Dissemin is shutting down on January 1st, 2025

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Elsevier, European Journal of Cancer, 13(49), p. 2851-2858, 2013

DOI: 10.1016/j.ejca.2013.04.009

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The strength of small: Improved targeting of Insulin-like Growth Factor-1 Receptor (IGF-1R) with F(ab')2-R1507 fragments in Ewing sarcomas

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

PURPOSE: To investigate whether F(ab')2-fragments of the monoclonal Insulin-like Growth Factor-1 Receptor (IGF-1R) antibody R1507 (F(ab')2-R1507) can successfully target IGF-1R in Ewing sarcomas (ES). MATERIALS AND METHODS: BALB/c nude mice were subcutaneously implanted with IGF-1R-expressing human ES xenografts (EW-5 and EW-8) which previously showed heterogeneous or no uptake of indium-111-labelled R1507 IgG ((111)In-R1507), respectively. Mice were injected with (111)In-F(ab')2-R1507 or (111)In-R1507 as a reference. Biodistribution and immuno-SPECT/computed tomography (CT) imaging studies were carried out 2, 4, 8 and 24h post-injection (p.i.) for (111)In-F(ab')2-R1507 and 24h p.i. for (111)In-R1507. RESULTS: Biodistribution studies showed specific accumulation of (111)In-F(ab')2-R1507 in EW-5 xenografts from t=2h p.i. onwards (3.6+/-0.2%ID/g at t=24h p.i.) and (111)In-F(ab')2-R1507 immuno-SPECT showed almost homogeneous intratumoural distribution at t=24h p.i. Tumour-to-blood ratios of (111)In-F(ab')2-R1507 were significantly higher than those of (111)In-R1507 at t=24h p.i. (2.4+/-0.4 versus 0.5+/-0.1, respectively; p