The Emerging Therapeutic Landscape of ALK Inhibitors in Non-Small Cell Lung Cancer

被引:51
|
作者
Gristina, Valerio [1 ]
La Mantia, Maria [1 ]
Iacono, Federica [1 ]
Galvano, Antonio [1 ]
Russo, Antonio [1 ]
Bazan, Viviana [2 ]
机构
[1] Univ Palermo, Dept Surg Oncol & Oral Sci, I-90127 Palermo, Italy
[2] Univ Palermo, Sect Med Oncol, Dept Biomed Neurosci & Adv Diagnost BiND, I-90127 Palermo, Italy
关键词
non-small cell lung cancer (NSCLC); tyrosine kinase inhibitors (TKIs); ALK inhibitors; crizotinib; ceritinib; alectinib; brigatinib; lorlatinib; ensartinib; ANAPLASTIC LYMPHOMA KINASE; OPEN-LABEL; ANTITUMOR-ACTIVITY; SINGLE-ARM; PD-L1; EXPRESSION; J-ALEX; CRIZOTINIB; CERITINIB; ALECTINIB; SAFETY;
D O I
10.3390/ph13120474
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The treatment of metastatic non-small cell lung cancer (NSCLC) has undergone a paradigm shift over the last decade. Better molecular characterization of the disease has led to the rapid improvement of personalized medicine and the prompt delivery of targeted therapies to patients with NSCLC. The discovery of the EML4-ALK fusion gene in a limited subset of patients affected by NSCLC and the subsequent clinical development of crizotinib in 2011 has been an impressive milestone in lung cancer research. Unfortunately, acquired resistances regularly develop, hence disease progression occurs. Afterward, modern tyrosine kinase inhibitors (TKIs), such as ceritinib, alectinib, brigatinib, and lorlatinib, have been approved by the Food and Drug Administration (FDA) for the management of anaplastic lymphoma kinase (ALK)-positive NSCLCs. Several compounds are currently under investigation to achieve the optimal strategy of therapy. Additionally, the results of ongoing clinical trials with novel-generation TKI will provide more evidence on the best sequence in the treatment of ALK-positive NSCLC patients. In this review, we provide a comprehensive overview of the state-of-the-art targeted therapy options in ALK-positive NSCLCs. Resistance, potential therapeutic strategies to overcome drug resistance, and future perspectives for this subset of patients are critically analyzed and summarized.
引用
收藏
页码:1 / 23
页数:23
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