Perez Jose, Garrigós Laia, Gion Maria, Jänne Pasi A, Shitara Kohei, Siena Salvatore, Cortés Javier
International Breast Cancer Center, Quiron Group, Barcelona, Spain.
Medical Department, Medica Scientia Innovation Research (MedSIR), Valencia, Spain.
Expert Opin Biol Ther. 2021 Jul;21(7):811-824. doi: 10.1080/14712598.2021.1890710. Epub 2021 Apr 1.
Despite the substantial improvements made in human epidermal growth factor receptor 2 (HER2)-targeted therapies since the approval of trastuzumab more than 20 years ago, there is still considerable unmet need in patients with HER2-expressing breast cancer (BC) and other solid tumors. Trastuzumab deruxtecan (T-DXd) is a newer antibody-drug conjugate approved for the treatment of metastatic breast cancer (BC) and gastric cancer (GC) and is under active investigation in other solid tumors, including non-small cell lung cancer, colorectal cancer, and HER2-low tumors.
The current treatment and investigational landscape of HER2-positive and HER2-low metastatic BC (mBC) and the preclinical and clinical trials investigating T-DXd. To identify relevant literature, a search was performed on English-language publications and congress abstracts.
T-DXd is likely to become the standard of care for second-line treatment of HER2-positive mBC, and it may play a role in the treatment of hormone receptor-positive and triple-negative mBC with HER2-low expression. Because it was recently approved in the United States and Japan to treat HER2-positive metastatic GC, it holds promise for the treatment of other HER2-positive solid tumors, including colorectal cancer, non-small cell lung cancer, and HER2-low BC.
尽管自20多年前曲妥珠单抗获批以来,针对人表皮生长因子受体2(HER2)的疗法有了显著改进,但HER2表达型乳腺癌(BC)和其他实体瘤患者仍有相当大的未满足需求。曲妥珠单抗德曲妥珠单抗(T-DXd)是一种较新的抗体药物偶联物,已获批用于治疗转移性乳腺癌(BC)和胃癌(GC),目前正在其他实体瘤中进行积极研究,包括非小细胞肺癌、结直肠癌和HER2低表达肿瘤。
HER2阳性和HER2低表达转移性乳腺癌(mBC)的当前治疗和研究现状,以及研究T-DXd的临床前和临床试验。为了识别相关文献,对英文出版物和会议摘要进行了检索。
T-DXd可能会成为HER2阳性mBC二线治疗的标准疗法,并且可能在治疗激素受体阳性和HER2低表达的三阴性mBC中发挥作用。由于它最近在美国和日本获批用于治疗HER2阳性转移性GC,因此有望用于治疗其他HER2阳性实体瘤,包括结直肠癌、非小细胞肺癌和HER2低表达BC。