Emerging treatment using tubulin inhibitors in advanced non-small cell lung cancer

被引:45
作者
Hardin, C. [1 ]
Shum, E. [1 ]
Singh, A. P. [1 ]
Perez-Soler, R. [1 ]
Cheng, H. [1 ]
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med Oncol, 111 E 210th St, Bronx, NY 10467 USA
关键词
Adenocarcinoma; docetaxel; microtubule; tubulin; tubulin inhibitor; novel; NSCLC; paclitaxel; squamous cell; vinorelbine; PHASE-III TRIAL; PACLITAXEL PLUS CARBOPLATIN; PLATINUM-BASED CHEMOTHERAPY; ADVANCED SOLID TUMORS; ONCOLOGY-GROUP TRIAL; FRONT-LINE TREATMENT; RANDOMIZED CONTROLLED-TRIAL; ERIBULIN MESYLATE E7389; EVERY; WEEKS; BETA-TUBULIN;
D O I
10.1080/14656566.2017.1316374
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Tubulin inhibitors including taxanes and vinca alkaloids are important components of chemotherapy regimens used in advanced non-small cell lung cancer (NSCLC). Despite a treatment paradigm shift due to molecularly-targeted therapies and immunotherapy, a majority of patients will receive chemotherapy during their treatment course. Either used alone or in combination, tubulin inhibitors have demonstrated clinical benefits in different settings of lung cancer management.Areas covered: This review first discusses FDA-approved tubulin inhibitors for NSCLC, such as paclitaxel, docetaxel, vinorelbine, and nab-paclitaxel. The article then provides a summary of novel tubulin inhibitors, including cabazitaxel, eribulin, ixabepilone, patupilone, plinabulin, new colchicine analogues and others. It also discusses new tubulin inhibitor combinations with immunotherapy (PD-1/PD-L1 inhibitors) and molecularly-targeted therapies (e.g. anti-angiogenic agents, mTOR inhibitors, heat shock protein 90 inhibitors, MEK inhibitors, and anti-HER3 agents). Lastly, emerging data on potential resistance mechanisms and predictive biomarkers for tubulin inhibitors are explored.Expert opinion: Tubulin inhibitors will likely continue to play important roles in NSCLC management due to the advent of novel agents and combinations. Through further understanding of tumor biology, investigation of drug resistance, and development of predictive biomarkers, we will be better positioned to incorporate microtubule inhibition into patient specific treatment strategies.
引用
收藏
页码:701 / 716
页数:16
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