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. 2021 Jul 7;13(14):3400. doi: 10.3390/cancers13143400

Table 1.

Summary of clinical trials for vaccines against GBM.

NCT Number Treatment Summary of Results Indication References
NCT00643097 EGFRvIII peptide vaccine + DI-TMZ EGFRvIII-expressing cells eradicated and vaccine immunogenic, with DI-TMZ cohort having enhanced humoral response. Median overall survival of 23.6 months. Primary GBM Sampson et al. [13]
Sampson et al. [14]
NCT00458601 EGFRvIII peptide vaccine + TMZ Median overall survival of 21.8 months and 36-month survival of 26%. Anti-EGFRvIII antibodies increased ≥4-fold in 85% of patients with duration of treatment. Primary GBM Schuster et al. [15]
NCT01480479 EGFRvIII peptide vaccine + TMZ Strong humoral responses; however, no survival advantage and loss of EGFRvIII expression upon recurrence. Primary GBM Weller et al. [16]
NCT01498328 EGFRvIII peptide vaccine + bevacizumab 24-month survival of 20% compared to 3% for controls. Recurrent GBM Reardon et al. [17]
NCT00639639 CMV pp65 DC vaccine + Td Toxoid + TMZ Td toxoid pre-conditioning enhanced DC migration to the lymph nodes and improved survival. 3/6 Td toxoid patients were alive and progression-free at time of survival analysis (>36.6 months), while controls had median overall survival of 18.5 months. Primary GBM Mitchell et al. [18]
NCT00639639 CMV pp65 DC vaccine + DI-TMZ Antigen-specific immune responses and median overall survival of 41.1 months in DI-TMZ cohort. A total of 36% survival 5 years from diagnosis, with four patients remaining progression-free at 59–64 months from diagnosis. Primary GBM Batich et al. [19]
NCT02366728 CMV pp65 DC vaccine + 111In-labeled DC vaccine + Td Toxoid + basiliximab Ongoing, have reported increased DC migration to lymph nodes following Td toxoid pre-conditioning. Primary GBM Batich et al. [20]
NCT02454634 IDH1 peptide vaccine A total of 93% vaccine-specific response rate, 84% survival >3 years. High-grade glioma Platten et al. [21]
NCT00045968 DCVax-L vaccine Median overall survival of 23.1 months, with large group (n = 100) reaching 40.5 months. Primary GBM Liau et al. [22]
NCT00293423 HSPPC-96 peptide vaccine Specific immune response in 11 of the 12 patients, responders had median overall survival of 11.8 months. Recurrent GBM Crane et al. [23]
Bloch et al. [24]
NCT02122822 HSPPC-96 peptide vaccine + TMZ + radiotherapy Median overall survival of 31.4 months. Patients with high tumor-specific immune responses had median overall survival of >40.5 months compared to 14.6 months for low responders. Primary GBM Ji et al. [25]
NCT00905060 HSPPC-96 vaccine + TMZ Median overall survival of 23.8 months. Patients with low PD-L1 expression in myeloid cells had median overall survival of 44.7 months compared to 18 months for those with high expression. Primary GBM Bloch et al. [26]