[A24-100] Binimetinib and encorafenib (NSCLC) – Benefit assessment according to §35a Social Code Book V

Last updated 02.01.2025

Project no.:
A24-100

Commission:
Commission awarded on 26.09.2024 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Topic:
Cancer

Indication:

Adult patients with advanced non-small cell lung cancer with a rapidly accelerated fibrosarcoma isoform B V600E mutation

Result of dossier assessment:
  • Patients with PD-L1 expression ≥ 50%, first-line treatment: added benefit not proven.
  • Patients with PD-L1 expression < 50%, first-line treatment: added benefit not proven.
  • Patients after first-line treatment: added benefit not proven.
Note:

After completion of the assessment by IQWiG the Federal Joint Committee (G-BA) conducts a commenting procedure. This may provide supplementary information and as a result lead to a modified benefit assessment. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA website.

DOI:

https://doi.org/10.60584/A24-101

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