Department of Medical Oncology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka, 541-8567, Japan.
Int J Clin Oncol. 2024 Sep;29(9):1220-1227. doi: 10.1007/s10147-024-02587-z. Epub 2024 Jul 31.
Human epidermal growth factor receptor 2 has been a pivotal biomarker for gastric cancer treatment strategies for many years. However, more than a decade after the ToGA trial demonstrated the efficacy of trastuzumab in improving survival, the development of treatments targeting human epidermal growth factor receptor 2 remains challenging. Several large-scale clinical trials of tyrosine kinase inhibitors, non-trastuzumab anti-human epidermal growth factor receptor 2 antibodies, and antibody-drug conjugates have failed to meet the primary endpoints. The concept of trastuzumab beyond progression and the complexity of resistance mechanisms to anti-human epidermal growth factor receptor 2 therapy after trastuzumab treatment presented significant obstacles, leading to trastuzumab being the sole therapy for human epidermal growth factor receptor 2-positive gastric cancer for some time. Nevertheless, the landscape has shifted in recent years, especially since the introduction of the antibody-drug conjugate trastuzumab deruxtecan in 2020. This has rekindled the interest in developing treatments targeting human epidermal growth factor receptor 2 in gastric cancer.
人类表皮生长因子受体 2 多年来一直是胃癌治疗策略的重要生物标志物。然而,在 ToGA 试验证明曲妥珠单抗在提高生存率方面的疗效十多年后,针对人类表皮生长因子受体 2 的治疗方法的开发仍然具有挑战性。几种酪氨酸激酶抑制剂、非曲妥珠单抗抗人类表皮生长因子受体 2 抗体和抗体药物偶联物的大型临床试验都未能达到主要终点。曲妥珠单抗耐药后进展和针对人类表皮生长因子受体 2 治疗的耐药机制的复杂性是重大障碍,导致曲妥珠单抗成为一段时间内人类表皮生长因子受体 2 阳性胃癌的唯一治疗方法。然而,近年来情况发生了变化,尤其是 2020 年抗体药物偶联物曲妥珠单抗 deruxtecan 的推出。这重新激起了人们对开发针对胃癌人类表皮生长因子受体 2 的治疗方法的兴趣。