摘要:The Fleming-Harrington and constant piecewise wei- ghted logrank tests for late effects in clinical trials are considered. Both tests depend on a parameter ($q$ for the Fleming-Harrington and $t^{*}$ for the constant piecewise weighted logrank) that has to be chosen before the trial analysis. The problem of choosing the most appropriate test and associated parameter value for a given trial is addressed. For this purpose, the tests are compared in terms of their sensitivity to $q$ and $t^{*}$ and of their asymptotic relative efficiency and necessary sample size. Some guidelines for choosing the most appropriate weight for testing late effects are provided. The methodology is illustrated on a medical dataset.