Department of Respiratory and Critical Care Medicine, The People's Hospital of Kaizhou District, China.
Department of Respiratory and Critical Care Medicine, The People's Hospital of Bishan District, China.
Clinics (Sao Paulo). 2023 Jan 19;78:100152. doi: 10.1016/j.clinsp.2022.100152. eCollection 2023.
This study aimed to perform a meta‑analysis comparing the efficacy and safety of gefitinib in combination with chemotherapy versus gefitinib alone in patients with advanced Non‑Small Cell Lung Cancer (NSCLC). We searched databases for clinical studies that reported the efficacy or safety of gefitinib plus chemotherapy in comparison with gefitinib alone. Raw data from included studies were extracted and pooled to calculate the Odds Ratio (OR) for Objective Response Rate (ORR) and Disease Control Rate (DCR), the Hazard Ratio (HR) for Progression-Free Survival (PFS) and Overall Survival (OS), and OR for complication ≥ Grade 3. A total of 10 studies containing 1,528 patients with NSCLC were identified and included in the analysis. Gefitinib plus chemotherapy showed significantly better efficacy in improving ORR (OR = 1.54; 95% CI [Confidence Interval], 1.13‒2.1; p = 0.006), DCR (OR = 1.62; 95% CI 1.14‒2.29; p = 0.007), PFS (HR=1.67; 95% CI 1.45‒1.94; p < 0.001) and OS (HR = 1.49; 95% CI 1.2‒1.87; p < 0.001) as compared with gefitinib alone. Consistent results were observed in the sub-population with positive EGFR mutation. The combination of gefitinib with chemotherapy had a significantly higher risk of complication (≥ Grade 3) with an OR of 3.29 (95% CI 2.57‒4.21; p < 0.001). The findings in the present study suggest that the combination of gefitinib with chemotherapy can provide better disease response and survival outcomes for patients with advanced NSCLC.
本研究旨在进行一项荟萃分析,比较吉非替尼联合化疗与吉非替尼单药治疗晚期非小细胞肺癌(NSCLC)的疗效和安全性。我们检索了数据库中报道吉非替尼联合化疗与吉非替尼单药比较疗效或安全性的临床研究。从纳入的研究中提取原始数据并进行合并,以计算客观缓解率(ORR)和疾病控制率(DCR)的优势比(OR)、无进展生存期(PFS)和总生存期(OS)的风险比(HR),以及≥3 级并发症的 OR。共纳入 10 项包含 1528 例 NSCLC 患者的研究进行分析。吉非替尼联合化疗在提高 ORR(OR=1.54;95%CI[置信区间],1.13‒2.1;p=0.006)、DCR(OR=1.62;95%CI 1.14‒2.29;p=0.007)、PFS(HR=1.67;95%CI 1.45‒1.94;p<0.001)和 OS(HR=1.49;95%CI 1.2‒1.87;p<0.001)方面均优于吉非替尼单药。在 EGFR 阳性突变的亚组中观察到了一致的结果。吉非替尼联合化疗的并发症(≥3 级)风险显著增加,OR 为 3.29(95%CI 2.57‒4.21;p<0.001)。本研究的结果表明,吉非替尼联合化疗可为晚期 NSCLC 患者提供更好的疾病缓解和生存结局。