Table 3.

Vaccine generated by loading tumor antigen onto antigen-presenting cells ex vivo

DiseasePeptide/protein or whole cell as antigen sourceNImmune responseClinical responseReference
Myeloma Idiotype-loaded antigen-presenting cells (Mylovenge) following autologous transplantation 27 patients vaccinated; compared with historical control group of 124 patients Not assessed Median PFS 1.5 y both arms.Median OS vaccine group: 5.3 y vs 3.4 y in controls.P = .02 59  
Follicular lymphoma Idiotype-pulsed DC 10 patients with active disease T-cell response in 8/10 patients 4/10 patients demonstrate response, including 2 CR 60  
25 patients in remission after chemotherapy 23 evaluable patients, T-cell or humoral anti-Id response in 65% 70% remained without disease progression at 43 mo after completion of chemotherapy 
AML DC electroporated with WT1 mRNA 30 AML patients, in remission after chemotherapy At least a 1.5-fold increase in WT1 tetramer-positive CD8+ T cells in 6 of 12 evaluable patients Clinical response rate 43% 61  
AML DCs pulsed with hTERT 24 AML patients, in remission T-cell responses targeting t-HERT were observed in 58% of patients 58% of patients remained in remission with a median follow-up of 52 mo 62  
Myeloma Whole cell DC/myeloma fusion 17 patients Vaccination resulted in the expansion of circulating CD4 and CD8 lymphocytes reactive with autologous myeloma cells in 11/15 evaluable patients Disease stabilization in 66% of patients 66  
AML Whole cell DC/AML fusion 17 patients, vaccinated in CR1 Durable expansion of leukemia-reactive T cells in the blood and bone marrow 71% of patients alive with median follow up of 57 mo 67  
Myeloma Whole cell DC/myeloma fusion 36 patients vaccinated All evaluable patients had at least a twofold expansion of myeloma-specific CD4+ and/or CD8+ T cells 31% achieved a CR/nCR in the early posttransplant period, whereas an additional 17% achieved CR/nCR only after day 100 posttransplant after undergoing vaccination 69  
DiseasePeptide/protein or whole cell as antigen sourceNImmune responseClinical responseReference
Myeloma Idiotype-loaded antigen-presenting cells (Mylovenge) following autologous transplantation 27 patients vaccinated; compared with historical control group of 124 patients Not assessed Median PFS 1.5 y both arms.Median OS vaccine group: 5.3 y vs 3.4 y in controls.P = .02 59  
Follicular lymphoma Idiotype-pulsed DC 10 patients with active disease T-cell response in 8/10 patients 4/10 patients demonstrate response, including 2 CR 60  
25 patients in remission after chemotherapy 23 evaluable patients, T-cell or humoral anti-Id response in 65% 70% remained without disease progression at 43 mo after completion of chemotherapy 
AML DC electroporated with WT1 mRNA 30 AML patients, in remission after chemotherapy At least a 1.5-fold increase in WT1 tetramer-positive CD8+ T cells in 6 of 12 evaluable patients Clinical response rate 43% 61  
AML DCs pulsed with hTERT 24 AML patients, in remission T-cell responses targeting t-HERT were observed in 58% of patients 58% of patients remained in remission with a median follow-up of 52 mo 62  
Myeloma Whole cell DC/myeloma fusion 17 patients Vaccination resulted in the expansion of circulating CD4 and CD8 lymphocytes reactive with autologous myeloma cells in 11/15 evaluable patients Disease stabilization in 66% of patients 66  
AML Whole cell DC/AML fusion 17 patients, vaccinated in CR1 Durable expansion of leukemia-reactive T cells in the blood and bone marrow 71% of patients alive with median follow up of 57 mo 67  
Myeloma Whole cell DC/myeloma fusion 36 patients vaccinated All evaluable patients had at least a twofold expansion of myeloma-specific CD4+ and/or CD8+ T cells 31% achieved a CR/nCR in the early posttransplant period, whereas an additional 17% achieved CR/nCR only after day 100 posttransplant after undergoing vaccination 69  

hTERT, human telomerase reverse transcriptase; Id, idiotype; nCR, near complete response; t-HERT, telomerase reverse transcriptase. Other abbreviations are explained in Table 1.

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