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Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice
The aim of this study was to investigate the therapeutic efficacy of α-radioimmunotherapy of ovarian cancer in mice using different fractionated treatment regimens. The study was performed using the monoclonal antibody MX35 F(ab′)(2) labeled with the α-particle emitter (211)At. Methods. Nude mice we...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766502/ https://www.ncbi.nlm.nih.gov/pubmed/19859581 http://dx.doi.org/10.1155/2010/394913 |
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author | Elgqvist, Jörgen Andersson, Håkan Jensen, Holger Kahu, Helena Lindegren, Sture Warnhammar, Elisabet Hultborn, Ragnar |
author_facet | Elgqvist, Jörgen Andersson, Håkan Jensen, Holger Kahu, Helena Lindegren, Sture Warnhammar, Elisabet Hultborn, Ragnar |
author_sort | Elgqvist, Jörgen |
collection | PubMed |
description | The aim of this study was to investigate the therapeutic efficacy of α-radioimmunotherapy of ovarian cancer in mice using different fractionated treatment regimens. The study was performed using the monoclonal antibody MX35 F(ab′)(2) labeled with the α-particle emitter (211)At. Methods. Nude mice were intraperitoneally inoculated with ~1 × 10(7) cells of the cell line NIH:OVCAR-3. Four weeks later 6 groups of animals were given 400 kBq (211)At-MX35 F(ab′)(2) as a single or as a repeated treatment of up to 6 times (n = 18 in each group). The fractionated treatments were given every seventh day. Control animals were treated with unlabeled MX35 F(ab′)(2) (n = 12). Eight weeks posttreatment the animals were sacrificed and the presence of macro- and microscopic tumors and ascites was determined. Results. The tumor-free fractions (TFFs) of the animals, defined as the fraction of animals with no macro- and microtumors and no ascites, were 0.17, 0.11, 0.39, 0.44, 0.44, and 0.67 when treated with 400 kBq (211)At-MX35 F(ab′)(2) once or 2, 3, 4, 5, or 6 times, respectively. Repeated treatment 3 times or more resulted in a significantly higher (P < .05) TFF than compared to treatment once or twice. The presence of ascites decreased from 15 out of 18 animals in the group given only one treatment to zero for the 2 groups given 5 or 6 fractions. Treatment with unlabeled MX35 F(ab′)(2) resulted in a TFF of zero. Conclusion. Weekly repeated intraperitoneal injections of tolerable amounts of activity of (211)At-MX35 F(ab′)(2) of up to 6 times produced increased therapeutic efficacy without observed toxicity, indicating a potential increase of the therapeutic index. |
format | Text |
id | pubmed-2766502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-27665022009-10-26 Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice Elgqvist, Jörgen Andersson, Håkan Jensen, Holger Kahu, Helena Lindegren, Sture Warnhammar, Elisabet Hultborn, Ragnar J Oncol Research Article The aim of this study was to investigate the therapeutic efficacy of α-radioimmunotherapy of ovarian cancer in mice using different fractionated treatment regimens. The study was performed using the monoclonal antibody MX35 F(ab′)(2) labeled with the α-particle emitter (211)At. Methods. Nude mice were intraperitoneally inoculated with ~1 × 10(7) cells of the cell line NIH:OVCAR-3. Four weeks later 6 groups of animals were given 400 kBq (211)At-MX35 F(ab′)(2) as a single or as a repeated treatment of up to 6 times (n = 18 in each group). The fractionated treatments were given every seventh day. Control animals were treated with unlabeled MX35 F(ab′)(2) (n = 12). Eight weeks posttreatment the animals were sacrificed and the presence of macro- and microscopic tumors and ascites was determined. Results. The tumor-free fractions (TFFs) of the animals, defined as the fraction of animals with no macro- and microtumors and no ascites, were 0.17, 0.11, 0.39, 0.44, 0.44, and 0.67 when treated with 400 kBq (211)At-MX35 F(ab′)(2) once or 2, 3, 4, 5, or 6 times, respectively. Repeated treatment 3 times or more resulted in a significantly higher (P < .05) TFF than compared to treatment once or twice. The presence of ascites decreased from 15 out of 18 animals in the group given only one treatment to zero for the 2 groups given 5 or 6 fractions. Treatment with unlabeled MX35 F(ab′)(2) resulted in a TFF of zero. Conclusion. Weekly repeated intraperitoneal injections of tolerable amounts of activity of (211)At-MX35 F(ab′)(2) of up to 6 times produced increased therapeutic efficacy without observed toxicity, indicating a potential increase of the therapeutic index. Hindawi Publishing Corporation 2010 2009-10-25 /pmc/articles/PMC2766502/ /pubmed/19859581 http://dx.doi.org/10.1155/2010/394913 Text en Copyright © 2010 Jörgen Elgqvist et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Elgqvist, Jörgen Andersson, Håkan Jensen, Holger Kahu, Helena Lindegren, Sture Warnhammar, Elisabet Hultborn, Ragnar Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title | Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title_full | Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title_fullStr | Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title_full_unstemmed | Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title_short | Repeated Intraperitoneal α-Radioimmunotherapy of Ovarian Cancer in Mice |
title_sort | repeated intraperitoneal α-radioimmunotherapy of ovarian cancer in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766502/ https://www.ncbi.nlm.nih.gov/pubmed/19859581 http://dx.doi.org/10.1155/2010/394913 |
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