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Receptor radionuclide therapy with 90Y-[DOTA]0-Tyr3-octreotide (90Y-DOTATOC) in neuroendocrine tumours

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Abstract

Somatostatin receptors are over-expressed in many tumours, mainly of neuroendocrine origin, thus enabling treatment with somatostatin analogues. Almost a decade of clinical experience of receptor radionuclide therapy with the analogue 90Y-[DOTA]0-Tyr3-octreotide [90Y-DOTATOC] has now been obtained at a few centres of excellence. This review reports on the present state of the art of receptor radionuclide therapy and discusses new perspectives.

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Acknowledgements

The authors thank Daria Handkiewicz-Junak, Maribel Lopera Sierra, Helmut R Mäcke and Filippo de Braud for their invaluable help in the preparation of this manuscript. The authors thank William Russell-Edu for his kind assistance in revising the English of this manuscript and Mrs. Deborah Console for the editing. This work was supported by grants from the Italian Association for Cancer Research (AIRC), the Italian National Council for Research (PSO CNR-MIUR) and the Italian Ministry of Health.

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Correspondence to Giovanni Paganelli.

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Bodei, L., Cremonesi, M., Grana, C. et al. Receptor radionuclide therapy with 90Y-[DOTA]0-Tyr3-octreotide (90Y-DOTATOC) in neuroendocrine tumours. Eur J Nucl Med Mol Imaging 31, 1038–1046 (2004). https://doi.org/10.1007/s00259-004-1571-4

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