Schellens5 1University of Pennsylvania, Philadelphia/PA/United States of America, 2Drug Development Unit, Institute of Cancer Research, Sutton/ United Kingdom, 3Istituto Clinico Humanitas, Milan/Italy, 4Merck & Co., Inc., Kenilworth/NJ/United States of America, 5Netherlands Cancer Institute, Plesmanlaan/ Netherlands; 12 patients had stable disease, resulting in a disease control rate of 76%; median duration of response was 9.2 months; median progression-free survival was 5.8 months, with 6- and 12-month PFS rates of 50% and 25%, respectively
Median overall survival was 18.0 months with 6- and 12-month OS rates of 83.5% and 62.6%, respectively
Long-term administration of pembrolizumab is feasible in patients with MPM, and no new safety signals were identified
KEYNOTE-028 is a nonrandomized, multicohort phase 1b trial of pembrolizumab in patients with PD-L1epositive advanced solid tumors. 25 patients with MPM were treated with pembrolizumab in the mesothelioma cohort
We examined biopsy specimens from 12 Malignant pleural mesothelioma patients that were removed during maximal cyto-reductive surgery
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