Radioimmunotherapy with 90Y-Labeled Monoclonal Antibodies in a Nude Mouse Ovarian Cancer Model

Authors

  • Kalevi Kairemo Departments of Clinical Chemistry and Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki
  • Kaj Ljunggren Department of Radiation Physics, University of Lund, Lund, Sweden
  • Sven-Erik Strand Departments of Clinical Chemistry and Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki
  • Jukka Hiltunen MAP Medical Technologies, Jyväskylä, and Cancer Research Laboratory, Orion/Farmos-Group Ltd., Turku, Finland
  • Pirkko Penttilä MAP Medical Technologies, Jyväskylä, and Cancer Research Laboratory, Orion/Farmos-Group Ltd., Turku, Finland
  • Tuomo Nikula MAP Medical Technologies, Jyväskylä, and Cancer Research Laboratory, Orion/Farmos-Group Ltd., Turku, Finland
  • Aire Laine MAP Medical Technologies, Jyväskylä, and Cancer Research Laboratory, Orion/Farmos-Group Ltd., Turku, Finland
  • Torsten Wahlström Departments of Clinical Chemistry and Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki

DOI:

https://doi.org/10.3109/02841869309096139

Abstract

Tumor stroma contains much fibrin, and so monoclonal antifibrin antibody can accumulate in tumors. We treated nude mice bearing human ovarian carcinoma xenografts with 90Y-labeled monoclonal antifibrin antibody Fab fragments administered intratumorally. The survival time vs. a control group was significantly prolonged and tumor growth rate was decreased. Another group of animals was treated with 90Y-labeled OC 125-monoclonal antibody; these mice received the antibodies intratumorally, intraperitoneally or intravenously. The survival time was longest in the intratumorally treated group. There was no significant difference in survival between 90Y-labeled OC 125 and antifibrin in the intratumorally treated animal groups. The tissue activity distribution studies revealed that bone marrow is the critical organ. Intratumorally injected monoclonal 90Y-antifibrin antibodies were retained at least 36h (up to 50% of injected activity per gram tumor tissue) in the xenograft after one treatment, causing cell death. Beta-camera imaging and immunohistochemistry were performed for studies of the correlation between 90Y activity and fibrin distribution in tumor specimens. These results were in concordance. In conclusion, intratumoral administration seems suitable for radioimmunotherapy, with an antibody that targets stromal structures. The accumulation can be successfully monitored by a beta-camera.

Downloads

Download data is not yet available.

Downloads

Published

1993-01-01

How to Cite

Kairemo, K. ., Ljunggren, K. ., Strand, S.-E. ., Hiltunen, J. ., Penttilä, P. ., Nikula, T. ., … Wahlström, T. . (1993). Radioimmunotherapy with 90Y-Labeled Monoclonal Antibodies in a Nude Mouse Ovarian Cancer Model. Acta Oncologica, 32(7-8), 801–805. https://doi.org/10.3109/02841869309096139