Receptor Targeting for Tumor Localisation and Therapy with Radiopeptides

Title: Receptor Targeting for Tumor Localisation and Therapy with Radiopeptides

Volume: 7 Issue: 9

Author(s): A. Heppeler, S. Froidevaux, A. N. Eberle and H. R. Maecke

Affiliation:

Keywords: radiopeptides, melanocyte stimulating hormone MSH, neurotensin, vasoactive, tetraazacyclododecane 1 4 7 10 tetraacetic acid DOTA, D phe 1 octerotide DOTAOC D Phe1 Tyr3, vapreotide DITAVAP, lanreodtide DOTALAN, positron emission tomography PET, radioiodiantion fluorination, diethylenetriaminepentacetic acid DTPA, bifunctional chelating BFCs, melanocyte stimulating hormonev, vasoactive intestinal peptide, subtance P, cholecystokinin B gastrin, bombesin

Abstract: Receptor targeting with radiolabeled peptides has become very important in nuclear oncology in the past few years. The most frequently used peptides in the clinic are analogs of somatostatin (SRIF), e.g. OctreoScan, which contain chelators for the radioisotopes 111 In, 86Y, 90 Y, 67Ga, 68Ga and 64Cu or for 99m Tc and 188Re. and were labelled with the halogens 123I and 18F. Radiolabeled analogs of a-melanocyte-stimulating hormone (a-MSH), neurotensin, vasoactive intestinal peptide (VIP), bombesin (BN), substance P (SP) and gastrin/cholecystokinin (CCK) are also being developed, evaluated in vitro and in vivo and tested for clinical application. This review focuses on the expression in tumors and the regulation of receptors for these neuropeptides as well as the development of novel chelator-peptide conjugates suitable for in vivo scintigraphy or internal radiotherapy. The state of the art of radiopeptide pharmaceuticals is illustrated with four SRIF analogs, modified with the macrocyclic chelator 1, 4, 7, 10-tetraazacyclododecane- 1, 4, 7, 10-tetraacetic acid (DOTA) (D-Phe 1 )-octreotide (DOTAOC), [D-Phe 1 , Tyr 3 )-octreotide (DOTATOC), vapreotide (DOTAVAP) and lanreotide (DOTALAN). DOTA is almost a universal chelator capable of strongly encapsulating hard metals such as 111 In and 67 Ga for Single Photon Emission Tomography (SPET), 68 Ga, 86 Y and 64 Cu for Positron Emission Tomography (PET) as well as 90 Y for receptor-mediated radionuclide therapy and radiolanthanides which exhibit different interesting decay schemes. From biodistribution studies in experimental animals and from clinical data it is concluded that DOTATOC is currently the most suitable SRIF radiopeptide with the best potential in the clinic.

Cite this article as:

Heppeler A., Froidevaux S., Eberle N. A. and Maecke R. H., Receptor Targeting for Tumor Localisation and Therapy with Radiopeptides, Current Medicinal Chemistry 2000; 7 (9) . https://dx.doi.org/10.2174/0929867003374516