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Departments of Nuclear Medicine and Surgery, Institute of Biochemistry, University of Lausanne, Lausanne; Division of Radiopharmacy, Paul Scherrer Institute, Villigen, Switzerland
Correspondence: For correspondence or reprints contact: Angelika Bischof Delaloye, MD, Nuclear Medicine Department, Centre Hospitalier Universitaire Vaudois, CH-1011 Lausanne, Switzerland.
ABSTRACT
Copper-67 has comparable beta-particle emissions to that of 131I, but it displays more favorable gamma emission characteristics for application in radioimmunotherapy (RIT). This study investigates the potential of 67C-labeled monoclonal antibody (MAb) 35 for RIT of colorectal carcinoma. Methods: Biokinetics of simultaneously injected 67C- and 125I-labeled MAb35 were studied in six patients scheduled for surgery of primary colorectal cancer. Results: Whole-body clearance (T1/2)of 67C, estimated from sequential anterior and posterior whole-body scans and corrected for decay of 67C, was 41 hr. Serum clearance of 67C was faster (27.41 hr) than that of 125I(38.33 hr). Mean tumor uptake of the 67C-labeled compound (0.0133 %ID/g) exceeded that of 125I(0.0095 %ID/g), and tumor-to-blood ratios were higher for 67C than for 125I, with averages of 6.07 and 2.41, respectively. The average 67C/125I ratio was 1.9 for tumor uptake, 0.7 for blood and 2.6 for tumor-to-blood ratios. Nonspecific liver uptake of 67C as calculated from whole-body scans was high in four patients, up to 25% of residual whole-body activity at 48 hr, but did not increase with time. We also observed some nonspecific bowel activity, as well as moderate to high uptake in benign polyps. Conclusion: Copper-67-labeled MAb35 is more favorable than its radioiodine-labeled counterpart for RIT of colorectal carcinoma due to higher tumor-to-blood ratios, but the problem of nonspecific liver and bowel uptake must first be overcome. The absolute accumulation of activity in tumor remains low, however, so the probability of cure with this compound alone is questionable. The use of 67C as one component of a multimodality adjuvant treatment seems to remain the most appropriate application for RIT.
Key Words: anti-CEA monoclonal antibodies radioimmunotherapy copper-67 iodine-125 colorectal carcinoma
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