曲妥珠单抗
拉帕蒂尼
医学
帕妥珠单抗
卡培他滨
肿瘤科
曲妥珠单抗
紫杉烷
内科学
转移性乳腺癌
来那替尼
乳腺癌
艾瑞布林
癌症
结直肠癌
作者
Ruby Gupta,Sachin Gupta,Bana Antonios,Bipin Ghimire,Vishal Jindal,Jaskiran Deol,Suzanna Gaikazian,Marianne Huben,Joseph Anderson,Michael Stender,Ishmael Jaiyesimi
标识
DOI:10.1007/s12032-022-01849-y
摘要
HER2-positive breast cancer is an aggressive subtype of breast cancer with five-year survival rates of 30% for the advanced stage. The development of anti-HER2 treatments has led to a paradigm shift in the management and clinical outcomes of advanced HER2-positive breast cancer patients. The standard first-line treatment consists of taxane-based chemotherapy plus dual anti-HER2 therapies with trastuzumab and pertuzumab. The antibody–drug conjugate (ADC) ado-trastuzumab emtansine (T-DM1) has been a second-line therapeutic standard, but the second-line treatment approach is rapidly evolving. Given a substantial advantage of another ADC, Fam-trastuzumab deruxtecan (T-DXd), compared to T-DM1 in a recent randomized trial in the second-line setting, T-DXd is currently the preferred second-line option. Optimal third-line treatment strategies are still not established, and multiple approaches have been used including combinations based on capecitabine, trastuzumab, or both with oral anti-HER2 tyrosine kinase inhibitors. Tucatinib plus capecitabine and trastuzumab, lapatinib plus trastuzumab, neratinib or lapatinib plus capecitabine are some of the FDA approved combinations. Another newer agent approved for third- or later-line therapy in the metastatic setting is margetuximab, an Fc-engineered anti-HER2 monoclonal antibody, in combination with chemotherapy. Other novel agents currently under clinical trials are the drugs that indirectly target HER2, including immune cell cycle inhibitors, PI3K/mTOR inhibitors, and immunotherapy agents.
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