Zhang Yaxiong, Zhang Zhonghan, Huang Xiaodan, Kang Shiyang, Chen Gang, Wu Manli, Miao Siyu, Huang Yan, Zhao Hongyun, Zhang Li
Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China; State Key Laboratory of Oncology in South China, Guangzhou, China; Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China; State Key Laboratory of Oncology in South China, Guangzhou, China; Collaborative Innovation Center for Cancer Medicine, Guangzhou, China; Zhongshan School of Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Clin Lung Cancer. 2017 Sep;18(5):e333-e340. doi: 10.1016/j.cllc.2016.09.006. Epub 2016 Oct 27.
Five major first- and second-generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), including erlotinib, gefitinib, icotinib, afatinib, and dacomitinib, are currently optional for patients with advanced non-small-cell lung cancer (NSCLC) who harbor EGFR mutations. However, there was no head-to-head-based network meta-analysis among all the TKIs in EGFR-mutated populations.
Eligible literature was searched from an electronic database. Data of objective response rate, disease control rate, progression-free survival, and overall survival were extracted from enrolled studies. Multiple treatment comparisons based on Bayesian network integrated the efficacy of all included treatments.
Six phase III randomized trials involving 1055 EGFR-mutated patients with advanced NSCLC were enrolled. Multiple treatment comparisons showed that 5 different EGFR-TKIs shared equivalent therapeutic efficacy in terms of all outcome measures. Rank probabilities indicated that dacomitinib and afatinib had potentially better efficacy compared with erlotinib, gefitinib, and icotinib in the EGFR-mutated patients. When compared with other agents, potential survival benefits (progression-free and overall survival) were observed in dacomitinib, whereas afatinib showed a better rank probability in overall response rate and disease control rate.
Our study indicated a preferable therapeutic efficacy in the second-generation TKIs (dacomitinib and afatinib) when compared with the first-generation TKIs (erlotinib, gefitinib, and icotinib).
包括厄洛替尼、吉非替尼、埃克替尼、阿法替尼和达可替尼在内的五种主要的第一代和第二代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs),目前是表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)患者的可选治疗药物。然而,在EGFR突变人群中,尚未对所有这些酪氨酸激酶抑制剂进行基于直接比较的网状Meta分析。
从电子数据库中检索符合条件的文献。从纳入的研究中提取客观缓解率、疾病控制率、无进展生存期和总生存期的数据。基于贝叶斯网络的多种治疗比较整合了所有纳入治疗的疗效。
纳入了六项涉及1055例EGFR突变的晚期NSCLC患者的III期随机试验。多种治疗比较显示,5种不同的EGFR-TKIs在所有疗效指标方面具有相当的治疗效果。排序概率表明,在EGFR突变患者中,与厄洛替尼、吉非替尼和埃克替尼相比,达可替尼和阿法替尼可能具有更好的疗效。与其他药物相比,达可替尼观察到潜在的生存获益(无进展生存期和总生存期),而阿法替尼在总缓解率和疾病控制率方面显示出更好的排序概率。
我们的研究表明,与第一代酪氨酸激酶抑制剂(厄洛替尼、吉非替尼和埃克替尼)相比,第二代酪氨酸激酶抑制剂(达可替尼和阿法替尼)具有更好的治疗效果。