[A24-126] Tislelizumab (squamous NSCLC, first line) – Benefit assessment according to §35a Social Code Book (SGB) V

Last updated 01.04.2025

Project no.:
A24-126

Commission:
Commission awarded on 20.12.2024 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Topic:
Cancer

Indication:

First-line treatment of adult patients with squamous non-small cell lung cancer (NSCLC) with locally advanced NSCLC for whom surgical resection or platinum-based chemoradiation is not an option, or with metastatic NSCLC

Result of dossier assessment:
  • Patients with PD‑L1‑expression ≥ 50% and without treatable genetic alterations: added benefit not proven
  • Patients with PD‑L1‑expression < 50% and without treatable genetic alterations: 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/A24-126

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