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A Perspective on Cell Therapy and Cancer Vaccine in Biliary Tract Cancers (BTCs).

Authors :
Han, Shuting
Lee, Suat Ying
Wang, Who-Whong
Tan, Yu Bin
Sim, Rachel Hui Zhen
Cheong, Rachael
Tan, Cherlyn
Hopkins, Richard
Connolly, John
Shuen, Wai Ho
Toh, Han Chong
Source :
Cancers; Nov2020, Vol. 12 Issue 11, p3404, 1p
Publication Year :
2020

Abstract

Simple Summary: In this review, we discuss treatment strategies in biliary tract cancers (gallbladder cancer, intrahepatic cholangiocarcinoma and extrahepatic cholangiocarcinoma). In particular, we will describe advances in cellular therapies and cancer vaccines for biliary tract cancers, followed by our local experience with combining a melanoma-associated antigen (MAGE)-positive cell lysate-based autologous dendritic cell vaccine and anti-angiogenic therapy (bevacizumab) in a case of stage IV gallbladder cancer. Biliary tract cancer (BTC) is a rare, but aggressive, disease that comprises of gallbladder carcinoma, intrahepatic cholangiocarcinoma and extrahepatic cholangiocarcinoma, with heterogeneous molecular profiles. Advanced disease has limited therapeutic options beyond first-line platinum-based chemotherapy. Immunotherapy has emerged as a viable option for many cancers with a similar unmet need. Therefore, we reviewed current understanding of the tumor immune microenvironment and recent advances in cellular immunotherapy and therapeutic cancer vaccines against BTC. We illustrated the efficacy of dendritic cell vaccination in one patient with advanced, chemorefractory, melanoma-associated antigen (MAGE)-positive gallbladder carcinoma, who was given multiple injections of an allogenic MAGE antigen-positive melanoma cell lysate (MCL)-based autologous dendritic cell vaccine combined with sequential anti-angiogenic therapy. This resulted in good radiological and tumor marker response and an overall survival of 3 years from diagnosis. We postulate the potential synergism of adding anti-angiogenic therapy, such as bevacizumab, to immunotherapy in BTC, as a rational scientific principle to positively modulate the tumor microenvironment to augment antitumor immunity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20726694
Volume :
12
Issue :
11
Database :
Complementary Index
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
147285415
Full Text :
https://doi.org/10.3390/cancers12113404