Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Jan;5(1):81-9.
doi: 10.1177/1758834012462463.

Immunotherapy updates in pancreatic cancer: are we there yet?

Affiliations

Immunotherapy updates in pancreatic cancer: are we there yet?

Krishna Soujanya Gunturu et al. Ther Adv Med Oncol. 2013 Jan.

Abstract

Pancreatic cancer is a lethal disease and remains one of the most resistant cancers to traditional therapies. Historically, chemotherapy or radiotherapy did not provide meaningful survival benefit in advanced pancreatic cancer. Gemcitabine and recently FOLFIRINOX (5-flourouracil, leucovorin, oxaliplatin and irinotecan) have provided some limited survival advantage in advanced pancreatic cancer. Targeted agents in combination with gemcitabine had not shown significant improvement in the survival. Current therapies for pancreatic cancer have their limitations; thus, we are in dire need of newer treatment options. Immunotherapy in pancreatic cancer works by recruiting and activating T cells that recognize tumor-specific antigens which is a different mechanism compared with chemotherapy and radiotherapy. Preclinical models have shown that immunotherapy and targeted therapies like vascular endothelial growth factor and epidermal growth factor inhibitors work synergistically. Hence, new immunotherapy and targeted therapies represent a viable option for pancreatic cancer. In this article, we review the vaccine therapy for pancreatic cancer.

Keywords: immunotherapy; pancreatic cancer; vaccine.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest statement: Gabriela R. Rossi has received honoraria from NewLink Genetics Corporation.

Similar articles

Cited by

References

    1. Abou-Alfa G., Chapman P., Feilchenfeldt J., Brennan M., Capanu M., Gansukh B., et al. (2011) Targeting mutated K-ras in pancreatic adenocarcinoma using an adjuvant vaccine. Am J Clin Oncol 34: 321–325 - PubMed
    1. Abrams S., Khleif S., Bergmann-Leitner E., Kantor J., Chung Y., Hamilton J., et al. (1997) Generation of stable CD4+ and CD8+ T cell lines from patients immunized with ras oncogene-derived peptides reflecting codon 12 mutations. Cell Immunol 182: 137–151 - PubMed
    1. Almoguera C., Shibata D., Forrester K., Martin J., Arnheim N., Perucho M. (1988) Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes. Cell 53: 549–554 - PubMed
    1. Bernhardt S., Gjertsen M., Trachsel S., Moller M., Eriksen J., Meo M., et al. (2006) Telomerase peptide vaccination of patients with non-resectable pancreatic cancer: A dose escalating phase I/II study. Br J Cancer 95: 1474–1482 - PMC - PubMed
    1. Bilimoria K., Bentrem D., Clifford Y., Ritchey J., Wincester D., Talamonti M. (2007) Validation of the 6th Edition AJCC Pancreatic Cancer Staging System: report from the National Cancer Database. Cancer 110: 738–744 - PubMed

LinkOut - more resources