Yao Jialin, Lu Yan, Jiao Lijing, Bi Ling, Yang Wenxiao, Su Lingzi, Shi Jun, Wang Zhe, Gong Yabin, Xu Ling
Department of Oncology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Institute of Clinical Immunology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2022 Apr 1;13:840889. doi: 10.3389/fphar.2022.840889. eCollection 2022.
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (EGFR-TKIs) significantly improve the prognosis of non-small cell lung cancer (NSCLC) with EGFR mutation-positive. Although third-generation EGFR-TKI osimertinib is demonstrated with superior efficacy compared with first-generation EGFR-TKIs, acquired resistance to EGFR-TKIs remains the bottleneck. The Chinese herbal medicine (CHM) Yiqi-Yangyin-Jiedu decoction (YYJD) has been shown to delay acquired resistance to first-generation EGFR-TKIs in the CATLA study, but there is no high-level evidence for its effect when combined with osimertinib. This trial aims to evaluate the efficacy and safety of YYJD combined with osimertinib as first-line treatment in EGFR mutation-positive advanced NSCLC. This is a double-blind, multi-center, randomized controlled trial conducted in eight hospitals in China. A total of 314 participants will be randomly assigned to the osimertinib plus YYJD group (O+YYJD) or the osimertinib plus placebo group (O+placebo). Treatment will last until disease progression or death. Patients diagnosed with advanced NSCLC harboring EGFR Ex19del or L858R will be enrolled if they are ready to take osimertinib as first-line treatment, aged 18-74 years old, and provide signed informed consent. The primary outcome is progression-free survival (PFS). The secondary outcomes include a comparison of overall survival (OS), objective response rate (ORR), disease control rate (DCR), and quality of life (QoL). The analysis will be based on intention-to-treat and per-protocol subject analysis principles. The goal of this trial is to evaluate the efficacy and safety of YYJD when added to osimertinib as first-line treatment in EGFR mutation-positive advanced NSCLC.
表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(EGFR-TKIs)可显著改善表皮生长因子受体突变阳性的非小细胞肺癌(NSCLC)患者的预后。尽管第三代EGFR-TKI奥希替尼已被证明与第一代EGFR-TKIs相比具有更高的疗效,但对EGFR-TKIs产生获得性耐药仍然是一个瓶颈。在CATLA研究中,中药益气养阴解毒汤(YYJD)已被证明可延缓对第一代EGFR-TKIs的获得性耐药,但尚无其与奥希替尼联合使用效果的高级别证据。本试验旨在评估YYJD联合奥希替尼作为EGFR突变阳性晚期NSCLC一线治疗的疗效和安全性。这是一项在中国八家医院进行的双盲、多中心、随机对照试验。总共314名参与者将被随机分配到奥希替尼加YYJD组(O+YYJD)或奥希替尼加安慰剂组(O+安慰剂)。治疗将持续到疾病进展或死亡。如果被诊断为携带EGFR Ex19del或L858R的晚期NSCLC患者准备将奥希替尼作为一线治疗,年龄在18至74岁之间,并提供签署的知情同意书,则可入组。主要结局是无进展生存期(PFS)。次要结局包括总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)和生活质量(QoL)的比较。分析将基于意向性分析和符合方案受试者分析原则。本试验的目的是评估YYJD作为一线治疗添加到奥希替尼中用于EGFR突变阳性晚期NSCLC的疗效和安全性。