Monograph Details

Neoplasms > Alkylating agents
THIOTEPA
Manufacturer
Various generic manufacturers
Legal Classification
Rx
Pharmacological Class
Alkylating agent.
Generic Name
Thiotepa 15mg, 30mg; per vial; pwd for IV, intravesical, or intracavitary administration after reconstitution.
Indications
Superficial papillary carcinoma of the urinary bladder. Adenocarcinomas of the breast and ovary. Intracavitary effusion due to neoplasm of serosal cavities.
Children
Not recommended.
Adults
Bladder cancer: avoid fluids 8–12 hrs prior to treatment. 60mg once weekly for 4 weeks; may repeat up to a total of 3 courses. Retain in bladder for 2 hours. IV administration: 0.3–0.4mg/kg IV once every 1–4 weeks. Intracavitary administration: 0.6–0.8mg/kg through same tube used to remove fluid from cavity.
Contraindications
Renal, hepatic, or bone marrow dysfunction; if need outweighs risk, may may be attempt a lower dose with close monitoring.
Precautions
Monitor blood and platelets weekly during and for at least 3 weeks after therapy. Discontinue if WBC ≤3000/mm3 or platelets ≤150,000/mm3. Use effective contraception if patient or partner is of childbearing potential. Elderly. Pregnancy (Cat.D). Nursing mothers: not recommended.
Interactions
Increased toxicity with concomitant or sequential alkylating agents (nitrogen mustards, cyclosphosphamide), radiation, myelosuppressants. Prolonged apnea with succinylcholine.
Adverse Reactions
Myelosuppresion, fatigue, febrile or allergic reactions, inj site reactions, urinary retention, dysuria, GI disturbances, anorexia, alopecia, dizziness, drowsiness, blurred vision, amenorrhea, interferes with spermatogenesis. Intravesical administration: systemic effects: rarely: chemical or hemorrhagic cystitis.
How Supplied
Contact supplier.
Additional Resources
Related Prescribing Note