肺癌
医学
免疫疗法
癌症治疗
癌症
嵌合抗原受体
癌症研究
后天抵抗
抗药性
酪氨酸激酶
肿瘤科
内科学
生物
受体
微生物学
作者
May-Lucie Meyer,Bailey G Fitzgerald,Luis Paz‐Ares,Federico Cappuzzo,Pasi A. Jänne,Solange Peters,Fred R. Hirsch
出处
期刊:The Lancet
[Elsevier]
日期:2024-08-01
卷期号:404 (10454): 803-822
被引量:2
标识
DOI:10.1016/s0140-6736(24)01029-8
摘要
Targeted therapies and immunotherapies have radically improved treatment for advanced non-small-cell lung cancer (NSCLC). Tyrosine kinase inhibitors targeting oncogenic driver mutations continue to evolve over multiple generations to enhance effectiveness and tackle drug resistance. Immune checkpoint inhibitors remain integral for the treatment of NSCLCs that do not have specific actionable genetic mutations. Antibody-drug conjugates and bispecific antibodies are being integrated into treatment guidelines, and emerging therapies include T-cell engagers, cellular therapies, cancer vaccines, and external devices. Despite these advances, challenges remain in identifying predictive biomarkers to individually tailor treatments, abrogate resistance, reduce costs, and ensure optimal cancer treatment accessibility.
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