Zhang Yalei, Yang Haihong, Yang Xinyun, Deng Qiuhua, Zhao Meilin, Xu Xin, He Jianxing
Department of Cardiothoracic Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510120, P.R. China ; State Key Laboratory of Respiratory Diseases, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510120, P.R. China.
State Key Laboratory of Respiratory Diseases, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510120, P.R. China ; Department of Pharmacy, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510120, P.R. China ;
Mol Clin Oncol. 2014 May;2(3):449-453. doi: 10.3892/mco.2014.256. Epub 2014 Feb 11.
Erlotinib and pemetrexed have been approved for the second-line treatment of non-small cell lung cancer. Recent reports indicated that erlotinib and pemetrexed exerted synergistic effects against lung adenocarcinoma. The available treatment options for lung cancer with brain metastases (BM) are currently limited. In the present study, we investigated the efficacy of the combined administration of erlotinib and pemetrexed in 9 patients with epidermal growth factor receptor () wild-type lung adenocarcinoma with BM. Pemetrexed (500 mg/m) and cisplatin (20 mg/m) were administered on day 1 and days 1-3, respectively. Erlotinib (150 mg) was administered daily on days 4-20. The 9 patients harbored wild-type mutation in the primary tumor tissues. With regard to the BM, no patients achieved complete remission, 7 patients exhibited a partial response (PR), 1 had stable disease (SD) and 1 had progressive disease (PD). As regards the extracranial tumors, 3 patients exhibited a PR, 2 had SD, 3 had PD and 1 was not applicable. The performance status and the symptoms improved in 3 patients following treatment. The median progression-free survival for intracranial and extracranial disease control was 179 and 146.5 days, respectively. The median overall survival was 197.4 days. Therefore, erlotinib combined with pemetrexed/cisplatin, was found to be effective in the treatment of patients with wild-type lung adenocarcinoma.
厄洛替尼和培美曲塞已被批准用于非小细胞肺癌的二线治疗。最近的报告表明,厄洛替尼和培美曲塞对肺腺癌具有协同作用。目前,肺癌脑转移(BM)的可用治疗选择有限。在本研究中,我们调查了厄洛替尼和培美曲塞联合给药对9例表皮生长因子受体()野生型肺腺癌伴BM患者的疗效。培美曲塞(500 mg/m)和顺铂(20 mg/m)分别在第1天和第1 - 3天给药。厄洛替尼(150 mg)在第4 - 20天每日给药。这9例患者的原发肿瘤组织存在野生型突变。关于BM,没有患者达到完全缓解,7例患者表现出部分缓解(PR),1例病情稳定(SD),1例病情进展(PD)。关于颅外肿瘤,3例患者表现出PR,2例SD,3例PD,1例不适用。3例患者治疗后体能状态和症状有所改善。颅内和颅外疾病控制的无进展生存期中位数分别为179天和146.5天。总生存期中位数为197.4天。因此,发现厄洛替尼联合培美曲塞/顺铂对野生型肺腺癌患者的治疗有效。