Drug Guide
Loncastuximab Tesirine-lpyl
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Antibody-drug conjugate
FDA Approved Indications
- Relapsed or refractory large B-cell lymphoma (including diffuse large B-cell lymphoma, high-grade B-cell lymphoma, and transformed follicular lymphoma)
Mechanism of Action
Loncastuximab tesirine-lpyl is an antibody-drug conjugate that targets CD19-positive B cells. It binds to CD19 on B cells and delivers a cytotoxic agent, tesirine, which induces cell death.
Dosage and Administration
Adult: Overall, the recommended dosage is 0.15 mg/kg intravenously on Days 1-2 of a 21-day cycle. The dose may be repeated every 3 weeks.
Pediatric: Not approved for pediatric use.
Geriatric: No specific dosage adjustment; consider age-related factors.
Renal Impairment: No specific adjustment recommended.
Hepatic Impairment: No specific adjustment recommended.
Pharmacokinetics
Absorption: Rapid subcutaneous absorption; intravenous administration provides immediate bioavailability.
Distribution: Extensive in plasma and tissues.
Metabolism: Metabolized through lysosomal degradation of the antibody and release of the cytotoxic payload.
Excretion: Not fully characterized; likely via proteolytic degradation pathways.
Half Life: Approximately 4 days.
Contraindications
- Hypersensitivity to loncastuximab tesirine-lpyl or its components.
Precautions
- Monitor for infusion-related reactions, hepatotoxicity, myelosuppression. Use with caution in patients with active infections or comorbidities that could impair immune response.
Adverse Reactions - Common
- Thrombocytopenia (Common)
- Neutropenia (Common)
- Elevated liver enzymes (Common)
- Infusion-related reactions (Common)
Adverse Reactions - Serious
- Severe thrombocytopenia leading to bleeding (Serious)
- Severe neutropenia leading to infections (Serious)
- Serious infections including pneumonia, sepsis (Serious)
- Hepatotoxicity including hepatitis, elevated bilirubin (Serious)
Drug-Drug Interactions
- Caution with other myelosuppressive agents, immunosuppressants, or therapies impacting hepatic function.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood counts, liver function tests, and for symptoms of infection or infusion reactions.
Diagnoses:
- Risk for bleeding, Risk for infection, Impaired tissue integrity.
Implementation: Administer as scheduled, premedicate for infusion reactions if necessary, monitor patient closely during and after infusion.
Evaluation: Assess for response to therapy, side effects, and adverse reactions; adjust treatment as necessary.
Patient/Family Teaching
- Report signs of infection, unusual bleeding, or infusion reactions immediately.
- Maintain good hygiene and infection control measures.
- Follow-up appointments for blood tests and monitoring.
Special Considerations
Black Box Warnings:
- Serious infections, hepatotoxicity, and embryo-fetal toxicity.
Genetic Factors: No specific genetic considerations reported.
Lab Test Interference: Can cause increases in serum liver enzymes, which should be interpreted carefully.
Overdose Management
Signs/Symptoms: Severe cytopenias, hepatotoxicity, infusion reactions.
Treatment: Supportive care, including transfusions, corticosteroids, antibiotics, and symptomatic management; no specific antidote.
Storage and Handling
Storage: Store at 2°C to 8°C (36°F to 46°F). Protect from light.
Stability: Stable up to the expiration date when stored properly.