» Articles » PMID: 25314223

Translation of Genomics-guided RNA-based Personalised Cancer Vaccines: Towards the Bedside

Overview
Journal Br J Cancer
Specialty Oncology
Date 2014 Oct 15
PMID 25314223
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer is a disease caused by DNA mutations. Cancer therapies targeting defined functional mutations have shown clinical benefit. However, as 95% of the mutations in a tumour are unique to that single patient and only a small number of mutations are shared between patients, the addressed medical need is modest. A rapidly determined patient-specific tumour mutation pattern combined with a flexible mutation-targeting drug platform could generate a mutation-targeting individualised therapy, which would benefit each single patient. Next-generation sequencing enables the rapid identification of somatic mutations in individual tumours (the mutanome). Immunoinformatics enables predictions of mutation immunogenicity. Mutation-targeting RNA-based vaccines can be rapidly and affordably synthesised as custom GMP drug products. Integration of these cutting-edge technologies into a clinically applicable process holds the promise of a disruptive innovation benefiting cancer patients. Here, we describe our translation of the individualised RNA-based cancer vaccine concept into clinic trials.

Citing Articles

A Phase I/II trial comparing autologous dendritic cell vaccine pulsed either with personalized peptides (PEP-DC) or with tumor lysate (OC-DC) in patients with advanced high-grade ovarian serous carcinoma.

Sarivalasis A, Boudousquie C, Balint K, Stevenson B, Gannon P, Iancu E J Transl Med. 2019; 17(1):391.

PMID: 31771601 PMC: 6880492. DOI: 10.1186/s12967-019-02133-w.


A library of Neo Open Reading Frame peptides (NOPs) as a sustainable resource of common neoantigens in up to 50% of cancer patients.

Koster J, Plasterk R Sci Rep. 2019; 9(1):6577.

PMID: 31036835 PMC: 6488612. DOI: 10.1038/s41598-019-42729-2.


Personalized Dendritic Cell Vaccines-Recent Breakthroughs and Encouraging Clinical Results.

Mastelic-Gavillet B, Balint K, Boudousquie C, Gannon P, Kandalaft L Front Immunol. 2019; 10:766.

PMID: 31031762 PMC: 6470191. DOI: 10.3389/fimmu.2019.00766.


Cancer immunotherapy-targeted glypican-3 or neoantigens.

Shimizu Y, Suzuki T, Yoshikawa T, Tsuchiya N, Sawada Y, Endo I Cancer Sci. 2017; 109(3):531-541.

PMID: 29285841 PMC: 5834776. DOI: 10.1111/cas.13485.


Taking a Stab at Cancer; Oncolytic Virus-Mediated Anti-Cancer Vaccination Strategies.

Aitken A, Roy D, Bourgeois-Daigneault M Biomedicines. 2017; 5(1).

PMID: 28536346 PMC: 5423491. DOI: 10.3390/biomedicines5010003.


References
1.
Li H, Durbin R . Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009; 25(14):1754-60. PMC: 2705234. DOI: 10.1093/bioinformatics/btp324. View

2.
Rahma O, Ashtar E, Ibrahim R, Toubaji A, Gause B, Herrin V . A pilot clinical trial testing mutant von Hippel-Lindau peptide as a novel immune therapy in metastatic renal cell carcinoma. J Transl Med. 2010; 8:8. PMC: 2843651. DOI: 10.1186/1479-5876-8-8. View

3.
Weide B, Garbe C, Rammensee H, Pascolo S . Plasmid DNA- and messenger RNA-based anti-cancer vaccination. Immunol Lett. 2007; 115(1):33-42. DOI: 10.1016/j.imlet.2007.09.012. View

4.
Kenter G, Welters M, Valentijn A, Lowik M, Berends-van der Meer D, Vloon A . Vaccination against HPV-16 oncoproteins for vulvar intraepithelial neoplasia. N Engl J Med. 2009; 361(19):1838-47. DOI: 10.1056/NEJMoa0810097. View

5.
Stratton M . Exploring the genomes of cancer cells: progress and promise. Science. 2011; 331(6024):1553-8. DOI: 10.1126/science.1204040. View