Drug Guide
Thiotepa
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Alkylating agent
FDA Approved Indications
- Intravesical chemotherapy for bladder cancer
- Preparation for bone marrow transplant in hematologic malignancies
Mechanism of Action
Thiotepa is an alkylating agent that crosslinks DNA strands, inhibiting DNA replication and leading to cell death, primarily affecting rapidly dividing cells.
Dosage and Administration
Adult: Dose varies based on treatment protocol, generally given intravenously or intravesically as per oncologist instructions.
Pediatric: Used with caution; dose determined by body surface area and treatment protocol.
Geriatric: Adjusted based on renal and hepatic function, with careful monitoring.
Renal Impairment: Dose adjustment may be necessary due to decreased clearance.
Hepatic Impairment: Use with caution; monitor liver function due to potential hepatotoxicity.
Pharmacokinetics
Absorption: Rapid when administered intravenously.
Distribution: Widely distributed in body tissues, crossing the blood-brain barrier.
Metabolism: Extensively metabolized in the liver.
Excretion: Primarily excreted via urine.
Half Life: Approximately 3-4 hours.
Contraindications
- Hypersensitivity to thiotepa or other alkylating agents.
- Severe myelosuppression.
Precautions
- Use cautiously in hepatic or renal impairment.
- Pregnancy Category D: risk to fetus; effective contraception recommended during treatment and for some time after.
Adverse Reactions - Common
- Bone marrow suppression (neutropenia, thrombocytopenia, anemia) (Common)
- Alopecia (Common)
- Nausea and vomiting (Common)
Adverse Reactions - Serious
- Hemorrhagic cystitis (Serious)
- Secondary malignancies (late effect) (Rare)
- Severe infections due to immunosuppression (Serious)
Drug-Drug Interactions
- Other myelosuppressive agents, including radiation therapy
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood counts regularly; assess renal and hepatic function.
Diagnoses:
- Risk for infection
- Impaired tissue integrity
- Risk for bleeding
Implementation: Administer as ordered; implement protective precautions against infection; monitor for signs of hemorrhagic cystitis.
Evaluation: Assess blood counts; monitor for adverse effects; evaluate response to treatment.
Patient/Family Teaching
- Report symptoms of infection, bleeding, or unusual fatigue.
- Maintain hydration to prevent cystitis.
- Follow instructions regarding contraception.
- Avoid contact with sick individuals.
Special Considerations
Black Box Warnings:
- May cause severe myelosuppression leading to infection, bleeding, and anemia.
- Potential for secondary malignancies.
Genetic Factors: Not well characterized; genetic variations may affect metabolism and toxicity.
Lab Test Interference: May cause false elevation of serum creatinine.
Overdose Management
Signs/Symptoms: Bone marrow suppression, hemorrhagic cystitis, severe mucositis.
Treatment: Supportive care, discontinuation of drug, and possibly administration of hematopoietic growth factors or transfusions.
Storage and Handling
Storage: Store at room temperature, protected from light.
Stability: Stable under recommended storage conditions for the duration of shelf life.