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The content on this page is not current guidance and is only for the purposes of the consultation process.

1 Recommendations

1.1 Tebentafusp is not recommended, within its marketing authorisation, for treating HLA-A*02:01-positive unresectable or metastatic uveal melanoma in adults.

1.2 This recommendation is not intended to affect treatment with tebentafusp that was started in the NHS before this guidance was published. People having treatment outside this recommendation may continue without change to the funding arrangements in place for them before this guidance was published, until they and their NHS clinician consider it appropriate to stop.

Why the committee made these recommendations

There is no standard treatment for HLA-A*02:01-positive advanced uveal melanoma. Usually people are offered immunotherapies licensed for treating cutaneous melanoma, such as pembrolizumab, or chemotherapy. Tebentafusp aims to treat the specific features of HLA-A*02:01-positive uveal melanoma.

Clinical trial evidence suggests that tebentafusp could increase how long people live and the length of time before their cancer gets worse compared with the usual treatments offered, but this is uncertain.

Tebentafusp meets the criteria for a life-extending treatment at the end of life. Because of the clinical uncertainty, the cost-effectiveness estimates are uncertain. They are also all higher than what NICE considers an acceptable use of NHS resources for end of life treatments. So, tebentafusp is not recommended.