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. 2011 May 20;14(5):404–413. [Article in Chinese] doi: 10.3779/j.issn.1009-3419.2011.05.05

3.

纳入研究的干预措施及结局指标

Inventions and endpoint of included trials

Study Invention group Case Endpoint
Experimental Control Experimental Control
NPE: Vinorelbine+Oxaliplatin+rh-endostatin; NOE: Vinorelbine+Oxaliplatin+rh-endostatin; GPE: Gemcitabine+Cisplatin+rh-endostatin; TCE: Paclitaxel+Carboplatin+rh-endostatin; NP: Vinorelbine+Oxaliplatin; NO: Vinorelbine+Oxaliplatin; GP: Gemcitabine+Cisplatin; TC: Paclitaxel +Carboplatin; T: Paclitaxel; RT: radiotherapy; RR: response rate; SI:symptom improvement.
Yang L[23] NPE NP 54 33 RR, SI, Adverse reactions
Wang JW[20] NPE NP+placebo 322 164 RR, SI, Adverse reactions
Huang C[18] NPE NP 50 24 RR, Survival rate, Adverse reactions
Chen SJ[10] NOE NO 24 26 RR, Adverse reactions
Huang GS[7] NPE NP 20 20 RR, Survival rate, SI, Adverse reactions
Fan QL[22] NPE NP 20 20 RR, Adverse reactions
Cai L[13] NPE NP 39 32 RR, Survival rate, SI, Adverse reactions
XieYR[9] GPE GP 22 26 RR, Survival rate, SI, Adverse reactions
Liu J[16] NPE+RT NP+RT 31 31 RR, Survival rate, Adverse reactions
Ma JB[21] NPE+RT NP+RT 23 23 RR, Survival rate, SI, Adverse reactions
Zhang T[14] GPE T 48 56 RR, SI, Adverse reactions
Tang Z[8] TCE TC 27 26 RR, Adverse reactions
Han LC[11] TPE TP 37 31 RR, Adverse reactions
Jin J[12] NPE NP 15 25 RR, Survival rate, Adverse reactions
Liu J[15] TE T 30 30 RR, Adverse reactions