Back to Search Start Over

Therapeutic efficacy of α-radioimmunotherapy with different activity levels of the 213 Bi-labeled monoclonal antibody MX35 in an ovarian cancer model.

Authors :
Gustafsson-Lutz A
Bäck T
Aneheim E
Hultborn R
Palm S
Jacobsson L
Morgenstern A
Bruchertseifer F
Albertsson P
Lindegren S
Source :
EJNMMI research [EJNMMI Res] 2017 Dec; Vol. 7 (1), pp. 38. Date of Electronic Publication: 2017 Apr 24.
Publication Year :
2017

Abstract

Background: The aim of this study was to compare the therapeutic efficacy of two different activity levels of the <superscript>213</superscript> Bi-labeled monoclonal antibody MX35 in an ovarian cancer model. Sixty female BALB/c (nu/nu) mice were inoculated intraperitoneally with human ovarian cancer cells (OVCAR-3). Two weeks later, 40 mice were injected intraperitoneal (i.p.) with 1 ml of <superscript>213</superscript> Bi-MX35, 3 MBq/mL (n = 20), or 9 MBq/mL (n = 20). An additional 20 mice received unlabeled MX35. Incidence of tumors and ascites was investigated 8 weeks after therapy. Body weight and white blood cell counts were monitored after treatment for possible signs of toxicity.<br />Results: The tumor-free fraction of the animals treated with 3 MBq/mL of <superscript>213</superscript> Bi-MX35 was 0.55, whereas that of animals treated with 9 MBq/mL of <superscript>213</superscript> Bi-MX35 was 0.78. The control group treated with unlabeled MX35 had a tumor-free fraction of 0.15. No significant reduction in white blood cell counts or weight loss was observed.<br />Conclusions: Tumor growth after i.p. treatment with <superscript>213</superscript> Bi-MX35 was significantly reduced compared to treatment with unlabeled MX35. Treatment with 9 MBq/mL of <superscript>213</superscript> Bi-MX35 resulted in higher tumor-free fraction compared with 3 MBq/mL of <superscript>213</superscript> Bi-MX35, but this difference was not statistically significant. No signs of toxicity were observed in the treated animals.

Details

Language :
English
ISSN :
2191-219X
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
EJNMMI research
Publication Type :
Academic Journal
Accession number :
28439844
Full Text :
https://doi.org/10.1186/s13550-017-0283-2