Erlotinib for the treatment of brain metastases in non-small cell lung cancer

被引:29
|
作者
Brower, Jeffrey V. [1 ]
Robins, H. Ian [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Hosp & Clin, Carbone Canc Ctr, Dept Human Oncol, 600 Highland Ave,K4-534, Madison, WI 53792 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, 600 Highland Ave,K4-534, Madison, WI 53792 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Dept Neurol, 600 Highland Ave,K4-534, Madison, WI 53792 USA
关键词
Erlotinib; non-small cell lung cancer; brain metastases; radiotherapy; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; DOSE WEEKLY ERLOTINIB; EGFR MUTATION STATUS; PHASE-II TRIAL; RADIATION-THERAPY; STEREOTACTIC RADIOSURGERY; LEPTOMENINGEAL METASTASES; PERFORMANCE STATUS; GEFITINIB;
D O I
10.1517/14656566.2016.1165206
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Brain metastases (BM) are a common and lethal complication of non-small cell lung cancer (NSCLC) with up to 40% experiencing this complication. The use of erlotinib, a small molecule epidermal growth factor receptor (EGFR) inhibitor, holds promise in this somewhat refractory cohort of patients, and has become the subject of active clinical investigation. Areas covered: This review covers the preclinical and clinical studies of erlotonib as it relates to its use in the treatment of NSCLC patients with BM. A literature search in part utilized the PubMed database up through Dec 2015. Expert opinion: Preclinical and retrospective data for erlotinib provide evidence of CNS penetration, and objective responses in the setting of BM from EGFR mutated NSCLC. Phase I and II data have demonstrated the feasibility of concomitant delivery of erlotinib and WBRT in the treatment of BM from NSCLC. Phase II/III data however, from non-EGFR mutation enriched populations, have demonstrated no benefit in progression free or overall survival with the addition of erlotinib to metastasis directed radiotherapy. Currently the utilization of erlotinib with WBRT or SRS is therefore investigational and may be a reasonable option in erlotinib naive, EGFR mutated patients with refractory BM.
引用
收藏
页码:1013 / 1021
页数:9
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