Clinical trials with rare or distant outcomes are usually designed to be large in size and long term. The resource-demand and time-consuming characteristics limit the feasibility and efficiency of the studies. There are motivations to replace rare or distal clinical endpoints by reliable surrogate markers, which could be earlier and easier to collect. However, statistical challenges still exist to evaluate and rank potential surrogate markers. In this paper, we define a generalized proportion of treatment effect for survival settings. The measure’s definition and estimation do not rely on any model assumption. It is equipped with a consistent and asymptotically normal non-parametric estimator. Under proper conditions, the measure reflects t...
Ideal tests of the effects of therapeutic interventions measure the desired outcomes; however, the d...
Summary. Frangakis and Rubin (2002, Biometrics 58, 21–29) proposed a new definition of a surrogate e...
Part of the recent literature on the validation of biomarkers as surrogate endpoints proposes to und...
Given the long follow-up periods that are often required for treatment or intervention studies, the ...
Randomized clinical trials with rare primary endpoints or long duration times are costly. Because of...
When evaluating the effectiveness of a treatment, policy, or intervention, the desired measure of ef...
Randomized clinical trials with rare primary endpoints or long duration times are costly. Because of...
When evaluating the effectiveness of a treatment, policy, or intervention, the desired measure of ef...
A surrogate endpoint is intended to replace a clinical endpoint for the evaluation of new treatments...
Motivated by increasing pressure for decision makers to shorten the time required to evaluate the ef...
Thesis (Ph.D.)--Boston UniversityPLEASE NOTE: Boston University Libraries did not receive an Authori...
The evaluation of surrogate endpoints is thought to be first studied by Prentice, who presented a de...
In many clinical settings, improving patient survival is of interest but a practical surrogate, such...
Semicompeting risk outcome data (e.g., time to disease progression and time to death) are commonly c...
BACKGROUND: A surrogate marker is a variable commonly used in clinical trials to guide treatment dec...
Ideal tests of the effects of therapeutic interventions measure the desired outcomes; however, the d...
Summary. Frangakis and Rubin (2002, Biometrics 58, 21–29) proposed a new definition of a surrogate e...
Part of the recent literature on the validation of biomarkers as surrogate endpoints proposes to und...
Given the long follow-up periods that are often required for treatment or intervention studies, the ...
Randomized clinical trials with rare primary endpoints or long duration times are costly. Because of...
When evaluating the effectiveness of a treatment, policy, or intervention, the desired measure of ef...
Randomized clinical trials with rare primary endpoints or long duration times are costly. Because of...
When evaluating the effectiveness of a treatment, policy, or intervention, the desired measure of ef...
A surrogate endpoint is intended to replace a clinical endpoint for the evaluation of new treatments...
Motivated by increasing pressure for decision makers to shorten the time required to evaluate the ef...
Thesis (Ph.D.)--Boston UniversityPLEASE NOTE: Boston University Libraries did not receive an Authori...
The evaluation of surrogate endpoints is thought to be first studied by Prentice, who presented a de...
In many clinical settings, improving patient survival is of interest but a practical surrogate, such...
Semicompeting risk outcome data (e.g., time to disease progression and time to death) are commonly c...
BACKGROUND: A surrogate marker is a variable commonly used in clinical trials to guide treatment dec...
Ideal tests of the effects of therapeutic interventions measure the desired outcomes; however, the d...
Summary. Frangakis and Rubin (2002, Biometrics 58, 21–29) proposed a new definition of a surrogate e...
Part of the recent literature on the validation of biomarkers as surrogate endpoints proposes to und...