
Cisplat1 mg/ml
Healthcare Pharmaceuticals Ltd.
Established / FDA-Approved Uses Metastatic testicular tumors : Cisplatin is indicated, in established combination chemotherapy regimens with other cytotoxic agents and more.
Cisplatin is a highly toxic cytotoxic chemotherapy medicine and must only be prescribed, dispensed, and administered under the close supervision of a qualified oncologist experienced in the use of cancer chemotherapeutic agents, with adequate facilities for monitoring and managing toxicity.
Cisplatin dosing is individualized by the treating oncologist based on indication, body surface area, prior treatment, and organ function, and is always given as an intravenous infusion with mandatory pre- and post-hydration. Representative regimens described in oncology references include:
| Indication | Typical Dose | Schedule |
|---|---|---|
| Metastatic testicular tumors (combination) | 20 mg/m² IV | Once daily for 5 consecutive days, repeated every 3 weeks for 3 cycles or more, per protocol |
| Metastatic ovarian tumors (with cyclophosphamide) | 75–100 mg/m² IV | Once every 4 weeks |
| Metastatic ovarian tumors (single agent) | 100 mg/m² IV | Once every 4 weeks |
| Advanced bladder cancer (single agent) | 50–70 mg/m² IV | Once every 3–4 weeks (lower end of range, or more frequent lower doses, in previously irradiated or heavily pretreated patients) |
Doses greater than 100 mg/m² per cycle every 3 to 4 weeks are rarely used because of increasing toxicity without a clear added benefit.
To reduce nephrotoxicity, patients must receive vigorous pre-treatment hydration, typically 1 to 2 liters of intravenous fluid infused over 8 to 12 hours before each dose of Cisplatin. Cisplatin is then administered as an infusion, commonly diluted in dextrose/saline solution with mannitol, over 6 to 8 hours (or per institutional protocol), followed by adequate post-hydration and maintained urine output (generally at least 100 mL/hour) for several hours after the infusion. Adequate hydration and, when required, forced diuresis must be ensured before proceeding with each cycle.
Renal function (serum creatinine, BUN, creatinine clearance) and electrolytes must be assessed before the first dose and before each subsequent course; Cisplatin should not be re-administered until renal function has returned to acceptable levels, and dose reduction or delay is required for renal impairment (see Contraindications for pre-existing significant renal impairment).
No well-established dedicated dose-adjustment guidelines exist for hepatic impairment; use with caution and close monitoring, as directed by the treating oncologist.
Dose modification, delay, or discontinuation may be required for significant myelosuppression, ototoxicity, neurotoxicity, or hypersensitivity reactions, at the discretion of the treating oncologist. Cisplatin must be taken/administered exactly as prescribed; do not alter the schedule, dose, or combination regimen without your oncologist's advice.
Patients should seek prompt medical attention for fever, signs of infection, unusual bleeding or bruising, severe or persistent vomiting, ringing in the ears, reduced urination, numbness/tingling, or any signs of an allergic reaction during or shortly after a Cisplatin infusion.
Note: renal impairment, myelosuppression, and hearing impairment are well-established absolute contraindications specific to Cisplatin's labeling due to its predictable, dose-related toxicity in these organ systems; less severe or borderline organ dysfunction still requires careful specialist risk-benefit assessment rather than automatic exclusion. See Precautions and Warnings for monitoring requirements during treatment.
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