Grant Details
Grant Number: |
1R03CA212799-01 Interpret this number |
Primary Investigator: |
Wang, Molin |
Organization: |
Harvard School Of Public Health |
Project Title: |
Statistical Methods for Analysis of Pooled Continuous Biomarker Data Arisen From Multiple Studies |
Fiscal Year: |
2017 |
Abstract
Project Summary / Abstract
Increasingly, multiple studies relating biomarkers to cancer and other health outcomes are pooled to obtain an
overall risk profile, and a major challenge of pooling biomarker data is potential sources of variability of the
biomarker data, including assay and laboratory variability. Currently there are no reliable and well-evaluated
statistical methods to conduct the aggregated analysis for pooled biomarker data while taking care of the
calibration process that correct for the between-study biomarker variability. In this proposal, we will develop
efficient statistical methods for incorporating the calibration process in the aggregated data analysis. User-
friendly software implementing the methods will be made publicly available. In addition, analysis results have
potential to be substantially different between using the two commonly used methods for analyzing pooled
data, the two-stage analysis method and the aggregated data analysis method, and in the two-stage method,
between the fixed effect model method and the random effect model method. Investigators conducting
consortial research are confronted with the choice between the methods. We will compare these methods such
that the choices of analysis methods will be made to exploit the full power of the data available to maximize the
information gained, while at the same time only making minimum and realistic assumptions.
Publications
Spline Analysis of Biomarker Data Pooled from Multiple Matched/Nested Case-Control Studies.
Authors: Wu Y.
, Gail M.
, Smith-Warner S.
, Ziegler R.
, Wang M.
.
Source: Cancers, 2022-06-03 00:00:00.0; 14(11), .
EPub date: 2022-06-03 00:00:00.0.
PMID: 35681763
Related Citations
A repeated measures approach to pooled and calibrated biomarker data.
Authors: Sloan A.
, Cheng C.
, Rosner B.
, Ziegler R.G.
, Smith-Warner S.A.
, Wang M.
.
Source: Biometrics, 2021-12-30 00:00:00.0; , .
EPub date: 2021-12-30 00:00:00.0.
PMID: 34967001
Related Citations
Extent, impact, and mitigation of batch effects in tumor biomarker studies using tissue microarrays.
Authors: Stopsack K.H.
, Tyekucheva S.
, Wang M.
, Gerke T.A.
, Vaselkiv J.B.
, Penney K.L.
, Kantoff P.W.
, Finn S.P.
, Fiorentino M.
, Loda M.
, et al.
.
Source: Elife, 2021-12-23 00:00:00.0; 10, .
EPub date: 2021-12-23 00:00:00.0.
PMID: 34939926
Related Citations
Statistical methods for analysis of combined biomarker data from multiple nested case-control studies.
Authors: Cheng C.
, Sloan A.
, Wang M.
.
Source: Statistical Methods In Medical Research, 2021 Aug; 30(8), p. 1944-1959.
EPub date: 2021-07-07 00:00:00.0.
PMID: 34232834
Related Citations
STATISTICAL METHODS FOR ANALYSIS OF COMBINED CATEGORICAL BIOMARKER DATA FROM MULTIPLE STUDIES.
Authors: Cheng C.
, Wang M.
.
Source: The Annals Of Applied Statistics, 2020 Sep; 14(3), p. 1146-1163.
EPub date: 2020-09-18 00:00:00.0.
PMID: 33633815
Related Citations
Statistical methods for biomarker data pooled from multiple nested case-control studies.
Authors: Sloan A.
, Smith-Warner S.A.
, Ziegler R.G.
, Wang M.
.
Source: Biostatistics (oxford, England), 2019-11-21 00:00:00.0; , .
EPub date: 2019-11-21 00:00:00.0.
PMID: 31750898
Related Citations
Design and analysis considerations for combining data from multiple biomarker studies.
Authors: Sloan A.
, Song Y.
, Gail M.H.
, Betensky R.
, Rosner B.
, Ziegler R.G.
, Smith-Warner S.A.
, Wang M.
.
Source: Statistics In Medicine, 2019-04-15 00:00:00.0; 38(8), p. 1303-1320.
EPub date: 2018-12-19 00:00:00.0.
PMID: 30569596
Related Citations