Table 1.

Peptide- or protein-based vaccines, without exogenous antigen-presenting cell

DiseasePeptide/proteinNImmune responseClinical responseReference
AML/MDS WT1 51 reviews of data from 9 clinical trials 2.4-fold expansion of WT1-specific T cells. Immune response analyzed from 4 trials (n = 23) in which WT1-specific expansion was assessed without ex vivo stimulation. In each of 9 clinical trials, clinical responses were observed, including a patient who remained in CR for >8 y in 1 study. 24  
AML/ MDS WT1 16 Significant expansion of WT1 tetramer-positive CD8 T cells was not observed. 1 of 2 MDS patients demonstrated decrease in transfusion requirement and a transient reduction in blasts. 36  
Median time to recurrence in 14 AML patients was 244 d. 
AML/MDS CML PR1 66 Doubling of PR1 tetramer-positive T cells in 53% of patients 24% clinical response (8 patients CR; 1 patient PR; 3 patients demonstrated hematologic improvement) 37  
Multiple myeloma Idiotype DNA vaccine linked to FrC of tetanus toxoid 15 71% immune response to FrC Median TTP 38 mo 18  
29% immune response to idiotype OS 64% after median follow-up of 85.6 mo 
Multiple myeloma Peptides derived from Bcl-2 family proteins with montanide Immune response noted in all 6 patients who received more than two vaccines No disease regression 43  
Follicular lymphoma Idiotype MyVax, randomized trial 287 patients Anti-idiotype immune response was associated with longer PFS Median PFS 19.1 mo, not a statistically significant difference from control group 40  
Follicular lymphoma Idiotype vaccine Favrille study, randomized trial 349 patients Immune response was not assessed Median TTP was 9 mo in vaccine arm vs 12.6 mo in control (P = .019). The shorter TTP in the vaccine arm was speculated to relate to differences in FLIPI scores. 41  
Follicular lymphoma Idiotype Biovaxid 234 patients Immune response was not reported Median DFS was significantly higher in vaccinated patients (44.2 mo) compared with control (30.6 mo; P = .05) 42  
DiseasePeptide/proteinNImmune responseClinical responseReference
AML/MDS WT1 51 reviews of data from 9 clinical trials 2.4-fold expansion of WT1-specific T cells. Immune response analyzed from 4 trials (n = 23) in which WT1-specific expansion was assessed without ex vivo stimulation. In each of 9 clinical trials, clinical responses were observed, including a patient who remained in CR for >8 y in 1 study. 24  
AML/ MDS WT1 16 Significant expansion of WT1 tetramer-positive CD8 T cells was not observed. 1 of 2 MDS patients demonstrated decrease in transfusion requirement and a transient reduction in blasts. 36  
Median time to recurrence in 14 AML patients was 244 d. 
AML/MDS CML PR1 66 Doubling of PR1 tetramer-positive T cells in 53% of patients 24% clinical response (8 patients CR; 1 patient PR; 3 patients demonstrated hematologic improvement) 37  
Multiple myeloma Idiotype DNA vaccine linked to FrC of tetanus toxoid 15 71% immune response to FrC Median TTP 38 mo 18  
29% immune response to idiotype OS 64% after median follow-up of 85.6 mo 
Multiple myeloma Peptides derived from Bcl-2 family proteins with montanide Immune response noted in all 6 patients who received more than two vaccines No disease regression 43  
Follicular lymphoma Idiotype MyVax, randomized trial 287 patients Anti-idiotype immune response was associated with longer PFS Median PFS 19.1 mo, not a statistically significant difference from control group 40  
Follicular lymphoma Idiotype vaccine Favrille study, randomized trial 349 patients Immune response was not assessed Median TTP was 9 mo in vaccine arm vs 12.6 mo in control (P = .019). The shorter TTP in the vaccine arm was speculated to relate to differences in FLIPI scores. 41  
Follicular lymphoma Idiotype Biovaxid 234 patients Immune response was not reported Median DFS was significantly higher in vaccinated patients (44.2 mo) compared with control (30.6 mo; P = .05) 42  

CR, complete response; DFS, disease-free survival; FLIPI, follicular lymphoma international prognostic index; FrC, fragment C; OS, overall survival; PR, prognostic index; TTP, time to progression.

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