Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Shankar K. Nayak"'
Autor:
Robert O. Dillman, Linda D. Beutel, Shankar K. Nayak, Carol DePriest, Senthamil R. Selvan, Patric M. Schiltz
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 20:373-378
Determination of potency is a challenging problem for patient-specific products derived from autologous cells. For several years, we have been investigating the safety and therapeutic potential of patient- specific vaccines derived from short-term au
Autor:
Linda D. Beutel, Louis A. VanderMolen, Robert O. Dillman, Cristina de Leon, Carol DePriest, Neil M. Barth, Khosrow Mahdavi, Shankar K. Nayak
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 19:570-580
We previously reported the laboratory methodology for producing patient-specific irradiated autologous tumor-cell products derived from short-term cultured tumor cells from resected renal cell carcinoma, and described preliminary clinical results. In
Phase I/II Trial of Autologous Tumor Cell Line–Derived Vaccines for Recurrent or Metastatic Sarcomas
Autor:
Cheryl Peterson, Linda D. Beutel, Shankar K. Nayak, Senthamil R. Selvan, Robert O. Dillman, Neil M. Barth, Cristina de Leon, Carol DePriest
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 19:581-588
We previously reported the laboratory methodology for producing patient-specific irradiated autologous tumor-cell products derived from short-term cultured tumor cells. We attempted to determine the feasibility, safety, and clinical effects of autolo
Publikováno v:
Journal of Immunotherapy. 26:367-373
The objective was to study the effects of patient-specific vaccine immunotherapy administered with either interferon-gamma (IFNgamma) or granulocyte-macrophage colony stimulating factor (GM-CSF) in patients with metastatic cancer. Short-term cell lin
Autor:
Linda D. Beutel, Robert O. Dillman, Shankar K. Nayak, Audrey A. O'Connor, Neil M. Barth, B. S. N. Carol Depriest, Cristina de Leon
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 17:51-66
We established short-term cultures of pure tumor cells for use as autologous tumor cell vaccines in an effort to study the effects of patients-specific immunotherapy.Surgically resected fresh tumor was obtained from patients with metastatic cancer. S
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 16:205-211
We tried to establish short-term cultures of autologous tumors from patients with breast carcinoma for potential use as active specific immunotherapy (i.e., autologous vaccine) after resection of primary breast cancer, and/or for the treatment of met
Autor:
Louis A. VanderMolen, Audrey A. O'Connor, Robert O. Dillman, Neil M. Barth, David H. Garfield, Shankar K. Nayak, Khosrow Mahdavi, Cristina de Leon
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 16:47-54
We established short-term cultures of autologous tumors from patients with renal carcinoma for use as active specific immunotherapy (i.e., autologous vaccine).Between 9/91 and 9/99 the cell biology laboratory of the Hoag Cancer Center received 69 kid
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 15:161-168
We have tried to establish short-term cultures of autologous tumors from patients with renal cell carcinoma that could be used as active specific immunotherapy (i.e., autologous vaccine) in such patients after resection of primary kidney cancer, and/
Autor:
Linda D. Beutel, Neil M. Barth, Shankar K. Nayak, Audrey A. O'Connor, Robert O. Dillman, Patric M. Schiltz, S. Robert Hurwitz
Publikováno v:
Cancer Biotherapy and Radiopharmaceuticals. 12:65-71
Adoptive immunotherapy with autologous tumor infiltrating lymphocytes (TIL) is a promising approach for cancer bio-therapy. One issue, however, is whether such cells actually migrate to sites of tumor after intravenous infusion. There have been sever
Publikováno v:
Journal of Immunotherapy. 14:65-69
For active specific immunotherapy, autologous tumor cells grown in vitro may be a more appropriate source of tumor antigen than allogeneic tumor cell lines, autologous tumor cell suspensions, or purified/synthetic tumor antigen. A major limitation to