Effectiveness of²²⁵Ac-Labeled Anti-EGFR Radioimmunoconjugate in EGFR-Positive Kirsten Rat Sarcoma Viral Oncogene and BRAF Mutant Colorectal Cancer Models

Abstract

Eighty percent of colorectal cancers (CRCs) overexpress epidermal growth factor receptor (EGFR). Kirsten rat sarcoma viral oncogene (KRAS) mutations are present in 40% of CRCs and drive de novo resistance to anti-EGFR drugs. BRAF oncogene is mutated in 7%–10% of CRCs, with even worse prognosis. We have evaluated the effectiveness of [²²⁵Ac]Ac-macropa-nimotuzumab in KRAS mutant and in KRAS wild-type and BRAF^V600E mutant EGFR-positive CRC cells in&nbsp;vitro and in&nbsp;vivo. Anti-CD20 [²²⁵Ac]Ac-macropa-rituximab was developed and used as a nonspecific radioimmunoconjugate. <b>Methods:</b> Anti-EGFR antibody nimotuzumab was radiolabeled with ²²⁵Ac via an 18-membered macrocyclic chelator <i>p</i>-SCN-macropa. The immunoconjugate was characterized using flow cytometry, radioligand binding assay, and high-performance liquid chromatography, and internalization was studied using live-cell imaging. In vitro cytotoxicity was evaluated in 2-dimensional monolayer EGFR-positive KRAS mutant DLD-1, SW620, and SNU-C2B; in KRAS wild-type and BRAF^V600E mutant HT-29 CRC cell lines; and in 3-dimensional spheroids. Dosimetry was studied in healthy mice. The in&nbsp;vivo efficacy of [²²⁵Ac]Ac-macropa-nimotuzumab was evaluated in mice bearing DLD-1, SW620, and HT-29 xenografts after treatment with 3 doses of 13 kBq/dose administered 10 d apart. <b>Results:</b> In all cell lines, in&nbsp;vitro studies showed enhanced cytotoxicity of [²²⁵Ac]Ac-macropa-nimotuzumab compared with nimotuzumab and controls. The inhibitory concentration of 50% in the DLD-1 cell line was 1.8 nM for [²²⁵Ac]Ac-macropa-nimotuzumab versus 84.1 nM for nimotuzumab. Similarly, the inhibitory concentration of 50% was up to 79-fold lower for [²²⁵Ac]Ac-macropa-nimotuzumab than for nimotuzumab in KRAS mutant SNU-C2B and SW620 and in KRAS wild-type and BRAF^V600E mutant HT-29 CRC cell lines. A similar trend was observed for 3-dimensional spheroids. Internalization peaked 24–48 h after incubation and depended on EGFR expression. In the [²²⁵Ac]Ac-macropa-nimotuzumab group, 3 of 7 mice bearing DLD-1 tumors had complete remission. Median survival was 40 and 34 d for mice treated with phosphate-buffered saline and [²²⁵Ac]Ac-macropa-rituximab (control), respectively, whereas it was not reached for the [²²⁵Ac]Ac-macropa-nimotuzumab group (&gt;90 d). Similarly, median survival of mice bearing HT-29 xenografts was 16 and 12.5 d for those treated with [²²⁵Ac]Ac-macropa-rituximab and phosphate-buffered saline, respectively, and was not reached for those treated with [²²⁵Ac]Ac-macropa-nimotuzumab (&gt;90 d). One of 7 mice bearing HT-29 xenografts and treated using [²²⁵Ac]Ac-macropa-nimotuzumab had complete remission. Compared with untreated mice, [²²⁵Ac]Ac-macropa-nimotuzumab more than doubled (16 vs. 41 d) the median survival of mice bearing SW620 xenografts. <b>Conclusion:</b> [²²⁵Ac]Ac-macropa-nimotuzumab is effective against KRAS mutant and BRAF^V600E mutant CRC models.

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