Emepepimut-S for non-small cell lung cancer

被引:4
作者
Corrales-Rodriguez, Luis
Blais, Normand [2 ]
Soulieres, Denis [1 ]
机构
[1] Univ Montreal, Ctr Hosp, Mol Biol Lab, Montreal, PQ H2L 4M1, Canada
[2] Univ Montreal, Ctr Hosp, Thorac Oncol Grp, Montreal, PQ H2L 4M1, Canada
关键词
BLP-25; emepepimut-S; immunotherapy; liposomal; lung cancer; MUC1; NSCLC; vaccine; BLP25 LIPOSOME VACCINE; BREAST-CANCER; MUCIN GENE; EXPRESSION; ADENOCARCINOMA; IMMUNOTHERAPY; INFLAMMATION; CARCINOMA; PEPTIDES; TRENDS;
D O I
10.1517/14712598.2011.592490
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Immunotherapy as a possible therapeutic option for cancer has been of great importance due to the innovative development of vaccines. Various molecules have been tested and emepepimut-S (Biomira Liposomal Peptide 25 (BLP 25)) has emerged as an option, particularly in lung cancer. Areas covered: A PubMed literature and ClinicalTrials.gov search was conducted using the terms: emepepimut, BLP25, NSCLC, cancer immunotherapy, cancer vaccine and MUC1. This review covers how emepepimut-S acts against the mucin 1 (MUC1) tumor-associated antigen producing a cellular immune response against the cells that express MUC1 and the most important clinical data available that led to the ongoing Phase III trial. Expert opinion: The results obtained in the Phase I/II trials are promising, showing a favorable toxicity with a benefit in survival in NSCLC patients. As future trials develop, demonstration of the long-term survival benefit, understanding of the various mechanisms of immune response initiated by the drug and the selection of patients that will highly benefit from the immunotherapy will be elucidated. The safety and extension in survival makes emepepimut-S a very interesting drug and could, therefore, offer a possibility of treatment and maintenance, particularly for good performance status patients with locally advanced NSCLC.
引用
收藏
页码:1091 / 1097
页数:7
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