| Literature DB >> 29358173 |
Sumiyuki Nishida1, Takeshi Ishikawa2, Shinichi Egawa3, Shigeo Koido4, Hiroaki Yanagimoto5, Jun Ishii6, Yoshihide Kanno7, Satoshi Kokura2, Hiroaki Yasuda2, Mari Saito Oba8, Maho Sato8, Soyoko Morimoto9, Fumihiro Fujiki10, Hidetoshi Eguchi11, Hiroaki Nagano11, Atsushi Kumanogoh12,13, Michiaki Unno14, Masanori Kon5, Hideaki Shimada6, Kei Ito7, Sadamu Homma15, Yoshihiro Oka13,16, Satoshi Morita17, Haruo Sugiyama10.
Abstract
We investigated the efficacy of a Wilms' tumor gene 1 (WT1) vaccine combined with gemcitabine (GEMWT1) and compared it with gemcitabine (GEM) monotherapy for advanced pancreatic ductal adenocarcinoma (PDAC) in a randomized phase II study. We randomly assigned HLA-A*02:01- or HLA-A*24:02-positive patients with advanced PDAC to receive GEMWT1 or GEM. We assessed WT1-specific immune responses via delayed-type hypersensitivity (DTH) to the WT1 peptide and a tetramer assay to detect WT1-specific cytotoxic T lymphocytes (WT1-CTL). Of 91 patients enrolled, 85 were evaluable (GEMWT1: n = 42; GEM: n = 43). GEMWT1 prolonged progression-free survival [PFS; hazard ratio (HR), 0.66; P = 0.084] and improved overall survival rate at 1 year (1-year OS%; GEMWT1: 35.7%; GEM: 20.9%). However, the difference in OS was not significant (HR: 0.82; P = 0.363). These effects were particularly evident in metastatic PDAC (PFS: HR 0.51, P = 0.0017; 1-year OS%: GEMWT1 27.3%; GEM 11.8%). The combination was well tolerated, with no unexpected serious adverse events. In patients with metastatic PDAC, PFS in the DTH-positive GEMWT1 group was significantly prolonged, with a better HR of 0.27 compared with the GEM group, whereas PFS in the DTH-negative GEMWT1 group was similar to that in the GEM group (HR 0.86; P = 0.001). DTH positivity was associated with an increase in WT1-CTLs induced by the WT1 vaccine. GEM plus the WT1 vaccine prolonged PFS and may improve 1-year OS% in advanced PDAC. These clinical effects were associated with the induction of WT1-specific immune responses. Cancer Immunol Res; 6(3); 320-31. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29358173 DOI: 10.1158/2326-6066.CIR-17-0386
Source DB: PubMed Journal: Cancer Immunol Res ISSN: 2326-6066 Impact factor: 11.151