Pharmacology · Platinum compounds
Carboplatin !
A gentler cousin of cisplatin: the same DNA cross-links with far less kidney damage and vomiting, but more bone-marrow suppression.
Updated 2026-11-01
The figure shows the cisplatin adduct. Carboplatin leaves the same diammine-platinum on DNA after losing its cyclobutane-dicarboxylate group, so the lesion is equivalent.
Mechanism of action
Carboplatin carries a cyclobutane-dicarboxylate leaving group that is displaced more slowly than cisplatin's chlorides. Once activated it forms the same platinum–DNA cross-links as cisplatin and causes equivalent lesions. The slower activation makes it less toxic to the kidney, ear and nerves, while bone-marrow suppression becomes the main toxicity.
- Slow loss of the dicarboxylate leaving group
- Platinum binds guanine N7 like cisplatin
- DNA cross-links block replication
- Dividing cells die; marrow takes the main hit
Pharmacokinetics
- Absorption
- Intravenous only.
- Elimination
- Mainly by the kidneys, so exposure follows kidney function; the dose is calculated from the glomerular filtration rate (Calvert formula).
Indications
- Advanced ovarian carcinoma, first line in combination and for recurrence. Ovarian cancer →
Adverse effects
Common
- Myelosuppression: thrombocytopenia, neutropenia and cumulative anaemia
- Nausea and vomiting (milder than cisplatin)
- Low magnesium and other electrolytes
- Peripheral neuropathy, uncommon
Contraindications
- History of severe allergic reactions to cisplatin, other platinum compounds or mannitol
- Severe bone-marrow depression or significant bleeding
Key interactions
- Aminoglycosides
- More kidney and hearing toxicity.
- Other nephrotoxic drugs
- Carboplatin may add to their kidney effects.
- Other myelosuppressive therapy
- Additive marrow suppression; dose and timing are adjusted.
What is monitored
- Blood counts frequently, until recovery
- Kidney function (to calculate the dose) and electrolytes
- Allergic reactions during every infusion
Administration and safety
- Look-alike risk with cisplatin: the name is read in full and the dose is checked against kidney function.
- Never prepared or given with needles or sets that contain aluminium: aluminium makes it precipitate and lose potency.
- Emergency drugs for anaphylaxis are at hand during every infusion.
- Hazardous drug: prepared and given following hazardous-drug handling procedures (impervious gloves, no skin contact) and disposed of as cytotoxic waste.
Nursing care
- Independent double check of drug, patient, route and cycle before giving it (high-alert medicine).
- Blood count before each cycle; fever with neutropenia is treated as an emergency.
- Watch for flushing, rash, wheeze or low blood pressure during the infusion; stop and call for help if they appear.
- Bleeding precautions when platelets are low (soft toothbrush, no injections in the muscle).
- Teaching: report fever, chills, sore throat, bleeding or bruising at once.
Pregnancy and breastfeeding
May cause fetal harm (embryotoxic and teratogenic in animals); pregnancy is avoided during treatment.
Test yourself
Think of the answer, then tap the question to see it.
Compared with cisplatin, what is carboplatin's main dose-limiting toxicity?
Myelosuppression, especially thrombocytopenia; kidney damage and vomiting are milder.
Which patient value is used to calculate a carboplatin dose?
Kidney function (glomerular filtration rate), using the Calvert formula and a target AUC.
Minutes into a carboplatin infusion a patient develops flushing, wheeze and low blood pressure. What is the likely cause?
A platinum hypersensitivity (anaphylactic-like) reaction; the infusion is stopped and it is treated with epinephrine, corticosteroids and antihistamines.
Related drugs
Related conditions
← Back to the class: Platinum compounds
Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.
Sources: DailyMed - CARBOPLATIN injection, solution (DailyMed (U.S. National Library of Medicine), 2025); Goodman & Gilman's The Pharmacological Basis of Therapeutics, 14th ed., ch. 70 (McGraw Hill, 2023); ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026); eEML - Electronic Essential Medicines List (World Health Organization, 2025).
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Representative model, for educational purposes only.