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Document type:
journal article 
Author(s):
Brill, TH; Kübler, HR; Pohla, H; Buchner, A; Fend, F; Schuster, T; von Randenborgh, H; Paul, R; Kummer, T; Plank, C; Eisele, B; Breul, J; Hartung, R; Schendel, DJ; Gansbacher, B 
Title:
Therapeutic vaccination with an interleukin-2-interferon-gamma-secreting allogeneic tumor vaccine in patients with progressive castration-resistant prostate cancer: a phase I/II trial. 
Abstract:
Immunotherapy with whole cell cancer vaccines has been tested in various tumor types. This study investigated the safety profile and antitumor activity of an allogeneic prostate carcinoma cell line, LNCaP, expressing recombinant human interleukin-2 and human interferon-gamma. Thirty HLA-A*0201-matched patients with progressive, castration-resistant prostate cancer received four intradermal injections on days 1, 15, 29, and 92, and then every 90 days, as long as no tumor progression occurred. Three patients received a dose level of 7.5 million cells, and 27 patients received 15 million cells per injection. The primary study criteria were safety and the difference in prostate-specific antigen doubling time (PSA-DT), determined in the pretreatment phase (before the start of vaccination) and in the trial treatment phase (during vaccination). No dose-limiting or autoimmune toxicity was seen. During vaccination there was a significant prolongation of the PSA-DT compared with the prevaccination period (prolongationfrom 63 to 114 days; p< 0.01; intention to treat). In addition, results showed a period of PSA stabilization of at least 12 weeks, together with stable bone scans in 12 of 30 patients, and 3 patients sustained a>50% decrease in PSA versus baseline. The median overall survival time from first vaccination was 32 months (mean value, 34 months). Immune monitoring revealed T cell stimulation in the majority of patients. This vaccine strategy was found to be safe and well tolerated and was accompanied by prolongation of PSA-DT. The results of this trial warrant clinical development of this vaccine. 
Journal title abbreviation:
Hum Gene Ther 
Year:
2009 
Journal volume:
20 
Journal issue:
12 
Pages contribution:
1641-51 
Language:
eng 
Print-ISSN:
1043-0342 
TUM Institution:
Institut für experimentelle Onkologie und Therapieforschung ; Urologische Klinik und Poliklinik ; Institut für Medizinische Statistik und Epidemiologie 
Format:
Text