Similarly, within KEYNOTE-407, pembrolizumab plus platinum/taxane demonstrated improved ORR (57.9% vs. 48%), PFS (HR 0.62, P<0.001) and OS (HR 0.78, P=0.02) for non-squamous NSCLC patients regardless of PD-L1 staining when compared to carboplatin plus paclitaxel plus bevacizumab ( 12). In IMpower150, the regimen of ABCP also demonstrated improved ORR (63.5% vs. 18.9%, P<0.001), PFS and OS (HR 0.49, P<0.001) than platinum/pemetrexed across non-squamous NSCLC patients with any level PD-L1 staining (including PD-L1 negative patients) ( 10). In KEYNOTE-189, pembrolizumab plus platinum/pemetrexed had better ORR (47.6% vs. For patients lacking EGFR activating mutations/ ALK fusions these chemo-immunotherapy combinations improved efficacy outcomes compared to platinum-based chemotherapy ( 10- 12). Following this, both atezolizumab plus bevacizumab plus carboplatin plus paclitaxel (ABCP) and pembrolizumab plus histology dependent chemotherapy were compared to platinum-based chemotherapy in randomized phase III trials. Subsequently, KEYNOTE-024 demonstrated that for advanced/metastatic NSCLC patients with PD-L1 ≥50% on TCs by the 22-C3 immunohistochemistry assay and lacking EGFR activating mutations/ ALK fusions that pembrolizumab had a significantly greater objective response rate (ORR), progression-free survival (PFS) and OS when compared to platinum-based doublets as first-line therapy ( 8, 9).īecause of KEYNOTE-024, multiple regulatory agencies and guideline panels approved pembrolizumab monotherapy for patients with newly diagnosed advanced/metastatic NSCLC, PD-L1 ≥50% on TCs and lacking EGFR activating mutations/ ALK fusions. In each of these second-line trials patients with epidermal growth factor receptor (EGFR) activating mutations did not benefit from PD-1 axis inhibitors when compared to docetaxel, with data on any included ALK rearranged patients not detailed ( 4- 7). Within KEYNOTE-010, patients with PD-L1 ≥50% on tumor cells (TCs) administered pembrolizumab had a greater magnitude of benefit compared to docetaxel than patients with PD-L1 of 1–49% ( 6). In each of these trials, there was an OS benefit when comparing the respective PD-1 or PD-L1 inhibitor to docetaxel ( 4- 7). ![]() ![]() Subsequently, randomized phase III trials comparing atezolizumab, nivolumab or pembrolizumab to docetaxel as second-line therapy were conducted in NSCLC. Prior to the advent of inhibitory antibodies targeting programmed death 1 (PD-1) or programmed death ligand 1 (PD-L1), the median overall survival (OS) for advanced/metastatic non-small cell lung cancer (NSCLC) patients receiving first-line platinum doublet chemotherapy was approximately 8–12 months and 5-year survival rates were estimated at 2% ( 1- 3). Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042): a randomised, open-label, controlled, phase 3 trial. Email: This is an invited article commissioned by the Section Editor Kaiping Zhang, PhD (AME College, AME Group, China).Ĭomment on: Mok TSK, Wu YL, Kudaba I, et al. Thoracic Oncology Program, Division of Medical Oncology, Department of Internal Medicine, University of Colorado Cancer Center, Aurora, CO, USA. ![]() Interviews with Outstanding Guest EditorsĬorrespondence to: Jose M.Policy of Dealing with Allegations of Research Misconduct.Policy of Screening for Plagiarism Process.
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