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. Author manuscript; available in PMC: 2014 Sep 22.
Published in final edited form as: Cochrane Database Syst Rev. 2012 May 16;5:CD007583. doi: 10.1002/14651858.CD007583.pub3
OUTCOMES
Progression-free survival
If the following were reported, record the value Value Relevant supporting text and location. (page/column/paragraph)
Unadjusted hazard ratio (HR)
Was the comparison group the reference group for the estimate of the HR?
Yes/No/Unclear
95% confidence on unadjusted HR
Lower 95% confidence interval
Upper 95% confidence interval
Adjusted hazard ratio (HR)
Was the comparison group the reference group for the estimate of the HR?
List the factors for which the HR was adjusted:
Yes/No/Unclear
95% confidence on adjusted HR
Lower 95% confidence interval
Upper 95% confidence interval
If an HR was reported, record the number of women in each treatment arm on whom the estimated HR was based:
Number of women in intervention arm:
Number of women in comparison arm:
If an HR was reported, and if the study was based on a pre-specified protocol for assigning women to intervention group or comparison group, was the HR based on an intention-to-treat (ITT) analysis? That is, were women analysed in the groups to which they were assigned, regardless of what treatment they received? Yes/No/Unclear
SE(HR)
SE(ln(HR))
Var(HR)
Var(ln(HR))
Kaplan Meier plots Yes/No
Minimum follow up time
Maximum follow up time
Log rank P-value
Was Cox regression reported? Yes/No
Cox P-value