KEYTRUDA (pembrolizumab) - Renal cell carcinoma (RCC)
Reason for request
Key points
Favourable opinion for reimbursement of KEYTRUDA in combination with lenvatinib for the first-line treatment of adult patients with advanced clear-cell renal cell carcinoma only.
Unfavourable opinion for reimbursement of KEYTRUDA in combination with lenvatinib in the other situations covered by the MA indication.
Clinical Benefit
Substantial |
The Committee deems that the clinical benefit of KEYTRUDA 25 mg/ml (pembrolizumab) in combination with lenvatinib is substantial in the first-line treatment of advanced renal cell carcinoma, only in clear-cell RCC or with a clear-cell component;
|
Insufficient |
The Committee deems that the clinical benefit of KEYTRUDA 25 mg/ml (pembrolizumab) in combination with lenvatinib is insufficient to justify public funding in the first-line treatment of advanced renal cell carcinoma with a histological type other than clear-cell given the absence of robust data. |
Clinical Added Value
moderate |
Considering:
despite:
the Transparency Committee considers that the KEYTRUDA (pembrolizumab) + lenvatinib combination, like the pembrolizumab/axitinib combination and the nivolumab/cabozantinib combination, provides a moderate clinical added value (CAV III) compared to sunitinib in the first-line treatment of advanced clear-cell renal cell carcinoma or with a clear-cell component. |
Not applicable |