alexa Targeting mutated K-ras in pancreatic adenocarcinoma using an adjuvant vaccine.
Toxicology

Toxicology

Journal of Drug Metabolism & Toxicology

Author(s): AbouAlfa GK, Chapman PB, Feilchenfeldt J, Brennan MF, Capanu M, , AbouAlfa GK, Chapman PB, Feilchenfeldt J, Brennan MF, Capanu M,

Abstract Share this page

Abstract PURPOSE: Codon 12 mutations of K-ras are frequent in pancreatic adenocarcinoma, and represent potential tumor-specific neoantigens. The objective of this study was to assess the safety and efficacy of immunizing patients with resected pancreatic cancer with a vaccine targeted against their tumor-specific K-ras mutation. METHODS: Patients with resected pancreatic cancer, with K-ras mutations at codon 12, were vaccinated once monthly for 3 months with a 21-mer peptide vaccine containing the corresponding K-ras mutation of the patient's tumor. About 200 μg of peptide vaccine was injected intradermally on day 7 of a 10-day course of intradermal granulocyte macrophage colony-stimulating factor. Toxicity was assessed by National Cancer Institute Common Toxicity Criteria v2.0. Immune responses were evaluated by delayed-type hypersensitivity (DTH) tests and the enzyme-linked immunosorbent spot assays. RESULTS: Of 62 screened patients, 24 were vaccinated. There were no grade 3-5 vaccine-specific toxicities. The only National Cancer Institute grade 1 and 2 toxicity was erythema at the injection site (94\%). Nine patients (25\%) were evaluable for immunologic responses. One patient (11\%) had a detectable immune response specific to the patient's K-ras mutation, as assessed by DTH. Three patients (13\%) displayed a DTH response that was not specific. Median recurrence free survival time was 8.6 months (95\% confidence interval, 2.96-19.2) and median overall survival time was 20.3 months (95\% confidence interval, 11.6-45.3). CONCLUSIONS: K-ras vaccination for patients with resectable pancreatic adenocarcinoma proved to be safe and tolerable with however no elicitable immunogenicity and unproven efficacy. Future development of adjuvant vaccine therapies should use more immunogenic vaccines. This article was published in Am J Clin Oncol and referenced in Journal of Drug Metabolism & Toxicology

Relevant Expert PPTs

Relevant Speaker PPTs

Recommended Conferences

Relevant Topics

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords