Background The phase 3 JAVELIN Renal 101 trial (NCT02684006) demonstrated significantly improved progression-free survival (PFS) with first-line avelumab plus axitinib versus sunitinib in advanced renal cell carcinoma (aRCC). We report updated efficacy data from the second interim analysis.Patients and methods Treatment-naive patients with aRCC were randomized (1 : 1) to receive avelumab (10 mg/kg) intravenously every 2 weeks plus axitinib (5 mg) orally twice daily or sunitinib (50 mg) orally once daily for 4 weeks (6-week cycle). The two independent primary end points were PFS and overall survival (OS) among patients with programmed death ligand 1-positive (PD-L1+) tumors. Key secondary end points were OS and PFS in the overall population....
Abstract Although combination immune checkpoint inhibitor (immuno‐oncology [IO]) therapy is the firs...
PURPOSE: To evaluate the association between neutrophil-to-lymphocyte ratio (NLR) and efficacy of av...
Purpose To report updated analyses of the phase III CheckMate 214 trial with extended minimum follow...
BACKGROUND: The phase 3 JAVELIN Renal 101 trial (NCT02684006) demonstrated significantly improved...
BACKGROUND: Progression-free survival was significantly longer in patients who received avelumab plu...
BACKGROUND: Progression-free survival was significantly longer in patients who received avelumab plu...
Introduction. Simultaneous inhibition of programmed cell death-1 (PD-1)/PD-L1 immune checkpoint and ...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
BACKGROUND: Among patients with advanced renal cell carcinoma (RCC), those with sarcomatoid histolog...
BACKGROUND: Antibodies targeting programmed death-1 (PD-1) or programmed death-ligand 1 (PD-L1) have...
The randomized, open-label, phase 3 KEYNOTE-426 study (NCT02853331) demonstrated that pembrolizumab ...
BACKGROUND: In a single-group, phase 1b trial, avelumab plus axitinib resulted in objective respo...
BACKGROUND: In the phase 3 METEOR trial, cabozantinib improved progression-free survival (PFS), obje...
Abstract Although combination immune checkpoint inhibitor (immuno‐oncology [IO]) therapy is the firs...
PURPOSE: To evaluate the association between neutrophil-to-lymphocyte ratio (NLR) and efficacy of av...
Purpose To report updated analyses of the phase III CheckMate 214 trial with extended minimum follow...
BACKGROUND: The phase 3 JAVELIN Renal 101 trial (NCT02684006) demonstrated significantly improved...
BACKGROUND: Progression-free survival was significantly longer in patients who received avelumab plu...
BACKGROUND: Progression-free survival was significantly longer in patients who received avelumab plu...
Introduction. Simultaneous inhibition of programmed cell death-1 (PD-1)/PD-L1 immune checkpoint and ...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
International audienceBackground: Among patients with advanced renal cell carcinoma (RCC), those wit...
BACKGROUND: Among patients with advanced renal cell carcinoma (RCC), those with sarcomatoid histolog...
BACKGROUND: Antibodies targeting programmed death-1 (PD-1) or programmed death-ligand 1 (PD-L1) have...
The randomized, open-label, phase 3 KEYNOTE-426 study (NCT02853331) demonstrated that pembrolizumab ...
BACKGROUND: In a single-group, phase 1b trial, avelumab plus axitinib resulted in objective respo...
BACKGROUND: In the phase 3 METEOR trial, cabozantinib improved progression-free survival (PFS), obje...
Abstract Although combination immune checkpoint inhibitor (immuno‐oncology [IO]) therapy is the firs...
PURPOSE: To evaluate the association between neutrophil-to-lymphocyte ratio (NLR) and efficacy of av...
Purpose To report updated analyses of the phase III CheckMate 214 trial with extended minimum follow...