Efficacy and safety of EFGR tyrosine kinase inhibitor monotherapy with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer:a Meta-analysis
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Efficacy and safety of EFGR tyrosine kinase inhibitor monotherapy with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer:a Meta-analysis
Journal of Chongqing Medical UniversityVol. 41, Issue 9, Pages: 959-963(2016)
Yang Yingqing, Jiang Depeng, Jiang Youfan. Efficacy and safety of EFGR tyrosine kinase inhibitor monotherapy with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer:a Meta-analysis. [J]. Journal of Chongqing Medical University 41(9):959-963(2016)
Yang Yingqing, Jiang Depeng, Jiang Youfan. Efficacy and safety of EFGR tyrosine kinase inhibitor monotherapy with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer:a Meta-analysis. [J]. Journal of Chongqing Medical University 41(9):959-963(2016) DOI: 10.13406/j.cnki.cyxb.000949.
Efficacy and safety of EFGR tyrosine kinase inhibitor monotherapy with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer:a Meta-analysis
Objective:To systematically evaluate the efficacy and safety of epidermal growth factor receptor tyrosine kinase inhibitor monotherapy(gefitinib or erlotinib)with docetaxel monotherapy in previously treated advanced non-small-cell lung cancer(NSCLC).Methods:Pub Med
Embase
Cochrane library
CNKI
Wan-fang Data and VIP were searched to collect randomized clinical trials(RCTs)comparing EGFR-TKI monotherapy with docetaxel chemotherapy in previously treated advanced NSCLC. The hazard ratio(HR)or odds ratio(OR)
with their corresponding 95% confidence intervals(CI)were pooled using Review manager 5.3.0. Results:Six randomized controlled trials involving 2747patients(EGFR-TKI 1389 patients
docetaxel 1358 patients)were eligible. The pooled HRs showed no significant difference in OS(HR=0.90
95%CI=0.78 to 1.04
Z=1.40
P=0.16). PFS was elongated in docetaxel group than in erlotinib group(HR=1.31
95%CI=1.11 to 1.54
Z=3.24
P=0.001). There was no difference in PFS between docetaxel group and gentitinib group(HR=0.90
95%CI=0.78 to 1.04
Z=1.40
P=0.16). Safety analysis showed that incidence of side effect at grade 3 or 4 was low in EGFR-TKI group;the side effects included neutropeni(RR=0.06
95%CI=0.04 to 0.08)
febrile
neutropenia(RR =0.09
95% CI =0.05 to 0.16)
and nurotoxicity(RR=0.25
995%CI=0.05 to 0.16). The incidence of rash at grade3 or 4 was increased(RR=15.03
95%CI=5.81 to 38.88). Conclusion:Although having similar OS and PFS