Xu Yu-Qiong, Long Xiang, Han Ming, Huang Ming-Qiang, Lu Jia-Fa, Sun Xue-Dong, Han Wei
Department of Emergency Medicine, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen 518000, Guangdong Province, China.
Department of Respiratory and Critical Care Medicine, Peking University Shenzhen Hospital, Shenzhen 518000, Guangdong Province, China.
World J Clin Cases. 2021 Jan 26;9(3):581-601. doi: 10.12998/wjcc.v9.i3.581.
Lung cancer is a major cause of death among patients, and non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancers in many countries.
To evaluate the clinical benefit (CB) of COX-2 inhibitors in patients with advanced NSCLC using systematic review.
We searched the six electronic databases up until December 9, 2019 for studies that examined the efficacy and safety of the addition of COX-2 inhibitors to chemotherapy for NSCLC. Overall survival (OS), progression free survival (PFS), 1-year survival rate (SR), overall response rate (ORR), CB, complete response (CR), partial response (PR), stable disease (SD), and toxicities were measured with more than one outcome as their endpoints. Fixed and random effects models were used to calculate risk estimates in a meta-analysis. Potential publication bias was calculated using Egger's linear regression test. Data analysis was performed using R software.
The COX-2 inhibitors combined with chemotherapy were not found to be more effective than chemotherapy alone in OS, progression free survival, 1-year SR, CB, CR, and SD. However, there was a difference in overall response rate for patients with advanced NSCLC. In a subgroup analysis, significantly increased ORR results were found for celecoxib, rofecoxib, first-line treatment, and PR. For adverse events, the increase in COX-2 inhibitor was positively correlated with the increase in grade 3 and 4 toxicity of leukopenia, thrombocytopenia, and cardiovascular events.
COX-2 inhibitor combined with chemotherapy increased the total effective rate of advanced NSCLC with the possible increased risk of blood toxicity and cardiovascular events and had no effect on survival index.
肺癌是患者死亡的主要原因,在许多国家,非小细胞肺癌(NSCLC)占所有肺癌的80%以上。
通过系统评价评估COX-2抑制剂对晚期NSCLC患者的临床获益(CB)。
我们检索了截至2019年12月9日的六个电子数据库,以查找研究COX-2抑制剂联合化疗治疗NSCLC的疗效和安全性的研究。以总生存期(OS)、无进展生存期(PFS)、1年生存率(SR)、总缓解率(ORR)、CB、完全缓解(CR)、部分缓解(PR)、疾病稳定(SD)和毒性为终点,测量多个结局指标。在荟萃分析中使用固定效应模型和随机效应模型计算风险估计值。使用Egger线性回归检验计算潜在的发表偏倚。使用R软件进行数据分析。
未发现COX-2抑制剂联合化疗在OS、无进展生存期、1年SR、CB、CR和SD方面比单纯化疗更有效。然而,晚期NSCLC患者的总缓解率存在差异。在亚组分析中,发现塞来昔布、罗非昔布、一线治疗和PR的ORR结果显著增加。对于不良事件,COX-2抑制剂的增加与白细胞减少、血小板减少和心血管事件的3级和4级毒性增加呈正相关。
COX-2抑制剂联合化疗提高了晚期NSCLC的总有效率,但可能增加血液毒性和心血管事件的风险,且对生存指标无影响。