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Liver cancer is one of the most common malignancies worldwide and the leading cause of cancer-related death
Results of cohort 1 of the KEYNOTE-224 trial showed that pembrolizumab was effective and well tolerated in patients with advanced HCC previously treated with sorafenib
Pembrolizumab was effective and well tolerated in patients with advanced HCC previously treated with sorafenib
The KEYNOTE-224 trial is an open-label, multi-country, phase II clinical trial that enrolled 2 cohorts of patients with advanced HCC who had not received prior systemic therapy and were unsuitable or refractory to local therapy, and were treated with pembrolizumab (200 mg/kg/day).
Secondary endpoints included duration of response, disease control rate, time to progression, progression-free survival, overall survival, and safety/tolerability
51 The objective response rate was 16% The objective response rate was 16% The median duration of response was 16 months, and the disease control rate was 57% The median duration of response was 16 months, and the disease control rate was 57%
In conclusion, in patients with advanced HCC who have not received prior systemic therapy, pembrolizumab therapy provided durable antitumor activity, promising overall survival, and a safety profile consistent with previous reports
In patients with advanced HCC who have not received prior systemic therapy, pembrolizumab treatment provides durable antitumor activity, promising overall survival, and a safety profile consistent with previous reports in patients with advanced HCC who have not received prior systemic therapy pembrolizumab therapy provided durable antitumor activity, promising overall survival, and a safety profile consistent with previous reports
Original source:
Original source:Gontran Verset, Ivan Borbath, Mark Karwal, et al.
Gontran Verset, Ivan Borbath, Mark Karwal, et al.
Pembrolizumab Monotherapy for Previously Untreated Advanced Hepatocellular Carcinoma: Data from the Open-Label, Phase II KEYNOTE-224 Trial.
Clin Cancer Res 2022; https://doi.
org/10.
1158/ 1078-0432.
CCR-21-3807
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