New developments in autologous tumor cell vaccination therapy for renal cell carcinoma

2000 ◽  
Vol 2 (5) ◽  
pp. 369-371
Author(s):  
Alfons JM van den Eertwegh ◽  
Herbert M. Pinedo
2004 ◽  
Vol 19 (5) ◽  
pp. 570-580 ◽  
Author(s):  
Robert Dillman ◽  
Neil Barth ◽  
Louis VanderMolen ◽  
Khosrow Mahdavi ◽  
Linda Beutel ◽  
...  

2004 ◽  
Vol 19 (5) ◽  
pp. 570-580 ◽  
Author(s):  
Robert Dillman ◽  
Neil Barth ◽  
Louis VanderMolen ◽  
Khosrow Mahdavi ◽  
Linda Beutel ◽  
...  

2001 ◽  
Vol 16 (1) ◽  
pp. 47-54 ◽  
Author(s):  
Robert O. Dillman ◽  
Neil M. Barth ◽  
Louis A. VanderMolen ◽  
David H. Garfield ◽  
Cristina De Leon ◽  
...  

2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 14585-14585
Author(s):  
T. F. Wimpissinger ◽  
T. Felzmann ◽  
H. Hügel ◽  
P. Funovics ◽  
W. Stackl

14585 Background: We have conducted a clinical phase I trial to evaluate feasibility and safety of dendritic cell-based immunotherapy in patients with advanced renal cell carcinoma (RCC). As opposed to previous cancer vaccination studies, dendritic cells were specifically enabled to secrete interleukin 12 (IL-12). Methods: Patients with advanced RCC (n = 11) received six weekly intranodal vaccinations with autologous monocyte-derived dendritic cells (mDCs). MDCs were loaded with autologous tumor cell lysate and were specifically stimulated to secrete IL-12 to polarize type-1 T-helper lymphocytes (Th1) and to directly present tumor antigens to cytotoxic T lymphocytes (CTL). Results: There was no significant treatment-related toxicity and no clinical evidence of autoimmunity. Vaccination was very well tolerated. Five patients had stable disease for at least five months, while four patients had progressive disease. Two patients with early clinically significant disease progression had to be excluded before completion of the treatment. In addition, we could detect enhanced anti-tumor immunity in vitro comparing immune response before versus after cancer vaccination. Conclusions: Our findings indicate that cancer vaccination with IL-12 secreting mDCs is well tolerated and has potential clinical and clear immunological effects in patients with advanced RCC. No significant financial relationships to disclose.


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