Ovarian cancer is a highly malignant tumor of mainly postmenopausal women. The long-term prognosis of this malignancy is largely determined by micrometastasis present at the time of second-look surgery. In general, patients face a poor outcome. New radio-immunoscintigraphic methods to target tumor t
Antibody-antigen complex formation following injection of OC125 monoclonal antibody in patients with ovarian cancer
β Scribed by Hidde J. Haisma; Anne Battaile; Earl W. Stradtman; Robert C. Knapp; Vincent R. Zurawski Jr.
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- French
- Weight
- 553 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Monoclonal antibody (MAb) O C 125 binds to approximately 80% of epithelial ovarian cancers. Serum antigen, CAI25, can be detected in these patients. "'I-OC 125-F(ab')2 was injected into 5 ovarian carcinoma patients with preinjection serum levels of I50 to 9,000 CAI25 U/ml. Patients received the antibody intravenously in doses ranging from 0.46 to 0.94 mg with a specific activity of approximately 2.5 mCilmg '"I. The halflife in the circulation was approximately 30 hr and was independent of serum CAI25 levels. Clearance of "'I from the circulation fitted an open, one-compartment mathematical model. Gel filtration chromatography revealed antibody-antigen complexes in sera 15 min after injection of the radiolabelled antibody. By 5 days after injection, the free form of OC125 antibody could not be detected in the serum. The rate of complex formation correlated well with the observed preinjection serum CA 125 levels. This direct correlation was verified in vitro using purified CAI25 antigen and radiolabelled OC125 F(ab')2 fragments. The specific effects of complex formation on tumor localization remains unclear. However, the presence of complexes should not be ignored, when planning for diagnostic imaging or immunotherapy with OCl25 or other MAbs reacting with circulating antigen.
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