Icon of the Instituts for Quality and Efficiency in Health Care

[A22-70] Pembrolizumab (cervical cancer) – Benefit assessment according to § 35a SGB V

Last updated 02.02.2023

Project no.:
A22-70

Commission:
Commission awarded on 19.07.2022 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Cancer

Indication:

Adult patients with persistent, recurrent, or metastatic cervical cancer whose tumours express PD-L1 with a CPS ≥ 1

Result of dossier assessment:
  • First-line patients for whom cisplatin or carboplatin + paclitaxel ± bevacizumab is a suitable therapy of physician’s choice: hint of major added benefit
  • First-line patients for whom cisplatin or carboplatin + paclitaxel ± bevacizumab is no suitable therapy of physician’s choice: added benefit not proven
  • Patients after first-line chemotherapy and for whom further antineoplastic therapy is an option: 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.

Project no. Title Status
A22-72 Pembrolizumab (melanoma, adjuvant) – Benefit assessment according to § 35a SGB V Commission completed
A22-73 Pembrolizumab (melanoma, advanced) – Benefit assessment according to § 35a SGB V Commission completed
A22-36 Pembrolizumab (breast cancer, triple-negative, locally recurrent/metastatic, in combination with chemotherapy) – Addendum to Commission A21-145 Commission completed
A21-35 Pembrolizumab (Hodgkin lymphoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A21-34 Pembrolizumab (urothelial carcinoma first line treatment) - Benefit assessment according to §35a Social Code Book V (expiry of the decision) Commission completed
A21-163 Pembrolizumab (renal cell carcinoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A21-145 Pembrolizumab (breast cancer, triple-negative, locally recurrent/metastatic, in combination with chemotherapy) - Benefit assessment according to §35a Social Code Book V Commission completed
A21-144 Pembrolizumab (oesophageal cancer) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-99 Pembrolizumab (combination with axitinib, renal cell carcinoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-31 Pembrolizumab (squamous non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-30 Pembrolizumab (non-squamous non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-29 Pembrolizumab (melanoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-101 Pembrolizumab (head and neck squamous cell carcinoma, combination therapy) - Benefit assessment according to §35a Social Code Book V Commission completed
A19-100 Pembrolizumab (head and neck squamous cell carcinoma, monotherapy) - Benefit assessment according to §35a Social Code Book V Commission completed
A18-89 Pembrolizumab (urothelial carcinoma, first line) - Benefit assessment according to §35a Social Code Book V (new scientific findings) Commission completed
A18-67 Pembrolizumab (head and neck squamous cell carcinoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A17-46 Pembrolizumab (urothelial carcinoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A17-23 Pembrolizumab (classical Hodgkin lymphoma) - Benefit assessment according to §35a Social Code Book V Commission completed
A17-06 Pembrolizumab (non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V Commission completed
A16-55 Pembrolizumab (non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V Commission completed
A15-33 Pembrolizumab - Benefit assessment according to §35a Social Code Book V (dossier assessment) Commission completed
A22-71 Pembrolizumab (renal cell carcinoma) – Benefit assessment according to § 35a SGB V Commission completed
A22-79 Pembrolizumab (bile cancer) – Benefit assessment according to § 35a SGB V Commission completed
A22-78 Pembrolizumab (small bowel cancer) – Benefit assessment according to §35a Social Code Book V Commission completed
A22-77 Pembrolizumab (gastric cancer) – Benefit assessment according to §35a Social Code Book V Commission completed
A22-76 Pembrolizumab (endometrial cancer) – Benefit assessment according to §35a Social Code Book V Commission completed
A22-75 Pembrolizumab (colorectal cancer) – Benefit assessment according to § 35a SGB V Commission completed
A22-135 Pembrolizumab (cervical cancer) – Addendum to Commission A22-70 Commission completed
A24-46 Pembrolizumab (NSCLC, neoadjuvant + adjuvant) – Benefit assessment according to § 35a Social Code Book V Commission completed
A24-03 Pembrolizumab (biliary cancer) – Benefit assessment according to §35a Social Code Book V Commission completed
A24-47 Pembrolizumab (NSCLC, adjuvant) – Benefit assessment according to § 35a Social Code Book V Commission completed
A24-02 Pembrolizumab (gastric cancer, HER2-negative) – Benefit assessment according to §35a Social Code Book V Commission completed
A24-01 Pembrolizumab (gastric or gastro-oesophageal junction adenocarcinoma, HER2-positive) – Benefit assessment according to §35a Social Code Book V Commission completed

Federal Joint Committee (G-BA)

2023-02-02 A G-BA decision was published.

G-BA documents on this decision

Contact

Press contact

+49 221 356850

presse@iqwig.de

Info Service (German)

Subscribe to daily updated information on projects, calls for tender, current vacancies and events as well as our press releases.

Register

Contact form

Questions about commissions, publications and press releases can be sent to us via this form.

Contact form

Print page