National Cancer Center Hospital East, Kashiwa, Japan.
Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nat Med. 2024 Jul;30(7):1933-1942. doi: 10.1038/s41591-024-02992-x. Epub 2024 May 14.
Trastuzumab deruxtecan (T-DXd) showed statistically significant clinical improvement in patients with human epidermal growth factor receptor 2-positive (HER2) gastric cancer in the DESTINY-Gastric01 trial. Exploratory results from DESTINY-Gastric01 suggested a potential benefit in patients with HER2-low gastric cancer. Spatial and temporal heterogeneity in HER2 expression or gene alteration, an inherent characteristic of gastric cancer tumors, presents a challenge in identifying patients who may respond to T-DXd. Specific biomarkers related to therapeutic response have not been explored extensively. Exploratory analyses were conducted to assess baseline HER2-associated biomarkers in circulating tumor DNA and tissue samples, and to investigate mechanisms of resistance to T-DXd. Baseline HER2-associated biomarkers were correlated with objective response rate (ORR) in the primary cohort of patients with HER2 gastric cancer. The primary cohort had 64% concordance between HER2 positivity and HER2 (ERBB2) plasma gene amplification. Other key driver gene amplifications, specifically MET, EGFR and FGFR2, in circulating tumor DNA were associated with numerically lower ORR. Among 12 patients with HER2 gain-of-function mutations, ORR was 58.3% (7 of 12). ORR was consistent regardless of timing of immunohistochemistry sample collection. Further investigations are required in larger studies.
在 DESTINY-Gastric01 试验中,曲妥珠单抗-德鲁替康(T-DXd)在人表皮生长因子受体 2 阳性(HER2)胃癌患者中显示出具有统计学意义的临床改善。DESTINY-Gastric01 的探索性结果表明,HER2 低表达胃癌患者可能从中获益。HER2 表达或基因改变的空间和时间异质性是胃癌肿瘤的固有特征,这给识别可能对 T-DXd 有反应的患者带来了挑战。与治疗反应相关的特定生物标志物尚未得到广泛探索。进行了探索性分析,以评估循环肿瘤 DNA 和组织样本中基线 HER2 相关生物标志物,并研究对 T-DXd 耐药的机制。基线 HER2 相关生物标志物与 HER2 阳性胃癌患者的主要队列的客观缓解率(ORR)相关。主要队列中 HER2 阳性与 HER2(ERBB2)血浆基因扩增的一致性为 64%。循环肿瘤 DNA 中其他关键驱动基因扩增,特别是 MET、EGFR 和 FGFR2,与较低的 ORR 相关。在 12 名 HER2 功能获得性突变患者中,ORR 为 58.3%(12 名中有 7 名)。无论免疫组织化学样本采集的时间如何,ORR 都是一致的。需要在更大的研究中进一步研究。