Nivolumab for treating resectable (tumours ≥4 cm or node positive) non-small-cell lung cancer
5 October 2026
Condition
Cancer
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Published on 05 Oct 2026
Last Updated on 05 Oct 2026
Guidance Recommendations
The Ministry of Health’s Drug Advisory Committee has recommended:
Nivolumab 40 mg/4 mL, 100 mg/10 mL and 240 mg/24 mL concentrate for solution for infusion when used in combination with platinum-doublet chemotherapy for neoadjuvant treatment of resectable (tumours ≥4 cm or node positive) non-small-cell lung cancer. Maximum treatment duration: 3 cycles.
The decision was based on acceptable clinical effectiveness and pricing proposal by the company.
Funding Status
Nivolumab 40 mg/4 mL, 100 mg/10 mL and 240 mg/24 mL concentrate for solution for infusion are recommended for inclusion on the Medication Assistance Fund (MAF) for the abovementioned indication from 1 December 2026.
Clinical indication, subsidy class and MediShield Life claims eligibility for nivolumab are provided in the Annex.
