Drug Guide
Pentostatin
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Purine analog Antimetabolite
FDA Approved Indications
- Hairy cell leukemia
Mechanism of Action
Pentostatin inhibits adenosine deaminase, leading to accumulation of deoxyadenosine triphosphate, which is toxic to lymphocytes, thus suppressing lymphocyte proliferation.
Dosage and Administration
Adult: 4 mg/m² IV every 2 weeks for up to 6 doses; dosage may vary based on response and tolerability.
Pediatric: Use not well established; consult specialist.
Geriatric: Dosage adjustments not usually required but monitor renal function closely.
Renal Impairment: Adjust dose based on renal function; consult specific guidelines.
Hepatic Impairment: Use with caution; no specific adjustment guidelines available.
Pharmacokinetics
Absorption: Not applicable (intravenous administration).
Distribution: Widely distributed; crosses blood-brain barrier.
Metabolism: Minimal metabolism; mainly excreted unchanged.
Excretion: Renally excreted; monitor renal function.
Half Life: Approximately 20 hours.
Contraindications
- Hypersensitivity to pentostatin or its components.
Precautions
- Use with caution in patients with renal impairment, as drug is renally excreted.
- Monitor blood counts regularly due to risk of myelosuppression.
- Use caution in patients with active infections or immunodeficiency.
Adverse Reactions - Common
- Myelosuppression (neutropenia, thrombocytopenia, anemia) (Common)
- Nausea, vomiting (Common)
- Rash, fever (Common)
Adverse Reactions - Serious
- Severe myelosuppression leading to infection or bleeding (Less common)
- Liver toxicity (Rare)
- Pulmonary toxicity (Rare)
- Secondary malignancies (Rare)
Drug-Drug Interactions
- Other myelosuppressive agents, immunosuppressants, nephrotoxic drugs.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor complete blood counts frequently, renal function, and signs of infection.
Diagnoses:
- Risk for infection related to myelosuppression
- Risk for bleeding due to thrombocytopenia
Implementation: Administer as scheduled, monitor blood counts, and observe for adverse effects.
Evaluation: Assess for hematologic response and adverse effects; adjust therapy accordingly.
Patient/Family Teaching
- Report signs of infection (fever, chills), bleeding, or severe fatigue immediately.
- Adhere to scheduled blood tests.
- Use caution to prevent injury due to bleeding risk.
Special Considerations
Black Box Warnings:
- Myelosuppression may be severe and life-threatening.
- Infection risk is increased.
- Secondary malignancies, including skin cancers, may occur.
Genetic Factors: N/A
Lab Test Interference: May cause anemia, leukopenia, thrombocytopenia, which requires careful interpretation of CBCs.
Overdose Management
Signs/Symptoms: Severe myelosuppression, infection, bleeding.
Treatment: Supportive care, blood product transfusions, antibiotics if infections develop, and monitoring in an intensive setting.
Storage and Handling
Storage: Store at room temperature, protected from light.
Stability: Stable for specified period as per manufacturer guidelines.