Zhou Jian-Guo, Tian Xu, Cheng Long, Zhou Quan, Liu Yuan, Zhang Yu, Bai Yu-Ju, Ma Hu
From the Department of Oncology, Affiliated Hospital of Zunyi Medical University (JGZ, LC,YZ,YJB, HM); Center for Translational Medicine, Zunyi Medical University, Zunyi (JGZ, HM); Graduate College (XT); School of Nursing, Tianjin University of Traditional Chinese Medicine, Tianjin (XT); Department of Science and Education, First People's Hospital of Changde City, Changde (QZ); Department of Pharmacology (YL); and Key Laboratory of Basic Pharmacology of Ministry of Education, Zunyi Medical University, Zunyi, China (YL).
Medicine (Baltimore). 2015 Oct;94(40):e1719. doi: 10.1097/MD.0000000000001719.
Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are a critical member of systemic therapy for advanced non-small-cell lung cancer (NSCLC). Erlotinib is the first-generation EGFR-TKIs, the National Comprehensive Cancer Network (NCCN) guidelines recommend it as a first-line agent in patients with sensitizing EGFR mutations. However, the safety of erlotinib plus chemotherapy (CT) or erlotinib alone for advanced NSCLC remains controversial. We carried out a systematic meta-analysis to determine the overall risk of neutropenia and leukopenia associated with erlotinib. PubMed, EMBASE, CBM, CNKI, WanFang database, The Cochrane library, Web of Science, as well as abstracts presented at ASCO conferences and ClinicalTrials.gov were searched to identify relevant studies. RR with 95% CIs for neutropenia and leukopenia were all extracted. The random-effects model was used to calculate pooled RRs and 95% CIs. Power calculation was performed using macro embedded in SAS software after all syntheses were conducted. We identified 12 eligible studies involving 3932 patients. Erlotinib plus CT or alone relative to CT is associated with significantly decreased risks of neutropenia and leukopenia in patients with advanced NSCLC (RR, 0.38; 95% CI, 0.21-0.71; P = 0.00; incidence: 9.9 vs. 35.2%) and (RR, 0.32; 95% CI, 0.11-0.93; P = 0.04; incidence: 3.5 vs. 11.6%), respectively. The subgroup analysis by erlotinib with or without CT showed that erlotinib combine with CT have no significance decrease the relative risks of neutropenia or leukopenia (RR, 0.98; 95% CI, 0.78-1.23; P = 0.87; incidence: 26.2 vs. 30.5%) and (RR, 0.81; 95% CI, 0.34-1.95; P = 0.64; incidence: 6.5 vs. 9.3%), respectively. However, erlotinib alone could decrease incidence of neutropenia (RR, 0.14; 95% CI, 0.07-0.27; P = 0.00; incidence: 3.7 vs. 40.8%) or leukopenia (RR, 0.07; 95% CI, 0.01-0.45; P = 0.01; incidence: 0.8 vs. 15.7%). The power analysis suggests that a power of 61.31% was determined to detect an RR of 0.38 for neutropenia, and 78.03% for an RR of 0.32 for leukopenia. The present meta-analysis suggested that erlotinib could decrease the incidence of neutropenia and leukopenia in patients with advanced NSCLC undergoing erlotinib regardless of whether combined with CT or not. The subgroup analysis revealed that erlotinib combine with CT did not affect the incidence; however, erlotinib alone could significantly decrease the incidence of neutropenia and leukopenia compared with CT alone.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)是晚期非小细胞肺癌(NSCLC)全身治疗的关键成员。厄洛替尼是第一代EGFR-TKIs,美国国立综合癌症网络(NCCN)指南推荐其作为具有敏感EGFR突变患者的一线用药。然而,厄洛替尼联合化疗(CT)或单独使用厄洛替尼治疗晚期NSCLC的安全性仍存在争议。我们进行了一项系统的荟萃分析,以确定与厄洛替尼相关的中性粒细胞减少和白细胞减少的总体风险。检索了PubMed、EMBASE、CBM、CNKI、万方数据库、考克兰图书馆、科学网,以及美国临床肿瘤学会(ASCO)会议上发表的摘要和ClinicalTrials.gov,以识别相关研究。提取了中性粒细胞减少和白细胞减少的RR及95%可信区间(CI)。采用随机效应模型计算合并RR及95%CI。在所有分析完成后,使用SAS软件中嵌入的宏进行效能计算。我们确定了12项符合条件的研究,涉及3932例患者。与CT相比,厄洛替尼联合CT或单独使用厄洛替尼可使晚期NSCLC患者中性粒细胞减少和白细胞减少的风险显著降低(RR为0.38;95%CI为0.21-0.71;P = 0.00;发生率:9.9%对35.2%)以及(RR为0.32;95%CI为0.11-0.93;P = 0.04;发生率:3.5%对11.6%)。按是否联合CT对厄洛替尼进行亚组分析显示,厄洛替尼联合CT对中性粒细胞减少或白细胞减少的相对风险无显著降低(RR为0.98;95%CI为0.78-1.23;P = 0.87;发生率:26.2%对30.5%)以及(RR为0.81;95%CI为0.34-1.95;P = 0.64;发生率:6.5%对9.3%)。然而,单独使用厄洛替尼可降低中性粒细胞减少的发生率(RR为0.14;95%CI为0.07-0.27;P = 0.00;发生率:3.7%对40.8%)或白细胞减少的发生率(RR为0.07;95%CI为0.01-0.45;P = 0.01;发生率:0.8%对15.7%)。效能分析表明,检测中性粒细胞减少RR为0.38时的效能为61.31%,检测白细胞减少RR为0.32时的效能为78.03%。本荟萃分析表明,无论是否联合CT,厄洛替尼均可降低接受厄洛替尼治疗的晚期NSCLC患者中性粒细胞减少和白细胞减少的发生率。亚组分析显示,厄洛替尼联合CT不影响发生率;然而,与单独使用CT相比,单独使用厄洛替尼可显著降低中性粒细胞减少和白细胞减少的发生率。