|
Cancer Biotherapy & Radiopharmaceuticals
Pharmacokinetics, Biodistribution, and Radioimmunotherapy with Monoclonal Antibody 776.1 in a Murine Model of Human Ovarian Cancer
To cite this article:
Marc A. Berger, Gregg R. Masters, Judith Singleton, Michael S. Scully, Lisa G. Grimm, Daniel A. Soltis, Earl F. Albone, .
Cancer Biotherapy & Radiopharmaceuticals.
December 2005,
20(6): 589-602.
doi:10.1089/cbr.2005.20.589.
Marc A. Berger Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Gregg R. Masters Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Judith Singleton Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Michael S. Scully Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Lisa G. Grimm Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Daniel A. Soltis Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Earl F. Albone Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ. Purdue Pharma, L.P., Immunotherapeutics Department, Cranbury, NJ 776.1 is a murine IgG1 monoclonal antibody to the human ovarian cancer antigen CA 125 that has the unique property of having a clear preference for binding to the cell-associated form of the antigen. We have examined the tumor localization properties and efficacy of 776.1 in a subcutaneous OVCAR-3 xenograft mouse model of human ovarian cancer. Biodistribution experiments using 125I-labeled 776.1 demonstrated a peak uptake in tumors at 72 hours postinjection, with an average of 17.7% of injected dose per gram localized to the tumor. Little uptake in other organs was observed. Further experiments using CA 125-transfected syngeneic tumors, as well as an immunoprecipitation assay using human chimeric 776.1, both clearly demonstrated that 776.1 localizes to the tumor in a CA 125-dependent manner. DOTA-776.1 (1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″ tetraacetic acid-conjugated 776.1) was labeled with 90Y and used in efficacy studies. [90Y-DOTA]776.1 at a single dose of 150 µCi was able to mediate efficient reduction of tumor growth, with regression observed in a subset of animals for a period ranging from 3 to 48 days, equivalent to 3 weekly administrations of cisplatin at 6 mg/kg. No significant regression was observed in groups receiving [90Y-DOTA]MOPC-21 control antibody at any dose. These results suggest that 776.1 may be a promising radioimmunotherapeutic agent for the treatment of human ovarian cancer.  This paper was cited by:Radioimmunotherapy of solid tumors targeting a cell-surface protein, FZD10: therapeutic efficacy largely depends on radiosensitivity Hirofumi Hanaoka, Toyomasa Katagiri, Chikako Fukukawa, Hiroki Yoshioka, Shinji Yamamoto, Yasuhiko Iida, Tetsuya Higuchi, Noboru Oriuchi, Bishnuhari Paudyal, Pramila Paudyal, Yusuke Nakamura, Keigo Endo Annals of Nuclear Medicine. Aug 2009, Vol. 23, No. 5: 479-485 CrossRef Bioevaluation studies of 32P incorporated mould brachytherapy sources for potential application in treatment of superficial tumors Usha Pandey, Sanjay Kumar Saxena, Haladhar Dev Sarma, Pankaj Tandon, Ramu Ram, Grace Samuel, Ashutosh Dash, Meera Venkatesh Nuclear Medicine Communications. Sep 2008, Vol. 29, No. 8: 717-723 CrossRef
|
|