Regeneron Pharmaceuticals, Inc., Tarrytown, New York.
Cancer Res. 2024 Jul 2;84(13):2169-2180. doi: 10.1158/0008-5472.CAN-23-3195.
The receptor tyrosine kinase FGFR3 is frequently mutated in bladder cancer and is a validated therapeutic target. Although pan-FGFR tyrosine kinase inhibitors (TKI) have shown clinical efficacy, toxicity and acquired resistance limit the benefit of these agents. While antibody-based therapeutics can offer superior selectivity than TKIs, conventional ligand-blocking antibodies are usually ineffective inhibitors of constitutively active receptor tyrosine kinases. Furthermore, the existence of multiple oncogenic variants of FGFR3 presents an additional challenge for antibody-mediated blockade. Here, we developed a tetravalent FGFR3×FGFR3 bispecific antibody that inhibited FGFR3 point mutants and fusion proteins more effectively than any of the conventional FGFR3 antibodies that we produced. Each arm of the bispecific antibody contacted two distinct epitopes of FGFR3 through a cis mode of binding. The antibody blocked dimerization of the most common FGFR3 oncogenic variant (S249C extracellular domain mutation) and inhibited the function of FGFR3 variants that are resistant to pan-FGFR TKIs. The antibody was highly effective in suppressing growth of FGFR3-driven tumor models, providing efficacy comparable to that of the FDA-approved TKI erdafitinib. Thus, this bispecific antibody may provide an effective approach for broad and highly selective inhibition of oncogenic FGFR3 variants. Significance: Development of a bispecific antibody that broadly inhibits gain-of-function FGFR3 variants provides a therapeutic strategy to target tumors with oncogenic FGFR3 point mutations and fusions, a particularly difficult case for antibody blockade.
受体酪氨酸激酶 FGFR3 在膀胱癌中经常发生突变,是经过验证的治疗靶点。虽然泛 FGFR 酪氨酸激酶抑制剂(TKI)已显示出临床疗效,但毒性和获得性耐药限制了这些药物的疗效。虽然基于抗体的治疗方法可以提供比 TKI 更高的选择性,但传统的配体阻断抗体通常对组成性激活的受体酪氨酸激酶无效。此外,FGFR3 的多种致癌变体的存在为抗体介导的阻断提出了额外的挑战。在这里,我们开发了一种四价 FGFR3×FGFR3 双特异性抗体,它比我们生产的任何常规 FGFR3 抗体更有效地抑制 FGFR3 点突变和融合蛋白。双特异性抗体的每个臂通过顺式结合模式与 FGFR3 的两个不同表位接触。该抗体阻断了最常见的 FGFR3 致癌变体(S249C 细胞外结构域突变)的二聚化,并抑制了对泛 FGFR TKI 耐药的 FGFR3 变体的功能。该抗体在抑制 FGFR3 驱动的肿瘤模型的生长方面非常有效,提供的疗效可与 FDA 批准的 TKI 厄达替尼相媲美。因此,这种双特异性抗体可能为广泛且高度选择性抑制致癌 FGFR3 变体提供一种有效的治疗策略。意义:开发一种广泛抑制功能获得性 FGFR3 变体的双特异性抗体为靶向具有致癌 FGFR3 点突变和融合的肿瘤提供了一种治疗策略,这对抗体阻断来说是一个特别困难的情况。