期刊
CLINICAL CANCER RESEARCH
卷 13, 期 15, 页码 4652S-U3出版社
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-07-0213
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MUC1 is a mucinous glycoprotein which is overexpressed and under or aberrantly glycosylated in many human malignancies. MUC1 is associated with cellular transformation and can confer resistance to genotoxic agents. L-BLP25 is a peptide vaccine strategy that targets the exposed core pepticle of MUC1. In preclinical studies, L-BLP25 induced a cellular immune response characterized by T-cell proliferation in response to MUC1 and production of IFN-gamma. Phase I and 11 trials have established the dose and schedule of the vaccine as well as its excellent safety profile. A randomized phase 11 trial of maintenance L-BLP25 versus best supportive care in patients with stage IIIB/ IV non -small cell lung cancer who experienced clinical benefit from initial therapy has been reported. Updated survival analysis of this trial continues to show a strong survival trend in favor of L-BLP25 (median survival, 30.6 versus 13.3 months) in a subgroup of patients with locoregional stage 11113 disease. These promising results will be tested in a phase III trial of L-BLP25 versus placebo in patients with stage III non -small cell lung cancer after response to primary chemoradiotherapy.
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