Abstract
Immunoscintigraphy employing radiolabeled monoclonal antibodies (MoAbs) specific for certain selected tumor-associated antigens (TAAs) is becoming increasingly accepted as a routine diagnostic procedure, particularly for staging patients with cancer. In fact, even though the diagnostic potentials of immunoscintigraphy have been explored for diverse applications including cardiovascular diseases (for the detection of thrombi or of damaged myocardial cells), oncology is certainly the field where clinical validation of this new imaging method has been most extensive [for a brief overview on the clinical usefulness of immunoscintigraphy and on some pharmacokinetic aspects concerning this new diagnostic procedure, see Mariani and Strober, 1990]. It is now widely acknowledged that tumor immunoscintigraphy is of great value in terms of both specificity (close to 100%) and sensitivity (about 75–80% on the average). In addition, one of the major advantages of this procedure has been shown to be the ability of detecting distant tumor lesions in about one-third of patients who are apparently “tumor-free” as classified by other, noninvasive diagnostic techniques; therefore, for some specific forms of cancer, immunoscintigraphy may be considered as a mandatory diagnostic procedure for correctly staging and monitoring patients, complementary to other techniques already well established in the clinical routine [Mariani et al., 1989].
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© 1991 Plenum Press, New York
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Mariani, G., Ferrante, L., Rescigno, A. (1991). Pitfalls in Pharmacokinetic Modeling of Monoclonal Antibody Biodistribution in Man. In: Rescigno, A., Thakur, A.K. (eds) New Trends in Pharmacokinetics. NATO ASI Series, vol 221. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8053-5_11
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