Jin Yi-Hua, Li Wei-Hong, Bai Yan, Ni Lei
Department of Emergency.
Department of Hematology, First Affiliated Hospital of Jiamusi University, Jiamusi, China.
Medicine (Baltimore). 2019 Mar;98(10):e14785. doi: 10.1097/MD.0000000000014785.
This study evaluated the efficacy and toxicity of erlotinib and celecoxib (EC) for treating Chinese patients with advanced non-small cell lung cancer (ANSCLC) and epidermal growth factor receptor (EGFR) wild type.Totally, 75 subjects with ANSCLC and EGFR wild type were included. They all underwent EC treatment. The outcome measurements consisted of progression-free survival (PFS), overall survival (OS), complete response (CR), partial response (PR), stable disease (SD), progress disease (PD), and disease control rate (DCR). Additionally, adverse events were also documented.Two-year CR, PR, SD, PD, and DCR were 4.0%, 6.7%, 42.6%, 46.7%, and 53.3% respectively. The median PFS was 3.4 months, the median OS was 10.0 months. Additionally, acceptable toxicities were recorded in this study.The results showed that EC may be efficacious for patients with ANSCLC and EGFR wild type only, and acceptable toxicity among the Chinese Han population.
本研究评估了厄洛替尼与塞来昔布(EC)联合治疗中国晚期非小细胞肺癌(ANSCLC)且表皮生长因子受体(EGFR)野生型患者的疗效和毒性。总共纳入了75例ANSCLC且EGFR野生型的受试者。他们均接受了EC治疗。观察指标包括无进展生存期(PFS)、总生存期(OS)、完全缓解(CR)、部分缓解(PR)、疾病稳定(SD)、疾病进展(PD)和疾病控制率(DCR)。此外,还记录了不良事件。两年的CR、PR、SD、PD和DCR分别为4.0%、6.7%、42.6%、46.7%和53.3%。中位PFS为3.4个月,中位OS为10.0个月。此外,本研究记录了可接受的毒性。结果表明,EC可能仅对ANSCLC且EGFR野生型患者有效,且在中国汉族人群中具有可接受的毒性。