Medical Oncology Department, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Medical Oncology Department, Tianjin Haihe Hospital, Tianjin, China.
Thorac Cancer. 2018 Jun;9(6):693-698. doi: 10.1111/1759-7714.12632. Epub 2018 Apr 14.
EGFR-tyrosine kinase inhibitors (TKIs) combined with TS-1 might overcome EGFR-TKI resistance, which has been indicated by several preclinical studies. We investigated the synergistic efficacy and safety of the combination therapy of EGFR-TKIs and TS-1 in non-small cell lung cancer (NSCLC) patients with acquired resistance to previous EGFR-TKI therapy.
This was a phase II, single-arm and single-center prospective study. Stage IIIB-IV NSCLC patients with acquired resistance to prior EGFR-TKI treatment were enrolled. All patients were administered combination therapy of TS-1 and continuing EGFR-TKIs in this study. The primary endpoints were progression-free survival (PFS), while overall survival (OS), disease control rate (DCR), and safety were secondary endpoints.
A total of 42 patients with acquired resistance to EGFR-TKIs were eligible for this study. The median PFS for all patients was five months (95% confidence interval [CI] 3.6-5.4). The OS and DCR were 31.9 (95% CI 17.8-46.0) months and 69.0% (29/42), respectively. No grade 4 toxicity or grade 3 hematologic toxicity was observed in this study. One patient (2%) experienced grade 3 elevated total serum bilirubin.
The combination treatment of TS-1 and EGFR-TKIs was effective and well tolerated by patients who had experienced prior EGFR-TKI treatment failure. Our results need to be validated by larger prospective clinical trials.
几项临床前研究表明,表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)联合替吉奥(TS-1)可能克服 EGFR-TKI 耐药。我们研究了 EGFR-TKI 和 TS-1 联合治疗对先前 EGFR-TKI 治疗耐药的非小细胞肺癌(NSCLC)患者的协同疗效和安全性。
这是一项 II 期、单臂、单中心前瞻性研究。招募了先前 EGFR-TKI 治疗耐药的 IIIB-IV 期 NSCLC 患者。所有患者在这项研究中均接受 TS-1 和持续 EGFR-TKIs 的联合治疗。主要终点是无进展生存期(PFS),次要终点包括总生存期(OS)、疾病控制率(DCR)和安全性。
共有 42 名 EGFR-TKI 耐药的患者符合本研究条件。所有患者的中位 PFS 为 5 个月(95%置信区间[CI] 3.6-5.4)。OS 和 DCR 分别为 31.9 个月(95%CI 17.8-46.0)和 69.0%(29/42)。本研究未观察到 4 级毒性或 3 级血液学毒性。1 名患者(2%)出现 3 级总胆红素升高。
TS-1 和 EGFR-TKIs 的联合治疗对先前 EGFR-TKI 治疗失败的患者是有效且耐受良好的。我们的结果需要通过更大的前瞻性临床试验来验证。