[HTML][HTML] Dose-dependent effects of NY-ESO-1 protein vaccine complexed with cholesteryl pullulan (CHP-NY-ESO-1) on immune responses and survival benefits of …

S Kageyama, H Wada, K Muro, Y Niwa, S Ueda… - Journal of translational …, 2013 - Springer
S Kageyama, H Wada, K Muro, Y Niwa, S Ueda, H Miyata, S Takiguchi, SH Sugino…
Journal of translational medicine, 2013Springer
Background Cholesteryl pullulan (CHP) is a novel antigen delivery system for cancer
vaccines. This study evaluated the safety, immune responses and clinical outcomes of
patients who received the CHP-NY-ESO-1 complex vaccine, Drug code: IMF-001. Methods
Patients with advanced/metastatic esophageal cancer were enrolled and subcutaneously
vaccinated with either 100 μg or 200 μg of NY-ESO-1 protein complexed with CHP. The
primary endpoints were safety and humoral immune responses, and the secondary endpoint …
Background
Cholesteryl pullulan (CHP) is a novel antigen delivery system for cancer vaccines. This study evaluated the safety, immune responses and clinical outcomes of patients who received the CHP-NY-ESO-1 complex vaccine, Drug code: IMF-001.
Methods
Patients with advanced/metastatic esophageal cancer were enrolled and subcutaneously vaccinated with either 100 μg or 200 μg of NY-ESO-1 protein complexed with CHP. The primary endpoints were safety and humoral immune responses, and the secondary endpoint was clinical efficacy.
Results
A total of 25 patients were enrolled. Thirteen and twelve patients were repeatedly vaccinated with 100 μg or 200 μg of CHP-NY-ESO-1 with a median of 8 or 9.5 doses, respectively. No serious adverse events related to the vaccine were observed. Three out of 13 patients in the 100-μg cohort and 7 out of 12 patients in the 200-μg cohort were positive for anti-NY-ESO-1 antibodies at baseline. In the 100-μg cohort, an antibody response was observed in 5 out of 10 pre-antibody-negatives patients, and the antibody levels were augmented in 2 pre-antibody-positive patients after vaccination. In the 200-μg cohort, all 5 pre-antibody-negative patients became seropositive, and the antibody level was amplified in all 7 pre-antibody-positive patients. No tumor shrinkage was observed. The patients who received 200 μg of CHP-NY-ESO-1 survived longer than patients receiving 100 μg of CHP-NY-ESO-1, even those who exhibited unresponsiveness to previous therapies or had higher tumor burdens.
Conclusions
The safety and immunogenicity of CHP-NY-ESO-1 vaccine were confirmed. The 200 μg dose more efficiently induced immune responses and suggested better survival benefits. (Clinical trial registration number NCT01003808).
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