Buy Thiotepa (Tepadina) online
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Known as original brand(s)
Tepadina
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Thiotepa is an ethylenimine-derived alkylating antineoplastic agent originally marketed under the brand name Tepadina. It is widely utilized in hematologic oncology as a component of conditioning regimens prior to hematopoietic stem cell transplantation (HSCT), as well as in the management of solid tumors.
The mechanism of action of thiotepa involves the formation of active ethylenimine radicals that cross-link DNA strands and disrupt nucleic acid synthesis. The drug alkylates guanine residues, inhibits DNA and RNA replication, and blocks cell division. Due to its high lipophilicity, thiotepa readily crosses the blood-brain barrier and penetrates the cerebrospinal fluid.
Clinical administration of thiotepa achieves profound myeloablation and immunosuppression before bone marrow transplantation and controls the progression of breast, ovarian, and bladder malignancies.
Indications
Thiotepa is indicated in oncology and hematology for the following applications:
- Conditioning for HSCT: Conditioning regimen prior to autologous or allogeneic hematopoietic stem cell transplantation in adult and pediatric patients with hematologic diseases or solid tumors.
- Breast and Ovarian Cancer: Palliative treatment of advanced adenocarcinoma of the breast and ovary.
- Bladder Cancer: Intravesical administration for the prevention of recurrence of superficial bladder papillary carcinoma following transurethral resection.
- Malignant Effusions: Intracavitary control of malignant pleural, pericardial, or peritoneal effusions.
Dosage and administration
Thiotepa is administered parenterally (intravenously, intracavitary, or intravesically) in a specialized hospital setting:
- Conditioning Regimens (HSCT): Dosing ranges from 5 mg/kg to 10 mg/kg (or 150 to 900 mg/m² body surface area) depending on the transplantation protocol.
- Systemic Chemotherapy: For solid tumors, standard doses range from 15 mg/m² to 30 mg/m² every 1 to 4 weeks (or 0.3 to 0.4 mg/kg).
- Intravesical Administration: Instillation of 30 mg to 60 mg diluted in 30 to 60 mL of sterile water retained in the bladder for 2 hours once weekly for 4 to 8 weeks.
- Administration Technique: Intravenous infusions are typically administered over 2 to 4 hours. Adequate hydration is required prior to high-dose therapy.
- Monitoring: Frequent monitoring of complete blood count (leukocytes, neutrophils, platelets) and renal/hepatic function is required.