
Carboplat10 mg/ml
Beacon Pharmaceuticals PLC
Carboplatin is a platinum-based chemotherapy agent used in the treatment of certain cancers, primarily as part of physician-supervised combination or single-agent regimens.
Carboplatin is a platinum-based chemotherapy agent used in the treatment of certain cancers, primarily as part of physician-supervised combination or single-agent regimens.
Carboplatin is widely used, based on strong clinical evidence and inclusion in oncology treatment guidelines, in combination regimens (often with a taxane such as paclitaxel) for:
These non-ovarian uses are considered off-label relative to the original approved labeling but are standard of care in many oncology guidelines and must only be prescribed by an oncologist.
Carboplatin must be administered by intravenous infusion, under the supervision of a physician experienced in cancer chemotherapy. Dosing is highly individualized and commonly calculated using the Calvert formula, based on the patient's renal function (glomerular filtration rate, GFR) and a target area-under-curve (AUC):
Total Dose (mg) = Target AUC (mg/mL·min) × (GFR + 25)
| Indication / Regimen | Typical Adult Dosing |
|---|---|
| Single-agent therapy (previously untreated) | 360 mg/m² IV once every 4 weeks, or AUC-based dosing (target AUC typically 5-7 mg/mL·min) |
| Combination therapy with cyclophosphamide (advanced ovarian carcinoma) | 300 mg/m² IV once every 4 weeks for 6 cycles, in combination with cyclophosphamide 600 mg/m² |
| Combination regimens (e.g., with paclitaxel, for various solid tumors, off-label) | AUC 5-6 mg/mL·min IV once every 3-4 weeks, per specific oncology protocol |
| Platelet count | Neutrophil count | Dose adjustment |
|---|---|---|
| >100,000/mm³ | >2,000/mm³ | 125% of prior course dose |
| 50,000-100,000/mm³ | 500-2,000/mm³ | No adjustment (100% of prior dose) |
| <50,000/mm³ | <500/mm³ | 75% of prior course dose |
Renal function markedly affects Carboplatin clearance; the Calvert formula inherently adjusts for this, but general starting-dose guidance for single-agent use in adults with reduced renal function has included creatinine clearance 41-59 mL/min: approximately 250 mg/m² IV; creatinine clearance 16-40 mL/min: approximately 200 mg/m² IV. Patients with creatinine clearance below 15 mL/min are not well studied; use requires extreme caution and specialist oncology/nephrology input.
Carboplatin is administered only as a slow intravenous infusion, typically over 15-60 minutes, after dilution in 5% dextrose or 0.9% sodium chloride. Do not use needles or IV administration sets containing aluminum parts, as aluminum reacts with Carboplatin causing precipitate formation and loss of potency. Antiemetic premedication is standard practice before administration, as Carboplatin is highly emetogenic. Only healthcare professionals trained in handling cytotoxic drugs should prepare and administer Carboplatin.
See Pediatric Use and Use in Special Populations for further detail.
Carboplatin commonly causes dose-related adverse effects, most notably on the bone marrow and gastrointestinal system.
Carboplatin is contraindicated in patients with:
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