TY - JOUR
T1 - Unexpected high response rate to traditional therapy after dendritic cell-based vaccine in advanced melanoma
T2 - Update of clinical outcome and subgroup analysis
AU - Ridolfi, Laura
AU - Petrini, Massimiliano
AU - Fiammenghi, Laura
AU - Granato, Anna Maria
AU - Ancarani, Valentina
AU - Pancisi, Elena
AU - Scarpi, Emanuela
AU - Guidoboni, Massimo
AU - Migliori, Giuseppe
AU - Sanna, Stefano
AU - Tauceri, Francesca
AU - Verdecchia, Giorgio Maria
AU - Riccobon, Angela
AU - Ridolfi, Ruggero
PY - 2010
Y1 - 2010
N2 - We reviewed the clinical results of a dendritic cell-based phase II clinical vaccine trial in stage IV melanoma and analyzed a patient subgroup treated with standard therapies after stopping vaccination. From 2003 to 2009, 24 metastatic melanoma patients were treated with mature dendritic cells pulsed with autologous tumor lysate and keyhole limpet hemocyanin and low-dose interleukin-2. Overall response (OR) to vaccination was 37.5% with a clinical benefit of 54.1%. All 14 responders showed delayed type hypersensitivity positivity. Median overall survival (OS) was 15 months (95% CI, 8-33). Eleven patients underwent other treatments (3 surgery, 2 biotherapy, 2 radiotherapy, 2 chemotherapy, and 4 biochemotherapy) after stopping vaccination. Of these, 2 patients had a complete response and 5 a partial response, with an OR of 63.6%. Median OS was 34 months (range 16-61). Our results suggest that therapeutic DC vaccination could favor clinical response in patients after more than one line of therapy.
AB - We reviewed the clinical results of a dendritic cell-based phase II clinical vaccine trial in stage IV melanoma and analyzed a patient subgroup treated with standard therapies after stopping vaccination. From 2003 to 2009, 24 metastatic melanoma patients were treated with mature dendritic cells pulsed with autologous tumor lysate and keyhole limpet hemocyanin and low-dose interleukin-2. Overall response (OR) to vaccination was 37.5% with a clinical benefit of 54.1%. All 14 responders showed delayed type hypersensitivity positivity. Median overall survival (OS) was 15 months (95% CI, 8-33). Eleven patients underwent other treatments (3 surgery, 2 biotherapy, 2 radiotherapy, 2 chemotherapy, and 4 biochemotherapy) after stopping vaccination. Of these, 2 patients had a complete response and 5 a partial response, with an OR of 63.6%. Median OS was 34 months (range 16-61). Our results suggest that therapeutic DC vaccination could favor clinical response in patients after more than one line of therapy.
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U2 - 10.1155/2010/504979
DO - 10.1155/2010/504979
M3 - Article
C2 - 20936106
AN - SCOPUS:78349261932
SN - 1740-2522
VL - 2010
JO - Clinical and Developmental Immunology
JF - Clinical and Developmental Immunology
M1 - 504979
ER -