He Xi-Ran, Han Shu-Yan, Li Ping-Ping
Department of Integration of Traditional Chinese and Western Medicine, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University School of Oncology, Peking University Cancer Hospital and Institute, Beijing 100142, China.
J Cancer Res Ther. 2016 Apr-Jun;12(2):735-43. doi: 10.4103/0973-1482.150411.
The aim was to evaluate the efficacy and safety of Kang' ai (KA) injection for patients with nonsmall cell lung cancer (NSCLC). Furthermore, to identify if more trials are needed before reliable conclusions could be drawn with regard to these outcomes.
We searched the Cochrane library, PubMed, EMBASE, VIP, CBMdisc, and CNKI in September 2012, and then an additional updated search was conducted in January 2013. Only relevant randomized controlled trials (RCTs) on KA injection plus first-line cisplatin-based chemotherapy in the treatment of NSCLC were identified. Trials' data was reviewed and extracted by two reviewers independently. The quality of included studies was assessed according to a statement from Cochrane Handbook. RevMan 5 Software and Trial sequential analysis (TSA) software were applied for data analyses.
A total of 31 RCTs involving 2259 patients were included. The results of meta-analysis showed that compared with chemotherapy alone, the combination of KA injection plus chemotherapy had a statistically significant benefit in improving clinical response rate (relative risk [RR] =1.29, 95% confidence interval [CI]: 1.17-1.41, P < 0.00001), clinical benefit rate (RR = 1.19, 95% CI: 1.14-1.25, P < 0.00001) and quality of life (RR = 1.79, 95% CI: 1.63-1.98, P < 0.00001); hematological toxicity (white blood cell) (RR = 0.71, 95% CI: 0.66-0.76, P < 0.00001) and nonhematological toxicity (nausea and vomiting) (RR = 0.73, 95% CI: 0.65-0.83, P < 0.00001) were improved as well. TSA showed that all cumulative Z-score crossed their monitoring boundaries, demonstrating that no more trials are needed before reliable conclusions could be drawn.
Current evidence presented that KA injection might improve the therapeutic effect when combined with chemotherapy. Moreover, no more trials are needed in future according to TSA. Nevertheless, additional randomized studies investigating KA injection are needed to be further evaluated.
旨在评估康艾(KA)注射液对非小细胞肺癌(NSCLC)患者的疗效和安全性。此外,确定在就这些结果得出可靠结论之前是否需要更多试验。
我们于2012年9月检索了考克兰图书馆、PubMed、EMBASE、维普、中国生物医学文献数据库和中国知网,然后在2013年1月进行了一次更新检索。仅纳入了关于KA注射液联合一线铂类化疗治疗NSCLC的相关随机对照试验(RCT)。试验数据由两名研究者独立审查和提取。根据《考克兰手册》的一份声明评估纳入研究的质量。应用RevMan 5软件和序贯试验分析(TSA)软件进行数据分析。
共纳入31项RCT,涉及2259例患者。荟萃分析结果显示,与单纯化疗相比,KA注射液联合化疗在提高临床缓解率(相对危险度[RR]=1.29,95%置信区间[CI]:1.17 - 1.41,P<0.00001)、临床获益率(RR = 1.19,95%CI:1.14 - 1.25,P<0.00001)和生活质量(RR = 1.79,95%CI:1.63 - 1.98,P<0.00001)方面具有统计学显著益处;血液学毒性(白细胞)(RR = 0.71,95%CI:0.66 - 0.76,P<0.00001)和非血液学毒性(恶心和呕吐)(RR = 0.73,95%CI:0.65 - 0.83,P<0.00001)也有所改善。TSA显示所有累积Z值均越过其监测边界,表明在得出可靠结论之前无需更多试验。
当前证据表明KA注射液联合化疗可能提高治疗效果。此外,根据TSA,未来无需更多试验。然而,仍需要更多关于KA注射液的随机研究进行进一步评估。