The objective of this proposal is to provide new statistical methods, or modifications and clarifications of existing methods, related to the design and analysis of clinical or laboratory cancer studies conducted at the University of Wisconsin or at other cancer centers. Four research areas have been selected: 1. Methods for data monitoring; 2. Design of Phase 1 trials; 3. Analysis of longitudinal data; and 4. Survival analysis. Methods for data monitoring are useful in the proper early termination of trials with evidence for either benefit or harm or if there is little chance of obtaining significant results, thereby saving patient and financial resources. The previous grant has developed and studied group sequential methods as well as stochastic curtailment. The proposal is to further develop ongoing efforts. While Phase I trials are numerous, few statistical design methods are available and the most popular current design has not been fully evaluated. Given that our Cancer Center does numerous Phase I trials, we are interested in more efficient designs in obtaining the maximum tolerated dose, using sequential methods. Some methodological progress has already been achieved in our research. Many epidemiological and clinical trials make repeated measurements of patients overtime, often observing the rate of change. One such case is a pilot prevention trial in Stage I breast cancer evaluating the effect of tamoxifen on bone density and serum lipids. Existing statistical methods range from simple regression to more complex multivariate models. Further evaluation is needed as to the advantages, e.g., robustness and efficiency, of the complex models relative to simple regression. Survival analysis is a central method in biostatistics, especially for clinical research. While models such as the proportional hazards regression are commonly used, methods for verification of the model and diagnostics are needed. Such verification and the impact of various observations is highly desirable in order to have confidence in the analyses. Existing work by the investigators, using methods analogous to other regression techniques, needs to be further developed and software provided. Finally, issues related to the relative efficiency of the Cox proportional hazards model and alternatives to the KaplanMeier will be pursued.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA018332-14
Application #
3164929
Study Section
(SSS)
Project Start
1978-07-01
Project End
1990-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
14
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
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