M. Juweid et al., IMPROVED DETECTION OF MEDULLARY-THYROID CANCER WITH RADIOLABELED ANTIBODIES TO CARCINOEMBRYONIC ANTIGEN, Journal of clinical oncology, 14(4), 1996, pp. 1209-1217
Purpose: This investigation was undertaken to assess the targeting of
established and occult medullary thyroid cancer (MTC) with radiolabele
d monoclonal antibodies (MAbs) reactive with carcinoembryonic antigen
(CEA). Patients and Methods: Twenty-six assessable patients with known
or occult (n = 17) or occult (n = 9) MTC were studied with radiolabel
ed anti-CEA MAbs. Scintigraphic images were collected to determine tar
geting of tumor lesions. Results: The targeting results of technetium
99m (Tc-99m)-, iodine 123 (I-123)-, and iodine 131 (I-131)-labeled ant
i-CEA antibodies (all directed against the same epitope of CEA) indica
ted that all these reagents were capable of detecting established and
occult MTC. The sensitivity for detection of known sites of disease ra
nged from 76% to 100% for the various anti-CEA MAbs used, when compare
d with computed tomography (CT), magnetic resonance imaging (MRI), bon
e scan, or other imaging modalities. Moreover, the antibody scan was p
ositive in seven of nine patients with occult disease (patients with n
egative conventional imaging studies, but who had elevated calcitonin
and/or CEA levels). Three of seven patients underwent surgery and the
disease was confirmed by histopathology in all three. Conclusion: Anti
-CEA MAbs are excellent agents for imaging recurrent, residual, or met
astatic MTC. The high lesion sensitivity in patients with known lesion
s, combined with the ability to detect occult disease, may make these
agents ideal for staging patients, monitoring disease pretherapy or po
sttherapy, and especially for evaluating patients with recurrent or pe
rsistent hypercalcitonemia or CEA elevations after primary surgery. An
alogous to radioiodine in the evaluation of patients with differentiat
ed thyroid cancer, radiolabeled anti-CEA MAbs may achieve a similar ro
le in diagnosing and monitoring patients with MTC. (C) 1996 by America
n Society of Clinical Oncology.