首页> 美国卫生研究院文献>other >Chinese Herbal Medicine Combined With EGFR-TKI in EGFR Mutation-Positive Advanced Pulmonary Adenocarcinoma (CATLA): A Multicenter Randomized Double-Blind Placebo-Controlled Trial
【2h】

Chinese Herbal Medicine Combined With EGFR-TKI in EGFR Mutation-Positive Advanced Pulmonary Adenocarcinoma (CATLA): A Multicenter Randomized Double-Blind Placebo-Controlled Trial

机译:中草药联合EGFR-TKI治疗EGFR突变阳性晚期肺腺癌(CATLA):一项多中心随机双盲安慰剂对照试验

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background: To determine the clinical activity and safety of Chinese herbal medicine (CHM) combined with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI) in patients with advanced pulmonary adenocarcinoma (ADC) and the ability of CHM combined with EGFR-TKI to activate EGFR mutations. >Methods: Three hundred and fifty-four patients were randomly assigned to EGFR-TKI (erlotinib 150 mg/d, gefitinib 250 mg/d, or icotinib 125 mg tid/d) plus CHM (TKI+CHM, N = 185) or EGFR-TKI plus placebo (TKI+placebo, N = 169). Progression-free survival (PFS) was the primary end point; the secondary end points were overall survival (OS), objective response rate (ORR), disease control rate (DCR), quality of life [Functional Assessment of Cancer Therapy-Lung (FACT-L) and Lung Cancer Symptom Scale (LCSS)], and safety. >Results: The median PFS was significantly longer for the TKI+CHM group (13.50 months; 95% CI, 11.20–16.46 months) than with the EGFR-TKI group (10.94 months; 95% CI, 8.97–12.45 months; hazard ratio, 0.68; 95% CI, 0.51–0.90; P = 0.0064). The subgroup analyses favored TKI+CHM as a first-line treatment (15.97 vs. 10.97 months, P = 0.0447) rather than as a second-line treatment (11.43 vs. 9.23 months, P = 0.0530). Patients with exon 19 deletion had a significantly longer PFS than with 21 L858R. The addition of CHM to TKI significantly improved the ORR (64.32% vs. 52.66%, P = 0.026) and QoL. Drug-related grade 1–2 adverse events were less common with TKI+CHM. >Conclusions: TKI+CHM improved PFS when compared with TKI alone in patients with EGFR mutation-positive advanced non-small-cell lung cancer (NSCLC).Clinical Trial Registration: , identifier .
机译:>背景:确定中药(CHM)联合表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)在晚期肺腺癌(ADC)患者中的临床活性和安全性CHM与EGFR-TKI结合以激活EGFR突变。 >方法:将354例患者随机分配至EGFR-TKI(厄洛替尼150 mg / d,吉非替尼250 mg / d或艾克替尼125 mg tid / d)加CHM(TKI + CHM ,N = 185)或EGFR-TKI加安慰剂(TKI +安慰剂,N = 169)。无进展生存期(PFS)是主要终点。次要终点为总生存期(OS),客观缓解率(ORR),疾病控制率(DCR),生活质量[癌症治疗肺功能评估(FACT-L)和肺癌症状量表(LCSS)] , 和安全。 >结果:TKI + CHM组(13.50个月; 95%CI,11.20–16.46个月)的中位PFS明显长于EGFR-TKI组(10.94个月; 95%CI,8.97) –12.45个月;危险比:0.68; 95%CI,0.51-0.90; P = 0.0064)。该亚组分析了将TKI + CHM作为一线治疗(15.97比10.97个月,P = 0.0447),而不是作为二线治疗(11.43与9.23个月,P = 0.0530)。外显子19缺失的患者的PFS明显长于21 L858R。在TKI中添加CHM显着改善了ORR(64.32%比52.66%,P = 0.026)和QoL。与药物相关的1-2级不良事件在TKI + CHM中较少见。 >结论:与单纯TKI相比,EGFR突变阳性晚期非小细胞肺癌(NSCLC)患者的TKI + CHM改善了PFS。临床试验注册:,标识符。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号