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