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Platinum Chemotherapy — Head and Neck Cancer

Cisplatin

Brand names: Cisplatin Accord, Cisplatin Teva

Cisplatin is an intravenous platinum-based cytotoxic used, often with radiotherapy, in the treatment of head and neck squamous cell carcinoma and other solid tumours.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It forms platinum-DNA cross-links that disrupt DNA replication and transcription, triggering apoptosis of dividing tumour cells.

Prescribing in practice

  • Cisplatin is markedly nephrotoxic and ototoxic, and adequate intravenous hydration (with attention to electrolytes) is mandatory to limit renal damage, while baseline and ongoing assessment of renal function and hearing is required.
  • It is intensely emetogenic and requires guideline-based antiemetic prophylaxis, and it causes cumulative peripheral neuropathy and myelosuppression.
  • It is given under specialist oncology supervision with electrolyte monitoring, as hypomagnesaemia and other disturbances are common.

Monitoring

Monitor renal function, full blood count, electrolytes (including magnesium) and hearing, and assess for neuropathy before and during treatment.

Counselling the patient

  • Report new ringing in the ears or hearing changes promptly.
  • Nausea and tingling in the hands or feet should be reported to the team.
  • Plenty of fluids and blood tests are part of treatment to protect the kidneys.

Evidence & guidelines

Concurrent cisplatin-based chemoradiotherapy is a standard-of-care option for locally advanced head and neck cancer in oncology guidelines.

Reference: RTOG 0129; EXTREME Trial (Vermorken et al. NEJM 2008); NICE Guidance Head and Neck Cancer; SPC Cisplatin; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.