Somatostatin Receptor Antagonists for Imaging and Therapy.

Abstract

Somatostatin receptor (sstr) scintigraphy for imaging and sstr analogs for treatment have been used for more than 20 y. An important improvement in recent years was the introduction of peptide receptor radionuclide therapy with radiolabeled sstr agonists, such as [⁹⁰Y-DOTA⁰,Tyr³]octreotide or [¹⁷⁷Lu-DOTA⁰,Tyr³]octreotide (⁹⁰Y- or ¹⁷⁷Lu-DOTATOC, respectively) and [¹⁷⁷Lu-DOTA⁰,Tyr³]octreotate (¹⁷⁷Lu-DOTATATE). PET/CT with ⁶⁸Ga-labeled sstr agonists, such as ⁶⁸Ga-DOTATOC, ⁶⁸Ga-DOTATATE, and [⁶⁸Ga-DOTA,1-Nal³]octreotide (⁶⁸Ga-DOTANOC), plays an important role in staging and restaging neuroendocrine tumors. Most importantly, sstr scintigraphy and sstr PET/CT can distinguish patients who will qualify for and benefit from peptide receptor radionuclide therapy. This characteristic of sstr targeting is important because it allows a personalized treatment approach (theranostic approach). Until recently, it was thought that internalization of the radiolabeled agonist was mandatory for sstr-mediated imaging and therapy. It was Ginj et al. who proposed in 2006 the paradigm shift that radiolabeled sstr antagonists may perform better than agonists despite the lack of internalization. Despite the rather limited number of head-to-head comparisons of sstr antagonists and agonists, the superiority of sstr antagonists was demonstrated in several cases. From a small library of sstr antagonists, the analog JR11 (Cpa-c[d-Cys-Aph(Hor)-d-Aph(Cbm)-Lys-Thr-Cys]-d-Tyr-NH₂), an antagonist with selectivity for sstr subtype 2, showed the best overall characteristics for sstr subtype 2 targeting and was therefore selected for clinical translation. JR11 is under clinical development as a PET imaging agent when labeled with ⁶⁸Ga (⁶⁸Ga-NODAGA-JR11 or ⁶⁸Ga-OPS202) and as a therapeutic agent when labeled with ¹⁷⁷Lu (¹⁷⁷Lu-DOTA-JR11 or ¹⁷⁷Lu-OPS201). In this article, we discuss the development and current status of radiolabeled sstr antagonists. Evidence based on preclinical work, on quantitative in vivo autoradiography of human tumor slices, and on human data now supports a shift to sstr antagonists.