INSERM U981, Gustave Roussy, Villejuif, France.
Department of Medical Oncology, Gustave Roussy, Villejuif, France.
Nat Med. 2023 Aug;29(8):2110-2120. doi: 10.1038/s41591-023-02478-2. Epub 2023 Jul 24.
The mechanisms of action of and resistance to trastuzumab deruxtecan (T-DXd), an anti-HER2-drug conjugate for breast cancer treatment, remain unclear. The phase 2 DAISY trial evaluated the efficacy of T-DXd in patients with HER2-overexpressing (n = 72, cohort 1), HER2-low (n = 74, cohort 2) and HER2 non-expressing (n = 40, cohort 3) metastatic breast cancer. In the full analysis set population (n = 177), the confirmed objective response rate (primary endpoint) was 70.6% (95% confidence interval (CI) 58.3-81) in cohort 1, 37.5% (95% CI 26.4-49.7) in cohort 2 and 29.7% (95% CI 15.9-47) in cohort 3. The primary endpoint was met in cohorts 1 and 2. Secondary endpoints included safety. No new safety signals were observed. During treatment, HER2-expressing tumors (n = 4) presented strong T-DXd staining. Conversely, HER2 immunohistochemistry 0 samples (n = 3) presented no or very few T-DXd staining (Pearson correlation coefficient r = 0.75, P = 0.053). Among patients with HER2 immunohistochemistry 0 metastatic breast cancer, 5 of 14 (35.7%, 95% CI 12.8-64.9) with ERBB2 expression below the median presented a confirmed objective response as compared to 3 of 10 (30%, 95% CI 6.7-65.2) with ERBB2 expression above the median. Although HER2 expression is a determinant of T-DXd efficacy, our study suggests that additional mechanisms may also be involved. (ClinicalTrials.gov identifier NCT04132960 .).
曲妥珠单抗-德鲁替康(T-DXd)是一种用于乳腺癌治疗的抗 HER2 药物偶联物,其作用机制和耐药机制仍不清楚。DAISY 二期试验评估了 T-DXd 用于 HER2 过表达(n=72,队列 1)、HER2 低表达(n=74,队列 2)和 HER2 无表达(n=40,队列 3)转移性乳腺癌患者的疗效。在全分析集人群(n=177)中,队列 1 的确认客观缓解率(主要终点)为 70.6%(95%置信区间(CI)58.3-81),队列 2 为 37.5%(95% CI 26.4-49.7),队列 3 为 29.7%(95% CI 15.9-47)。主要终点在队列 1 和 2 中达到。次要终点包括安全性。未观察到新的安全性信号。在治疗期间,HER2 表达肿瘤(n=4)呈现出强烈的 T-DXd 染色。相反,HER2 免疫组织化学 0 样本(n=3)呈现出无或极少 T-DXd 染色(皮尔逊相关系数 r=0.75,P=0.053)。在 HER2 免疫组织化学 0 转移性乳腺癌患者中,14 例中有 5 例(35.7%,95% CI 12.8-64.9)的 ERBB2 表达低于中位数,确认客观缓解率为 5 例(35.7%,95% CI 12.8-64.9),而 10 例中有 3 例(30%,95% CI 6.7-65.2)的 ERBB2 表达高于中位数。尽管 HER2 表达是 T-DXd 疗效的决定因素,但我们的研究表明,可能还涉及其他机制。(临床试验注册号 NCT04132960)。