Using a surrogate marker for early testing of a treatment effect
The development of methods to identify, validate, and use surrogate markers to test for a treatment effect has been an area of intense research interest given the potential for valid surrogate markers to reduce the required costs and follow-up times of future studies. Several quantities and procedur...
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Published in | Biometrics Vol. 75; no. 4; pp. 1253 - 1263 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Periodicals, Inc
01.12.2019
Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 0006-341X 1541-0420 1541-0420 |
DOI | 10.1111/biom.13067 |
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Summary: | The development of methods to identify, validate, and use surrogate markers to test for a treatment effect has been an area of intense research interest given the potential for valid surrogate markers to reduce the required costs and follow-up times of future studies. Several quantities and procedures have been proposed to assess the utility of a surrogate marker. However, few methods have been proposed to address how one might use the surrogate marker information to test for a treatment effect at an earlier time point, especially in settings where the primary outcome and the surrogate marker are subject to censoring. In this paper, we propose a novel test statistic to test for a treatment effect using surrogate marker information measured prior to the end of the study in a timeto-event outcome setting. We propose a robust nonparametric estimation procedure and propose inference procedures. In addition, we evaluate the power for the design of a future study based on surrogate marker information. We illustrate the proposed procedure and relative power of the proposed test compared to a test performed at the end of the study using simulation studies and an application to data from the Diabetes Prevention Program. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0006-341X 1541-0420 1541-0420 |
DOI: | 10.1111/biom.13067 |