[A23-46] Lutetium vipivotide tetraxetan (prostate cancer) – Addendum to Commission A23-01

Last updated 06.07.2023

Project no.:
A23-46

Commission:
Commission awarded on 25.05.2023 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Cancer

Indication:

In combination with androgen deprivation therapy with or without androgen receptor pathway inhibition for the treatment of adult patients with progressive prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer who have been treated with androgen receptor pathway inhibition and taxane-based chemotherapy

Result of dossier assessment:
  • Patients for whom abiraterone in combination with prednisone or prednisolone, enzalutamide or best supportive care is the most appropriate therapy for the individual patient: after addendum now indication of major added benefit
  • Patients for whom cabazitaxel or olaparib is the most appropriate therapy for the individual patient: added benefit not proven
Note:

If the need for additional work on a project commissioned by the G-BA arises during consultations, then IQWiG presents a report in the form of an "addendum". The G-BA subsequently decides on the extent of the added benefit, thus completing the early benefit assessment.

Federal Joint Committee (G-BA)

2023-07-06 A G-BA decision was published.

G-BA documents on this decision

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