Gouda Mohamed A, Gonugunta Amrit, Dumbrava Ecaterina E, Yap Timothy A, Rodon Jordi, Piha-Paul Sarina A, Pohlmann Paula R, Damodaran Senthil, Murthy Rashmi, Valero Vicente, Mouabbi Jason A, Tripathy Debasish, Sahin Aysegul A, Chen Hui, Meric-Bernstam Funda
Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas.
Clin Cancer Res. 2025 Apr 1;31(7):1268-1274. doi: 10.1158/1078-0432.CCR-24-3468.
Trastuzumab deruxtecan (T-DXd) is currently approved for treating metastatic breast cancer (MBC) that is HER2 positive [immunohistochemistry (IHC) score of 3+ or in situ hybridization (ISH) positivity] or HER2-low (IHC score of 1+ or IHC 2+/ISH negative), as well as for HER2-positive gastric cancer, HER2-mutant lung cancer, and HER2-overexpressing solid tumors. Given the increasing utilization of T-DXd, we sought to determine how HER2 status might change following T-DXd therapy.
We retrospectively reviewed patients with MBC who received T-DXd at the University of Texas MD Anderson Cancer Center. We included patients with paired pre- and post-treatment biopsies assessed for HER2 status using IHC.
We included 41 patients with MBC who received treatment with T-DXd and had paired pre- and post-treatment biopsies assessed for HER2 status using IHC. HER2 loss was observed in 11 patients [32.4% of 34 patients with pre-treatment HER2 expression (1+, 2+, or 3+)] following treatment with T-DXd. In addition to the 11 patients with HER2 loss, another 10 patients (29.4%) had a decrease in HER2 score after treatment with T-DXd.
HER2 loss and decrease in HER2 expression are common in patients with MBC receiving treatment with T-DXd. Reevaluation of HER2 status following T-DXd treatment should be considered prior to alternate HER2-targeted therapies that require HER2 overexpression for efficacy.
曲妥珠单抗德鲁昔单抗(T-DXd)目前已被批准用于治疗人表皮生长因子受体2(HER2)阳性的转移性乳腺癌(MBC)[免疫组织化学(IHC)评分为3+或原位杂交(ISH)阳性]或HER2低表达(IHC评分为1+或IHC 2+/ISH阴性),以及HER2阳性胃癌、HER2突变型肺癌和HER2过表达实体瘤。鉴于T-DXd的使用越来越多,我们试图确定T-DXd治疗后HER2状态可能如何变化。
我们回顾性分析了在德克萨斯大学MD安德森癌症中心接受T-DXd治疗的MBC患者。我们纳入了使用IHC评估HER2状态的配对治疗前和治疗后活检的患者。
我们纳入了41例接受T-DXd治疗且使用IHC评估了配对治疗前和治疗后活检的HER2状态的MBC患者。在用T-DXd治疗后,在11例患者中观察到HER2缺失[34例治疗前HER2表达为(1+、2+或3+)的患者中的32.4%]。除了11例HER2缺失的患者外,另外10例患者(29.4%)在接受T-DXd治疗后HER2评分降低。
HER2缺失和HER2表达降低在接受T-DXd治疗的MBC患者中很常见。在需要HER2过表达才能起效的替代HER2靶向治疗之前,应考虑在T-DXd治疗后重新评估HER2状态。