Cial events such as CR and PR, it surpassed other targeted drugs 
in maintaining the pharmacodynamic effect. This finding was consistent with the mechanism of bevacizumab which was slowing down the vessel growth BIBS39 instead of causing cell death. As we can see in figure 5, several trials with treatment group applying bevacizumab (marked in red) fall below the regression line, indicating that there are other factors contributing to the prolongation of PFS in spite of the elevation of ORR. The contribution of SD in PFS time is greater in the treatment group than in the control group. We presented three primary measures (ORR, PFS and OS) to show the treatment effect of different targeted drugs. Response rate is greatly affected by the original volume of the solid tumor, average duration of administration, and the clinical stage of patients, while PFS and OS time can be greatly affected by the frequency of follow-up. These are possible reasons of having only one clinical trial (E4599) with significant overall survival benefit. Another possible reason of the negative findings in overall survival time may be the low power to detect significance due to small valid sample size. Simple meta-regression in this study showed significantly positive correlation between ln(HROS) and ln(HRPFS) ?in both chemotherapy-naive and previously treated patients, indicating that given a clear benefit in PFS, benefit in OS is much likely to be detected with a larger sample size (figure 5). In other words, we can eliminate the accelerated growth of tumor cells after disease progression which would result in a clear benefit in PFS but not in OS. Our finding that the crude but not the adjusted HROS of bevacizumab was significantly lower than that ?of other three drugs in chemotherapy-naive Lixisenatide site patients indicated that 11967625 ?the advantage in chemotherapy-naive patients was mainly attributed to the elevation of ORR and prolongation of PFS. The finding that neither crude HROS nor adjusted HROS of bevacizumab was significantly different from those of other targeted drugs in previously treated patients may be explained by the complex 
and severity of patients. Selection of target is essential in targeted therapies; therefore whether EGFR is mutated or not is of great significance in clinical decision. However, a considerable number of patients are unable to provide adequate tissue samples for accurate genotyping in practice. Our study showed that the benefit from bevacizumab was independent of EGFR status among a relatively large number of patients especially for those of first-line treatment. Such an effect was not able to detect for patients in second-line or third-line treatment, which suggests that patients may be more likely to show better response to the anti-angiogenic drug at early stage. Based on these findings, we would recommend early use of bevacizumab. Limitations exist in this study. First, our meta-analysis cohort is heterogeneous regarding chemotherapies of the controls, and this may lead to unreliable findings. To address this issue, weperformed an imputation study with leave-one-out strategy. The imputation analysis showed that the results had only slight difference when any single trial was removed from the metaanalysis, which indicates robustness of our study. Secondly, our analysis included a number of steps to minimize the potential for publication bias, including the Begg’s test and Egger’s test. The symmetrical distributions presented in Funnel plot showed a smal.Cial events such as CR and PR, it surpassed other targeted drugs in maintaining the pharmacodynamic effect. This finding was consistent with the mechanism of bevacizumab which was slowing down the vessel growth instead of causing cell death. As we can see in figure 5, several trials with treatment group applying bevacizumab (marked in red) fall below the regression line, indicating that there are other factors contributing to the prolongation of PFS in spite of the elevation of ORR. The contribution of SD in PFS time is greater in the treatment group than in the control group. We presented three primary measures (ORR, PFS and OS) to show the treatment effect of different targeted drugs. Response rate is greatly affected by the original volume of the solid tumor, average duration of administration, and the clinical stage of patients, while PFS and OS time can be greatly affected by the frequency of follow-up. These are possible reasons of having only one clinical trial (E4599) with significant overall survival benefit. Another possible reason of the negative findings in overall survival time may be the low power to detect significance due to small valid sample size. Simple meta-regression in this study showed significantly positive correlation between ln(HROS) and ln(HRPFS) ?in both chemotherapy-naive and previously treated patients, indicating that given a clear benefit in PFS, benefit in OS is much likely to be detected with a larger sample size (figure 5). In other words, we can eliminate the accelerated growth of tumor cells after disease progression which would result in a clear benefit in PFS but not in OS. Our finding that the crude but not the adjusted HROS of bevacizumab was significantly lower than that ?of other three drugs in chemotherapy-naive patients indicated that 11967625 ?the advantage in chemotherapy-naive patients was mainly attributed to the elevation of ORR and prolongation of PFS. The finding that neither crude HROS nor adjusted HROS of bevacizumab was significantly different from those of other targeted drugs in previously treated patients may be explained by the complex and severity of patients. Selection of target is essential in targeted therapies; therefore whether EGFR is mutated or not is of great significance in clinical decision. However, a considerable number of patients are unable to provide adequate tissue samples for accurate genotyping in practice. Our study showed that the benefit from bevacizumab was independent of EGFR status among a relatively large number of patients especially for those of first-line treatment. Such an effect was not able to detect for patients in second-line or third-line treatment, which suggests that patients may be more likely to show better response to the anti-angiogenic drug at early stage. Based on these findings, we would recommend early use of bevacizumab. Limitations exist in this study. First, our meta-analysis cohort is heterogeneous regarding chemotherapies of the controls, and this may lead to unreliable findings. To address this issue, weperformed an imputation study with leave-one-out strategy. The imputation analysis showed that the results had only slight difference when any single trial was removed from the metaanalysis, which indicates robustness of our study. Secondly, our analysis included a number of steps to minimize the potential for publication bias, including the Begg’s test and Egger’s test. The symmetrical distributions presented in Funnel plot showed a smal.
