Patient group a1
Patientinnen mit primär fortgeschrittener Erkrankung
Neues Anwendungsgebiet: primär fortgeschrittenes oder rezidiviertes Endometriumkarzinom mit dMMR/ MSI-H, Kombination mit Carboplatin und Paclitaxel
G-BA action
final resolution
2024-06-20
Evidence-checked summary
The G-BA found no proven added benefit for Patientinnen mit primär fortgeschrittener Erkrankung. The appropriate comparator was - Carboplatin + Paclitaxel. The G-BA found an indication of major added benefit for Patientinnen mit rezidivierender Erkrankung. The appropriate comparator was - Carboplatin + Paclitaxel. The G-BA issued a final resolution on 2024-06-20. The official page states that it took effect as follows: 20.06.2024. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.
This is the latest validated public action attached to this case. It is separate from the IQWiG assessment result.
Final benefit result
Patient group a1
Patientinnen mit primär fortgeschrittener Erkrankung
Patient group a2
Patientinnen mit rezidivierender Erkrankung
Official case record
No inferred stages
Consultation record
2024-05-06
65 parsed turns
Oral hearing: Dostarlimab (Neues Anwendungsgebiet: primär fortgeschrittenes oder rezidiviertes Endometriumkarzinom mit dMMR/ MSI-H, Kombination mit Carboplatin und Paclitaxel)
Official Wortprotokoll · 11 pages
IQWiG comparison
IQWiG assessment findings and the later G-BA action are separate records. Open both to compare them.
A23-143
matched
Dostarlimab (endometrial cancer) – Benefit assessment according to §35a Social Code Book V
Official assessment PDF · 139 pages
G-BA decisions
2024-06-20
final resolution
The G-BA found no proven added benefit for Patientinnen mit primär fortgeschrittener Erkrankung. The appropriate comparator was - Carboplatin + Paclitaxel. The G-BA found an indication of major added benefit for Patientinnen mit rezidivierender Erkrankung. The appropriate comparator was - Carboplatin + Paclitaxel. The G-BA issued a final resolution on 2024-06-20. The official page states that it took effect as follows: 20.06.2024. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.
3 official documents · 5 cited claims
Official sources