following a full submission assessed under the orphan medicine process:
polatuzumab vedotin (Polivy®) is accepted for restricted use within NHSScotland.
Indication Under Review: in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (R-CHP) for the treatment of adult patients with previously untreated diffuse large B-cell lymphoma (DLBCL).
SMC restriction: patients with an International Prognostic Index (IPI) score of 2 to 5
Polatuzumab vedotin, in combination with R-CHP, resulted in a statistically significant improvement in investigator-assessed progression-free survival compared with rituximab, cyclophosphamide, vincristine, doxorubicin and prednisone (R-CHOP).
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.
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Medicine details
- Medicine name:
- polatuzumab vedotin (Polivy)
- SMC ID:
- SMC2525
- Indication:
In combination with rituximab, cyclophosphamide, doxorubicin, and prednisone, is indicated for the treatment of adult patients with previously untreated diffuse large B-cell lymphoma (DLBCL).
- Pharmaceutical company
- Roche
- BNF chapter
- Malignant disease and immunosuppression
- Submission type
- Full
- Status
- Restricted
- Date advice published
- 12 June 2023