London Regional Cancer Program, Department of Oncology, Division of Medical Oncology.
Institute of Health Policy, Management and Evaluation, University of Toronto.
Am J Clin Oncol. 2019 May;42(5):440-445. doi: 10.1097/COC.0000000000000533.
The role of adjuvant tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC) is not well defined. Recent randomized controlled trials showed a disease-free survival (DFS) benefit in patients harboring an epidermal growth factor receptor (EGFR) mutation. Yet, older trials on patients with any EGFR status did not demonstrate the same benefit. We aimed to assess the efficacy and safety of adjuvant TKIs in NSCLC patients. The electronic databases Medline (PubMed) and EMBASE were searched for relevant randomized controlled trials. Random effect models were used. The primary outcome was DFS measured as hazard ratio (HR). The secondary outcomes were overall survival (OS) measured as HR, 2-year DFS and toxicity expressed as risk ratio and odds ratio (OR), respectively. Subgroup analyses assessed DFS by trial design. Six trials incorporating 1860 patients were included. In patients harboring an EGFR mutation, adjuvant TKIs decreased the risk of disease recurrence by 48% (HR: 0.52, 95% confidence interval [CI]: 0.35-0.78), improved 2-year DFS (HR: 0.53, 95% CI: 0.43-0.66) but did not improve OS (HR: 0.64, 95% CI: 0.22-1.89). The risk of developing ≥grade 3 skin toxicity (OR: 6.07, 95% CI: 4.34-8.51) and diarrhea (OR: 4.05; 95% CI: 2.44-6.74) was increased. In subgroup analyses, the DFS benefit was more pronounced in trials using TKIs over chemotherapy compared with trials using TKIs postchemotherapy. In conclusion, adjuvant TKIs decrease the risk of recurrence in NSCLC patients harboring an EGFR mutation but do not improve OS. Longer follow-up is needed for a definitive assessment of OS and to define the role of adjuvant TKI for NSCLC in the clinical practice.
辅助酪氨酸激酶抑制剂 (TKI) 在非小细胞肺癌 (NSCLC) 中的作用尚未明确。最近的随机对照试验显示,携带表皮生长因子受体 (EGFR) 突变的患者无病生存期 (DFS) 获益。然而,针对任何 EGFR 状态患者的旧试验并未显示出相同的获益。我们旨在评估 NSCLC 患者辅助 TKI 的疗效和安全性。检索了 Medline(PubMed)和 EMBASE 电子数据库,以寻找相关的随机对照试验。使用随机效应模型。主要结局是通过风险比 (HR) 测量的 DFS。次要结局是通过 HR 测量的总生存期 (OS)、2 年 DFS 和通过风险比和比值比 (OR) 分别表示的毒性。亚组分析评估了试验设计的 DFS。纳入了 6 项包含 1860 名患者的试验。在携带 EGFR 突变的患者中,辅助 TKI 可使疾病复发风险降低 48%(HR:0.52,95%置信区间 [CI]:0.35-0.78),提高 2 年 DFS(HR:0.53,95% CI:0.43-0.66),但不改善 OS(HR:0.64,95% CI:0.22-1.89)。≥3 级皮肤毒性(OR:6.07,95% CI:4.34-8.51)和腹泻(OR:4.05;95% CI:2.44-6.74)的发生风险增加。在亚组分析中,与化疗后使用 TKI 的试验相比,使用 TKI 替代化疗的试验中 DFS 获益更为明显。结论:辅助 TKI 可降低携带 EGFR 突变的 NSCLC 患者的复发风险,但不改善 OS。需要更长时间的随访,以对 OS 进行明确评估,并确定 NSCLC 辅助 TKI 在临床实践中的作用。