Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Department of Medical Oncology, Hospital Clinic of Barcelona, Spain.
JCO Oncol Pract. 2021 Oct;17(10):594-604. doi: 10.1200/OP.21.00172. Epub 2021 Jun 2.
Human epidermal growth factor receptor 2 (HER2) is overexpressed and/or amplified in approximately 20% of breast cancers, conferring an aggressive tumor behavior but also an opportunity for targeted therapies. In the advanced setting, the prognosis of patients suffering from this disease has greatly improved after the introduction of new anti-HER2 drugs beyond trastuzumab. For most patients, a taxane combined with trastuzumab and pertuzumab in the first-line setting, followed by trastuzumab-emtansine in second line, should be considered the standard of care today. However, chemo-free anti-HER2 strategies in hormone receptor-positive, HER2-positive breast cancer could also be considered in selected patients. In the third-line setting and beyond, several emerging anti-HER2 therapies are becoming available, including tucatinib, fam-trastuzumab deruxtecan-nxki (DS-8201a), neratinib, and margetuximab-cmkb. In addition, new compounds and combinations are showing promising results in the late-line setting. The treatment landscape of HER2-positive advanced disease is evolving constantly, active drugs such as pertuzumab and trastuzumab-emtansine are moving to early-stage, many biomarkers, including quantification of HER2 itself, are being explored to improve patient selection, and patient populations with specific needs are emerging, such as those with brain metastasis. Here, we provide an overview of the current and future management of HER2-positive advanced breast cancer.
人类表皮生长因子受体 2(HER2)在大约 20%的乳腺癌中过度表达和/或扩增,赋予肿瘤侵袭性,但也为靶向治疗提供了机会。在晚期,HER2 阳性乳腺癌患者在曲妥珠单抗以外的新型抗 HER2 药物问世后,预后得到了极大改善。对于大多数患者,紫杉烷联合曲妥珠单抗和帕妥珠单抗作为一线治疗,然后二线使用曲妥珠单抗-美坦新偶联物(T-DM1),应被视为目前的标准治疗。然而,在选择的患者中,也可以考虑激素受体阳性、HER2 阳性乳腺癌的无化疗抗 HER2 策略。在三线及以上治疗中,几种新的抗 HER2 治疗方法正在出现,包括图卡替尼、fam-trastuzumab deruxtecan-nxki(DS-8201a)、奈拉替尼和马吉妥昔单抗-cmkb。此外,新的化合物和组合在晚期治疗中显示出有希望的结果。HER2 阳性晚期疾病的治疗格局正在不断发展,曲妥珠单抗和 T-DM1 等活性药物正在向早期转移,许多生物标志物,包括 HER2 本身的定量,正在被探索以改善患者选择,具有特定需求的患者群体正在出现,如脑转移患者。在这里,我们概述了 HER2 阳性晚期乳腺癌的当前和未来的管理。