Okines Alicia F C, Curigliano Giuseppe, Mizuno Nobumasa, Oh Do-Youn, Rorive Andree, Soliman Hatem, Takahashi Shunji, Bekaii-Saab Tanios, Burkard Mark E, Chung Ki Y, Debruyne Philip R, Fox Jenny R, Gambardella Valentina, Gil-Martin Marta, Hamilton Erika P, Monk Bradley J, Nakamura Yoshiaki, Nguyen Danny, O'Malley David M, Olawaiye Alexander B, Pothuri Bhavana, Reck Martin, Sudo Kazuki, Sunakawa Yu, Van Marcke Cedric, Yu Evan Y, Ramos Jorge, Tan Sherry, Bieda Mark, Stinchcombe Thomas E, Pohlmann Paula R
The Royal Marsden NHS Foundation Trust, London, UK.
Istituto Europeo di Oncologia, IRCCS, Milan, Italy.
Nat Med. 2025 Mar;31(3):909-916. doi: 10.1038/s41591-024-03462-0. Epub 2025 Jan 17.
Human epidermal growth factor receptor 2 (HER2, also known as ERBB2) signaling promotes cell growth and differentiation, and is overexpressed in several tumor types, including breast, gastric and colorectal cancer. HER2-targeted therapies have shown clinical activity against these tumor types, resulting in regulatory approvals. However, the efficacy of HER2 therapies in tumors with HER2 mutations has not been widely investigated. SGNTUC-019 is an open-label, phase 2 basket study evaluating tucatinib, a HER2-targeted tyrosine kinase inhibitor, in combination with trastuzumab in patients with HER2-altered solid tumors. The study included a cohort of 31 heavily pretreated female patients with HER2-mutated metastatic breast cancer who were also HER2 negative per local testing. Hormone receptor (HR)-positive patients also received fulvestrant. The overall response rate (primary endpoint) was 41.9% (90% confidence interval (CI): 26.9-58.2). Secondary endpoints of duration of response and progression-free survival were 12.6 months (90% CI: 4.7 to not estimable) and 9.5 months (90% CI: 5.4-13.8), respectively. No new safety signals were detected. Responses were observed across various HER2 mutations, including mutations in the tyrosine kinase and extracellular domains. The chemotherapy-free regimen of tucatinib and trastuzumab showed clinically meaningful antitumor activity with durable responses and favorable tolerability in heavily pretreated patients with HER2 mutations. These data support further investigation of HER2-targeted therapies in this patient population. ClinicalTrials.gov registration: NCT04579380 .
人表皮生长因子受体2(HER2,也称为ERBB2)信号传导促进细胞生长和分化,在包括乳腺癌、胃癌和结直肠癌在内的几种肿瘤类型中过表达。HER2靶向疗法已显示出针对这些肿瘤类型的临床活性,并获得了监管部门的批准。然而,HER2疗法在具有HER2突变的肿瘤中的疗效尚未得到广泛研究。SGNTUC-019是一项开放标签的2期篮子研究,评估HER2靶向酪氨酸激酶抑制剂图卡替尼与曲妥珠单抗联合用于HER2改变的实体瘤患者。该研究纳入了31名经过大量预处理的HER2突变转移性乳腺癌女性患者队列,根据当地检测,这些患者HER2也呈阴性。激素受体(HR)阳性的患者还接受了氟维司群治疗。总缓解率(主要终点)为41.9%(90%置信区间(CI):26.9-58.2)。缓解持续时间和无进展生存期的次要终点分别为12.6个月(90%CI:4.7至不可估计)和9.5个月(90%CI:5.4-13.8)。未检测到新的安全信号。在各种HER2突变中均观察到缓解,包括酪氨酸激酶和细胞外结构域的突变。图卡替尼和曲妥珠单抗的无化疗方案在经过大量预处理的HER2突变患者中显示出具有临床意义的抗肿瘤活性,缓解持久且耐受性良好。这些数据支持在该患者群体中进一步研究HER2靶向疗法。ClinicalTrials.gov注册号:NCT04579380 。