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Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A.
Antibody targeted therapy of cancer results in anti-antibody production which prevents repeated treatment. Cyclosporin A (CsA) has been used to suppress this response in patients treated with a radiolabelled antibody to carcinoembryonic antigen (CEA). Patients with CEA producing tumours received a m...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1988
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246821/ https://www.ncbi.nlm.nih.gov/pubmed/3265333 |
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author | Ledermann, J. A. Begent, R. H. Bagshawe, K. D. Riggs, S. J. Searle, F. Glaser, M. G. Green, A. J. Dale, R. G. |
author_facet | Ledermann, J. A. Begent, R. H. Bagshawe, K. D. Riggs, S. J. Searle, F. Glaser, M. G. Green, A. J. Dale, R. G. |
author_sort | Ledermann, J. A. |
collection | PubMed |
description | Antibody targeted therapy of cancer results in anti-antibody production which prevents repeated treatment. Cyclosporin A (CsA) has been used to suppress this response in patients treated with a radiolabelled antibody to carcinoembryonic antigen (CEA). Patients with CEA producing tumours received a minimum of two courses consisting of an injection of radiolabelled antibody and CsA, 24 mg kg-1 day-1, for 6 days; each course was given at 2 week intervals. Two weeks after the completion of the second course the mean human antimouse antibody (HAMA) levels were 3.5 micrograms ml-1 (s.d. 2.7) in 3 patients receiving CsA and 1,998 micrograms ml-1 (s.d. 387) in 3 patients not receiving the drug. Clearance of antitumour antibody was accelerated and tumour localisation absent when HAMA levels exceeded 30 micrograms ml-1. With lower levels of HAMA in the CsA-treated patients, further antitumour antibody accumulated in the tumour after each dose. Further therapy with antitumour antibody and CsA lead to the development of HAMA, but this was less than 25% of the amount in patients not given CsA. In this preliminary study up to 4 times as many doses of antitumour antibody could be usefully given when CsA was used. This increases the potential for effective antibody targeted therapy of cancer. IMAGES: |
format | Text |
id | pubmed-2246821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22468212009-09-10 Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. Ledermann, J. A. Begent, R. H. Bagshawe, K. D. Riggs, S. J. Searle, F. Glaser, M. G. Green, A. J. Dale, R. G. Br J Cancer Research Article Antibody targeted therapy of cancer results in anti-antibody production which prevents repeated treatment. Cyclosporin A (CsA) has been used to suppress this response in patients treated with a radiolabelled antibody to carcinoembryonic antigen (CEA). Patients with CEA producing tumours received a minimum of two courses consisting of an injection of radiolabelled antibody and CsA, 24 mg kg-1 day-1, for 6 days; each course was given at 2 week intervals. Two weeks after the completion of the second course the mean human antimouse antibody (HAMA) levels were 3.5 micrograms ml-1 (s.d. 2.7) in 3 patients receiving CsA and 1,998 micrograms ml-1 (s.d. 387) in 3 patients not receiving the drug. Clearance of antitumour antibody was accelerated and tumour localisation absent when HAMA levels exceeded 30 micrograms ml-1. With lower levels of HAMA in the CsA-treated patients, further antitumour antibody accumulated in the tumour after each dose. Further therapy with antitumour antibody and CsA lead to the development of HAMA, but this was less than 25% of the amount in patients not given CsA. In this preliminary study up to 4 times as many doses of antitumour antibody could be usefully given when CsA was used. This increases the potential for effective antibody targeted therapy of cancer. IMAGES: Nature Publishing Group 1988-11 /pmc/articles/PMC2246821/ /pubmed/3265333 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Ledermann, J. A. Begent, R. H. Bagshawe, K. D. Riggs, S. J. Searle, F. Glaser, M. G. Green, A. J. Dale, R. G. Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title | Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title_full | Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title_fullStr | Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title_full_unstemmed | Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title_short | Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A. |
title_sort | repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin a. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246821/ https://www.ncbi.nlm.nih.gov/pubmed/3265333 |
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