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Biologic response modifiers in gynecologic malignancies.

Biological therapy is currently being investigated in the treatment of a number of malignancies. The hypothesis for the use of this therapeutic modality involves an attempt to stimulate an already existent but perhaps suboptimal immune response to foreign protein, including tumor. Immunologic therap...

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Detalles Bibliográficos
Autores principales: Dutcher, J. P., Wadler, S., Wiernik, P. H.
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590271/
https://www.ncbi.nlm.nih.gov/pubmed/2461003
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author Dutcher, J. P.
Wadler, S.
Wiernik, P. H.
author_facet Dutcher, J. P.
Wadler, S.
Wiernik, P. H.
author_sort Dutcher, J. P.
collection PubMed
description Biological therapy is currently being investigated in the treatment of a number of malignancies. The hypothesis for the use of this therapeutic modality involves an attempt to stimulate an already existent but perhaps suboptimal immune response to foreign protein, including tumor. Immunologic therapy appears to work best against small-volume disease, as indicated from animal studies. This condition is potentially achievable in advanced ovarian cancer, where surgery is capable of producing multi-log reduction in tumor mass, and thus immunotherapy may be an option in this disease. The attraction of biologic therapy in patients with ovarian cancer is the potential to treat relatively localized but often chemotherapy-resistant disease. In cervical cancer, the rationale for the use of interferon is somewhat different in that this disease may be a manifestation of a virally induced proliferative lesion. Thus, the antiviral properties of interferon are being investigated in both limited and advanced cervical cancer. Both of these hypothesis have pre-clinical data to support them. This paper presents the pre-clinical and clinical work currently available for consideration of future use.
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spelling pubmed-25902712008-11-28 Biologic response modifiers in gynecologic malignancies. Dutcher, J. P. Wadler, S. Wiernik, P. H. Yale J Biol Med Research Article Biological therapy is currently being investigated in the treatment of a number of malignancies. The hypothesis for the use of this therapeutic modality involves an attempt to stimulate an already existent but perhaps suboptimal immune response to foreign protein, including tumor. Immunologic therapy appears to work best against small-volume disease, as indicated from animal studies. This condition is potentially achievable in advanced ovarian cancer, where surgery is capable of producing multi-log reduction in tumor mass, and thus immunotherapy may be an option in this disease. The attraction of biologic therapy in patients with ovarian cancer is the potential to treat relatively localized but often chemotherapy-resistant disease. In cervical cancer, the rationale for the use of interferon is somewhat different in that this disease may be a manifestation of a virally induced proliferative lesion. Thus, the antiviral properties of interferon are being investigated in both limited and advanced cervical cancer. Both of these hypothesis have pre-clinical data to support them. This paper presents the pre-clinical and clinical work currently available for consideration of future use. Yale Journal of Biology and Medicine 1988 /pmc/articles/PMC2590271/ /pubmed/2461003 Text en
spellingShingle Research Article
Dutcher, J. P.
Wadler, S.
Wiernik, P. H.
Biologic response modifiers in gynecologic malignancies.
title Biologic response modifiers in gynecologic malignancies.
title_full Biologic response modifiers in gynecologic malignancies.
title_fullStr Biologic response modifiers in gynecologic malignancies.
title_full_unstemmed Biologic response modifiers in gynecologic malignancies.
title_short Biologic response modifiers in gynecologic malignancies.
title_sort biologic response modifiers in gynecologic malignancies.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590271/
https://www.ncbi.nlm.nih.gov/pubmed/2461003
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