TY - JOUR
T1 - Peptide vaccine as an adjuvant therapy for glypican-3-positive hepatocellular carcinoma induces peptide-specific CTLs and improves long prognosis
AU - Taniguchi, Masatake
AU - Mizuno, Shoichi
AU - Yoshikawa, Toshiaki
AU - Fujinami, Norihiro
AU - Sugimoto, Motokazu
AU - Kobayashi, Shin
AU - Takahashi, Shinichiro
AU - Konishi, Masaru
AU - Gotohda, Naoto
AU - Nakatsura, Tetsuya
N1 - Funding Information:
The authors would like to thank Kayoko Shoda and Yukiko Kozaki for their technical assistance. We would like to thank Editage ( www.editage.jp ) for English language editing. This work was supported by the National Cancer Center Research and Development Fund under Grant [25‐A‐7 and 28‐A‐8]; and by joint research funding from Thyas Co., Ltd. and Sysmex Co., Ltd.
Funding Information:
Tetsuya Nakatsura is a founder of and current shareholder at Killer T Save You Co., Ltd. TN is currently receiving royalties from Onco Therapy Science, Inc and fundamental research funding support from Thyas Co., Ltd. and Sysmex Co., Ltd. The remaining authors declare that they have no commercial or financial relationships that could be construed as a potential conflict of interest.
Funding Information:
The authors would like to thank Kayoko Shoda and Yukiko Kozaki for their technical assistance. We would like to thank Editage (www.editage.jp) for English language editing. This work was supported by the National Cancer Center Research and Development Fund under Grant [25-A-7 and 28-A-8]; and by joint research funding from Thyas Co., Ltd. and Sysmex Co., Ltd.
Publisher Copyright:
© 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association
PY - 2020/8/1
Y1 - 2020/8/1
N2 - There is no established postoperative adjuvant therapy for hepatocellular carcinoma (HCC), and improvement of patient prognosis has been limited. We conducted long-term monitoring of patients within a phase II trial that targeted a cancer antigen, glypican-3 (GPC3), specifically expressed in HCC. We sought to determine if the GPC3 peptide vaccine was an effective adjuvant therapy by monitoring disease-free survival and overall survival. We also tracked GPC3 immunohistochemical (IHC) staining, CTL induction, and postoperative plasma GPC3 for a patient group that was administered the vaccine (n = 35) and an unvaccinated patient group that underwent surgery only (n = 33). The 1-y recurrence rate after surgery was reduced by approximately 15%, and the 5-y and 8-y survival rates were improved by approximately 10% and 30%, respectively, in the vaccinated group compared with the unvaccinated group. Patients who were positive for GPC3 IHC staining were more likely to have induced CTLs, and 60% survived beyond 5 y. Vaccine efficacy had a positive relationship with plasma concentration of GPC3; high concentrations increased the 5-y survival rate to 75%. We thus expect GPC3 vaccination in patients with HCC, who are positive for GPC3 IHC staining and/or plasma GPC3 to induce CTL and have significantly improved long-term prognosis.
AB - There is no established postoperative adjuvant therapy for hepatocellular carcinoma (HCC), and improvement of patient prognosis has been limited. We conducted long-term monitoring of patients within a phase II trial that targeted a cancer antigen, glypican-3 (GPC3), specifically expressed in HCC. We sought to determine if the GPC3 peptide vaccine was an effective adjuvant therapy by monitoring disease-free survival and overall survival. We also tracked GPC3 immunohistochemical (IHC) staining, CTL induction, and postoperative plasma GPC3 for a patient group that was administered the vaccine (n = 35) and an unvaccinated patient group that underwent surgery only (n = 33). The 1-y recurrence rate after surgery was reduced by approximately 15%, and the 5-y and 8-y survival rates were improved by approximately 10% and 30%, respectively, in the vaccinated group compared with the unvaccinated group. Patients who were positive for GPC3 IHC staining were more likely to have induced CTLs, and 60% survived beyond 5 y. Vaccine efficacy had a positive relationship with plasma concentration of GPC3; high concentrations increased the 5-y survival rate to 75%. We thus expect GPC3 vaccination in patients with HCC, who are positive for GPC3 IHC staining and/or plasma GPC3 to induce CTL and have significantly improved long-term prognosis.
KW - cytotoxic T lymphocyte
KW - glypican-3
KW - hepatocellular carcinoma
KW - immunohistochemical staining
KW - peptide vaccine
UR - http://www.scopus.com/inward/record.url?scp=85087211333&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85087211333&partnerID=8YFLogxK
U2 - 10.1111/cas.14497
DO - 10.1111/cas.14497
M3 - Article
C2 - 32449239
AN - SCOPUS:85087211333
SN - 1347-9032
VL - 111
SP - 2747
EP - 2759
JO - Cancer Science
JF - Cancer Science
IS - 8
ER -