Copyright
©The Author(s) 2021.
World J Gastrointest Oncol. Nov 15, 2021; 13(11): 1799-1812
Published online Nov 15, 2021. doi: 10.4251/wjgo.v13.i11.1799
Published online Nov 15, 2021. doi: 10.4251/wjgo.v13.i11.1799
Ref. | Entry | Judgement | Support for judgement | |
Li et al[13] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Chen et al[14] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Guler et al[18] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Junca et al[12] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analysesconsistent with a priori plan | |
Tao et al[15] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants in the supplementary materials | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants in the supplementary materials | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Cristiano et al[19] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Li et al[17] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Qu et al[16] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Low risk | Pre-registered protocol available (NCC201709011) | |
Cai et al[11] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Wan et al[9] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Jensen et al[20] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Nunes et al[21] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | No information | No information about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | No information | No information about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan | |
Perrone et al[22] | A | Bias due to confounding | Low risk | No confounding factors |
B | Bias in selection of participants into the study | Low risk | Information provided about the start of follow up and intervention for the participants | |
C | Bias in classification of interventions | Low risk | Information provided about the start of follow up and intervention for the participants | |
D | Bias due to deviationsfrom intended interventions | Low risk | No deviations from the planned interventions | |
E | Bias due to missing data | Low risk | All data were reported | |
F | Bias in measurement of outcomes | Low risk | Comparable methods of outcome assessment in the groups, intervention received in each group unlikely to influence the outcome measure, any error in measuring the outcome is unrelated to intervention | |
G | Bias in selection of the reported result | Moderate risk | No pre-registered protocol available; outcome measurements and analyses consistent with a priori plan |
- Citation: Uhe I, Hagen ME, Ris F, Meyer J, Toso C, Douissard J. Cell-free DNA liquid biopsy for early detection of gastrointestinal cancers: A systematic review. World J Gastrointest Oncol 2021; 13(11): 1799-1812
- URL: https://www.wjgnet.com/1948-5204/full/v13/i11/1799.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v13.i11.1799