Drug Guide

Generic Name

Ziv-aflibercept

Brand Names Zaltrap

Classification

Therapeutic: Antineoplastic agent

Pharmacological: Vascular endothelial growth factor (VEGF) inhibitor

FDA Approved Indications

Mechanism of Action

Ziv-aflibercept is a recombinant fusion protein that acts as a decoy receptor for VEGF-A, VEGF-B, and placental growth factor (PLGF). By binding these ligands, it prevents them from activating their natural receptors on endothelial cells, thereby inhibiting angiogenesis required for tumor growth.

Dosage and Administration

Adult: 4 mg/kg IV every 2 weeks in combination with fluorouracil, leucovorin, and oxaliplatin (FOLFOX).

Pediatric: Not approved for pediatric use.

Geriatric: No specific dose adjustment, but caution advised due to potential increased risk of adverse effects.

Renal Impairment: No specific recommendations; use with caution.

Hepatic Impairment: No specific dose adjustments; monitor closely.

Pharmacokinetics

Absorption: Administered IV; absorption phase bypassed.

Distribution: Extensive distribution, high plasma protein binding.

Metabolism: Metabolized via proteolytic degradation.

Excretion: Excreted mainly unchanged in feces and urine.

Half Life: about 6 days.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

Drug-Herb Interactions

Nursing Implications

Assessment: Monitor blood pressure, renal function, urinalysis for proteinuria, wound healing status, signs of bleeding, ocular health.

Diagnoses:

  • Risk for bleeding, risk for hypertension, impaired skin integrity, knowledge deficit regarding therapy.

Implementation: Administer as prescribed, monitor for adverse effects, educate patient on signs to report, ensure proper infusion technique.

Evaluation: Outcome of blood pressure control, absence of bleeding complications, tumor response, patient understanding.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: No specific genetic testing required.

Lab Test Interference: May affect coagulation parameters and urinalysis results.

Overdose Management

Signs/Symptoms: Severe bleeding, hypertension, or signs of thromboembolism.

Treatment: Supportive care, maintain blood pressure, control bleeding, no specific antidote available.

Storage and Handling

Storage: Store refrigerated at 2°C to 8°C (36°F to 46°F), protect from light.

Stability: Stable refrigerated; vials should be used within the period specified by the manufacturer once reconstituted.

This guide is for educational purposes only and is not intended for clinical use.