Have adjuvant tyrosine kinase inhibitors lost their shine?

被引:1
|
作者
Sabari, Joshua K. [1 ]
Chaft, Jamie E. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Thorac Oncol Serv, 300 E 66th St, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY USA
关键词
Non-small cell lung cancer (NSCLC); epidermal growth factor receptor (EGFR); tyrosine kinase inhibitor (TKI); adjuvant; erlotinib; gefitinib; afatinib; CELL LUNG-CANCER; GEFITINIB; ERLOTINIB; MUTATION; CHEMOTHERAPY; PLACEBO; CHEMORADIOTHERAPY; MULTICENTER; DOCETAXEL; RECEPTOR;
D O I
10.21037/atm.2016.07.18
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite broad advances in molecularly targeted therapies, lung cancer remains the leading cause of cancer related mortality in the United States. Epidermal growth factor receptor (EGFR) mutations occur in approximately 17% of advanced non-small cell lung cancer (NSCLC) in the US population. The remarkable efficacy of small-molecule EGFR tyrosine kinase inhibitors (TKIs) in this unique subset of patients has revolutionized the therapeutic approach to lung cancer. The success of these agents in the metastatic setting leads to the logical question of what role these drugs may have in the adjuvant setting for patients with earlier stage disease. RADIANT, an international randomized, double-blind, placebo controlled phase III study in patients with completely resected stage IB to IIIA NSLC whose tumors expressed EGFR by IHC and EGFR amplification by FISH, attempted to answer the question of whether erlotinib would improve disease free survival and overall survival in the adjuvant setting. While RADIANT does not conclude for or against adjuvant use of EGFR-TKIs, all data points towards benefit in a selected population. As clinicians, we must continue to enroll to potentially practice changing therapeutic neoadjuvant and adjuvant chemotherapy studies internationally.
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页数:4
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