Advice

following a full submission under the orphan equivalent medicine process:

brentuximab vedotin (Adcetris®) is accepted for use within NHSScotland.

Indication under review: for adult patients with previously untreated CD30+ Stage III or IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine and dacarbazine (AVD).

In an open-label, phase III study, six cycles of brentuximab vedotin (in combination with AVD) compared with six cycles of ABVD (doxorubicin, bleomycin, vinblastine and dacarbazine), significantly improved modified progression-free survival in adults with previously untreated CD30+ Stage III or IV HL.

This advice applies only in the context of an approved NHSScotland Patient Access Scheme (PAS) arrangement delivering the cost-effectiveness results upon which the decision was based, or a PAS/ list price that is equivalent or lower.

This advice takes account of the views from a Patient and Clinician Engagement (PACE) meeting.

Medicine details

Medicine name:
brentuximab vedotin (Adcetris)
SMC ID:
SMC2762
Indication:

Treatment of adult patients with previously untreated cell membrane receptor 30-positive (CD30+) Stage III or IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine and dacarbazine (AVD).

Pharmaceutical company
Takeda UK Ltd
BNF chapter
Malignant disease and immunosuppression
Submission type
Full
Status
Accepted
Date advice published
11 August 2025