Targeted Radionuclide Therapy with A 177Lu-labeled Anti-HER2 Nanobody

RIT has become an attractive strategy in cancer treatment, but still faces important drawbacks due to poor tumor penetration and undesirable pharmacokinetics of the targeting vehicles.Smaller radiolabeled antibody fragments and peptides feature highly specific target accumulation, resulting in low accumulation in healthy tissue, except for the kidneys.Nanobodies are the smallest (MW < 15 kDa) functional antigen-binding fragments that are derived from heavy chain-only camelid antibodies.Here, we show that the extend of kidney retention of nanobodies is predominantly dictated by the number of polar residues in the C-terminal amino acid tag.Three nanobodies were produced with different C-terminal amino-acid tag sequences (Myc-His-tagged, His-tagged, and untagged).Dynamic planar imaging of Wistar rats with 111 In-DTPA-nanobodies revealed that untagged nanobodies showed a 70 % drop in kidney accumulation compared to Myc-His-tagged nanobodies at 50 min p.i..In addition, coinfusion of untagged nanobodies with the plasma expander Gelofusin led to a final reduction of 90 %.Similar findings were obtained with different 177 Lu-DTPA-2Rs15d nanobody constructs in HER2 pos tumor xenografted mice at 1 h p.i.. Kidney accumulation decreased 88 % when comparing Myc-His-tagged to untagged 2Rs15d nanobody, and 95 % with a coinfusion of Gelofusin, without affecting the tumor targeting capacity.Consequently, we identified a generic method to reduce kidney retention of radiolabeled nanobodies.Dosimetry calculations of Gelofusin-coinfused, untagged 177 Lu-DTPA-2Rs15d revealed a dose of 0.90 Gy/MBq that was delivered to both tumor and kidneys and extremely low doses to healthy tissues.In a comparative study, 177 Lu-DTPA-Trastuzumab supplied 6 times more radiation to the tumor than untagged 177 Lu-DTPA-2Rs15d, but concomitantly also a 155, 34, 80, 26 and 4180 fold higher radioactivity burden to lung, liver, spleen, bone and blood.Most importantly, nanobody-based targeted radionuclide therapy in mice bearing small estiblashed HER2 pos tumors led to an almost complete blockade of tumor growth and a significant difference in event-free survival between the treated and the control groups (P < 0.0001).Based on histology analyses, no evidence of renal inflammation, apoptosis or necrosis was obtained. Ivyspring International