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Journal of Nuclear Medicine Vol. 44 No. 5 700-707
© 2003 by Society of Nuclear Medicine


Clinical Investigations

Evaluation of 111In-DTPA-Folate as a Receptor-Targeted Diagnostic Agent for Ovarian Cancer: Initial Clinical Results

Barry A. Siegel, MD1,2, Farrokh Dehdashti, MD1,2, David G. Mutch, MD2,3, Donald A. Podoloff, MD4, Richard Wendt, PhD4, Gregory P. Sutton, MD5, Robert W. Burt, MD6, P. Ron Ellis, MBA7, Carla J. Mathias, BA8, Mark A. Green, PhD8 and David M. Gershenson, MD9

1 Division of Nuclear Medicine, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri
2 Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri
3 Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, Missouri
4 Department of Nuclear Medicine, University of Texas M.D. Anderson Cancer Center, Houston, Texas
5 Department of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, Indiana
6 Department of Radiology, Veterans Affairs Medical Center, Indianapolis, Indiana
7 Endocyte, Inc., West Lafayette, Indiana
8 Division of Nuclear Pharmacy, Department of Industrial and Physical Pharmacy, Purdue University, West Lafayette, Indiana
9 Department of Gynecologic Oncology, University of Texas M.D. Anderson Cancer Center, Houston, Texas

The cell-membrane folate receptor is a potential molecular target for tumor-selective drug delivery, including radiolabeled folate-chelate conjugates for diagnostic imaging. We report here the initial clinical study of such an agent, 111In-diethylenetriaminepentaacetic acid (DTPA)-folate, evaluated for diagnosis of ovarian malignancy. Methods: Thirty-five women were enrolled in a phase I/II clinical study, with 33 completing the surgical follow-up required by the study protocol for definition of disease status. Patients either had a pathologically proven malignancy or were scheduled for surgery for suspected new ovarian cancer (n = 26), recurrent ovarian cancer (n = 5), or endometrial cancer (n = 2). 111In-DTPA-folate was administered as an intravenous bolus, and whole-body images were obtained at 30 min, 4 h, and (for the first 19 patients) 24 h after injection; SPECT also was done at the delayed imaging times. For 19 of the patients, unlabeled free folic acid was injected before administration of 111In-DTPA-folate to also assess the impact of folate loading on tracer biodistribution. Masked and unmasked readings of the images by 2 nuclear medicine physicians were compared with the pathologic findings after surgery. Results: Among 33 patients who had surgical intervention, 14 had new or recurrent malignant tumors. All of 7 newly diagnosed ovarian carcinomas were identified by both masked readers (sensitivity, 100%). The sensitivity for detection of 7 recurrent malignancies was 38% for masked readings and 85% for unmasked readings, indicating that correlation with anatomic imaging studies (CT) was highly important in diagnosis of these lesions. Eighteen of the studied patients were found to have benign masses; for this limited population, the specificity of 111In-DTPA-folate scintigraphy was 76% and 82% for the masked and unmasked analyses, respectively. Conclusion: 111In-DTPA-folate is safe, and possibly effective, for scintigraphy differentiating between malignant and benign ovarian masses.

Key Words: folate receptor • tumor imaging • 111In • ovarian carcinoma




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