Evidence Level:Sensitive: A2 - Guideline
Title:
Therapy for Stage IV Non–Small-Cell Lung Cancer Without Driver Alterations: ASCO Living Guideline, Version 2023.1
Excerpt:For patients with SCC, PD-L1 TPS 0%-49% and PS 0-1, clinicians may offer cemiplimab plus chemotherapy…
Evidence Level:Sensitive: C1 - Off-label
(Approved for Non Small Cell Lung Cancer)
New
Title:
LIBTAYO® (CEMIPLIMAB) IN COMBINATION WITH CHEMOTHERAPY APPROVED BY EUROPEAN COMMISSION FOR THE FIRST-LINE TREATMENT OF ADVANCED PD-L1 POSITIVE NON-SMALL CELL LUNG CANCER (NSCLC)
Excerpt:Regeneron Pharmaceuticals...announced that the European Commission (EC) approved Libtayo® (cemiplimab) in combination with platinum-based chemotherapy for the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) with ≥1% PD-L1 expression. This includes patients that have no EGFR, ALK or ROS1 aberrations and whose tumors are metastatic or locally advanced and not candidates for definitive chemoradiation.
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
Combinations of Cemiplimab (Anti-PD-1 Antibody) and Platinum-based Doublet Chemotherapy in Patients With Lung Cancer
Excerpt:...Part 1 only: Expression of PD-L1 in ...
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
REGN2810 (Anti-PD-1 Antibody), Platinum-based Doublet Chemotherapy, and Ipilimumab (Anti-CTLA-4 Antibody) Versus Pembrolizumab Monotherapy in Patients With Lung Cancer
Excerpt:...Expression of PD-L1 in ≥50% of tumor cells determined by the commercially available assay performed by the central laboratory 4....
More C2 evidence
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
A Study of REGN2810 and Ipilimumab in Patients With Lung Cancer
Excerpt:...Biopsy evaluable for expression of PD-L1 as determined by a PD-L1 Immunohistochemistry (IHC) pharma diagnostic test (pharmDx) assay performed by a central laboratory 4....