Therapeutic dendritic cell vaccination of patients with metastatic renal cell carcinoma - A clinical, phase 1/2 trial

被引:81
作者
Berntsen, Annika [1 ]
Trepiakas, Redas [1 ]
Wenandy, Lynn [4 ]
Geertsen, Poul F. [1 ]
Straten, Per thor [4 ]
Andersen, Mads H. [4 ]
Pedersen, Anders E. [5 ]
Claesson, Mogens H. [5 ]
Lorentzen, Torben [2 ]
Johansen, Julia S. [3 ]
Svane, Inge Marie [1 ,4 ]
机构
[1] Herlev Hosp, CCIT, Dept Oncol, DK-2730 Herlev, Denmark
[2] Herlev Hosp, CCIT, Dept Radiol, DK-2730 Herlev, Denmark
[3] Herlev Hosp, CCIT, Dept Rheumatol, DK-2730 Herlev, Denmark
[4] Herlev Hosp, CCIT, Dept Hematol, DK-2730 Herlev, Denmark
[5] Univ Copenhagen, Panum Inst, Inst Int Hlth Immunol & Microbiol, DK-1168 Copenhagen, Denmark
关键词
renal cell carcinoma; dendritic cell; cancer vaccination; YKL-40; IL-6;
D O I
10.1097/CJI.0b013e3181833818
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapeutic dendritic cell (DC) vaccination against cancer is a strategy aimed at activating the immune system to recognize and destroy tumor cells. In this nonrandomized phase 1/2 trial, we investigated the safety, feasibility, induction of T-cell response, and clinical response after treatment with a DC- based vaccine in patients with metastatic renal cell carcinoma. Twenty-seven patients with progressive cytokine-refractory metastatic renal cell carcinoma were vaccinated with DCs loaded with either a cocktail of survivin and telomerase peptides or tumor lysate depending on their HLA-A2 haplotype, and low-dose IL-2 was administered concomitantly. Tumor response, immune response, and serum IL-6 and YKL-40 were measured during treatment. Vaccine generation was Successful in all patients and no serious adverse events were observed. None of the patients had an objective response but 13/27 patients obtained disease stabilization (SD) for more than 8 weeks. An antigen-specific immune response was demonstrated in 6/6 patients tested. Furthermore, significant alterations in serum YKL-40 and IL-6 were found during treatment. In conclusion, DC vaccination in our setting is feasible and without severe toxicity. Almost half of the patients obtained SID, and in more than 1/3 of the patients, SD persisted for more than 6 months. However, the evaluation of SD is difficult to interpret in the absence of a randomized trial and, therefore, these results should be interpreted with caution. Antigen-specific immune responses were observed in a subset of the treated patients.
引用
收藏
页码:771 / 780
页数:10
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