Dosage and Administration
Adult: At presentation, 11 mg/kg IV every 3 weeks. Dose adjustments are not typically required. Pre-medication with antihistamines and corticosteroids is recommended to reduce infusion-related reactions.
Pediatric: Not approved for pediatric use; safety and efficacy not established.
Geriatric: No specific dosage adjustments required based on age.
Renal Impairment: No specific data; use with caution and monitor closely.
Hepatic Impairment: No specific data; use with caution, considering liver function tests.
Pharmacokinetics
Absorption: Administered IV; absorption not applicable.
Distribution: Distributed mainly in the vascular and extravascular compartments.
Metabolism: Metabolized via proteolytic pathways like other monoclonal antibodies.
Excretion: Primarily degraded into peptides and amino acids; not excreted renally.
Half Life: Approximately 16-18 days.
Contraindications
- Hypersensitivity to siltuximab or other components.
Precautions
- Monitor for infusion reactions, cytopenias, infections, and gastrointestinal perforation. Use caution in patients with active infections or immunosuppression.
Adverse Reactions - Common
- Infections (e.g., upper respiratory, urinary tract) (Common)
- Infusion reactions (fever, chills, rash) (Common)
- Fatigue, nausea, headache (Common)
Adverse Reactions - Serious
- Serious infections including sepsis (Less common)
- Gastrointestinal perforation (Rare)
- Hypersensitivity reactions (Rare)
Drug-Drug Interactions
- No significant direct interactions reported; caution when used with other immunosuppressants.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for infusion reactions, signs of infection, blood counts, liver function tests.
Diagnoses:
- Risk for infection
- Knowledge deficit related to drug therapy
Implementation: Administer infusion over 60 minutes; premedicate to reduce reactions. Regularly monitor blood counts and vital signs.
Evaluation: Assess patient for adverse effects and effectiveness of symptom control.
Patient/Family Teaching
- Report any signs of infection immediately.
- Inform about possible infusion reactions.
- Discuss importance of adhering to scheduled treatments and monitoring.
- Advise on warning signs such as fever, rash, or difficulty breathing.
Special Considerations
Black Box Warnings:
- Serious infections, including sepsis, can be life-threatening.
- Gastrointestinal perforation has been reported.
Genetic Factors: No specific genetic testing required.
Lab Test Interference: None documented.
Overdose Management
Signs/Symptoms: Potential for immune-related adverse effects, severe infusion reactions, or infections.
Treatment: Supportive care, discontinuation of drug, and symptomatic treatment as needed.
Storage and Handling
Storage: Store refrigerated at 2-8°C (36-46°F). Protect from light.
Stability: Product stability and expiry date provided on the packaging.