彭布罗利珠单抗
医学
临床终点
黑色素瘤
肿瘤科
内科学
临床试验
临床研究阶段
癌症研究
转移性黑色素瘤
无进展生存期
癌症
总体生存率
免疫疗法
作者
Lars Ny,Henrik Jespersen,Joakim Karlsson,Samuel Alsén,Stefan Filges,Charlotta All‐Eriksson,Bengt Åndersson,Ana Carneiro,Hildur Helgadóttir,Max Levin,Ingrid Ljuslinder,Roger Olofsson Bagge,Vasu R. Sah,Ulrika Stierner,Anders Ståhlberg,Gustav Ullenhag,Lisa M. Nilsson,Jonas A. Nilsson
标识
DOI:10.1038/s41467-021-25332-w
摘要
Abstract Preclinical studies have suggested that epigenetic therapy could enhance immunogenicity of cancer cells. We report the results of the PEMDAC phase 2 clinical trial ( n = 29; NCT02697630) where the HDAC inhibitor entinostat was combined with the PD-1 inhibitor pembrolizumab in patients with metastatic uveal melanoma (UM). The primary endpoint was objective response rate (ORR), and was met with an ORR of 14%. The clinical benefit rate at 18 weeks was 28%, median progression free survival was 2.1 months and the median overall survival was 13.4 months. Toxicities were manageable, and there were no treatment-related deaths. Objective responses and/or prolonged survival were seen in patients with BAP1 wildtype tumors, and in one patient with an iris melanoma that exhibited a UV signature. Longer survival also correlated with low baseline ctDNA levels or LDH. In conclusion, HDAC inhibition and anti-PD1 immunotherapy results in durable responses in a subset of patients with metastatic UM. Trial registration ClinicalTrials.gov registration number: NCT02697630 (registered 3 March 2016). EudraCT registration number: 2016–002114-50.
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