Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors for Non-Small-Cell Lung Cancer Patients with Leptomeningeal Carcinomatosis

被引:134
|
作者
Liao, Bin-Chi [1 ]
Lee, Jih-Hsiang [1 ,2 ]
Lin, Chia-Chi [1 ,3 ]
Chen, Ya-Fang [4 ]
Chang, Chin-Hao [2 ]
Ho, Chao-Chi [5 ]
Shih, Jin-Yuan [5 ]
Yu, Chong-Jen [5 ]
Yang, James Chih-Hsin [1 ,6 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Med Res, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Urol, Taipei 10764, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Med Imaging, Taipei 100, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[6] Natl Taiwan Univ, Coll Med, Grad Inst Oncol, Taipei 10764, Taiwan
关键词
Epidermal growth factor receptor tyrosine kinase inhibitor; Leptomeningeal carcinomatosis; Non-small-cell lung cancer; Prognosis; Whole-brain radiation therapy; DOSE WEEKLY ERLOTINIB; EGFR MUTATION; 1ST-LINE GEFITINIB; ACQUIRED-RESISTANCE; DISEASE RECURRENCE; BRAIN METASTASES; GOOD RESPONSE; OPEN-LABEL; CHEMOTHERAPY; ADENOCARCINOMA;
D O I
10.1097/JTO.0000000000000669
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Leptomeningeal carcinomatosis (LC) is a detrimental complication of patients with non-small-cell lung cancer (NSCLC). The effect of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) on the clinical outcome of these patients, particularly those with EGFR mutations, has not been studied yet. Methods: We searched the database for lung cancer patients diagnosed from 2003 to 2010 in one Asian medical center. NSCLC patients who also had LC diagnosed by either cytology or brain neuroimaging studies were identified. The treatments and clinical outcomes were reviewed. Results: Of 5526 lung cancer patients, we identified 212 (3.8%) NSCLC patients with LC. Most patients (88.7%) had adenocarcinoma histology, and 129 (60.9%) patients had been treated with at least one regimen of EGFR TKI before the diagnosis of LC. One hundred and twenty-four (58.5%) patients were treated with EGFR TKI, and 128 (60.4%) patients were treated with whole-brain radiation therapy (WBRT) after the diagnosis of LC. The median overall survival was 4.5 months (95% confidence interval, 3.5-7.3). Multivariate analysis suggested that EGFR TKI therapy, WBRT, and cytotoxic chemotherapy were independent predictors for longer survival. Mutational status of EGFR was evaluated in 101 patients, and 75 mutations (74.3%) were detected. Among the 75 patients with EGFR mutations, EGFR TKI therapy and cytotoxic chemotherapy after diagnosis of LC remained the independent factors predictive of extended survival in the multivariate analysis. Conclusions: Treatment of LC with EGFR TKI, cytotoxic chemotherapy, or WBRT in selected patients is associated with prolong survival period. These treatment options, especially EGFR TKIs, should be studied in patients with EGFR mutation-positive NSCLC and LC.
引用
收藏
页码:1754 / 1761
页数:8
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