Volume 73, Issue 2
BIOMETRIC PRACTICE

Testing violations of the exponential assumption in cancer clinical trials with survival endpoints

Gang Han

Corresponding Author

E-mail address: ghan@sph.tamhsc.edu

Department of Epidemiology and Biostatistics, School of Public Health, Texas A&M University, 212 Adriance Lab Road, College Station, Texas 77843, U.S.A.

email: ghan@sph.tamhsc.eduSearch for more papers by this author
Michael J. Schell

The Biostatistics and Bioinformatics Department, H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, Florida, 33612 U.S.A.

Oncologic Sciences, University of South Florida, 4202 E. Fowler Ave Tampa, Florida, 33620 U.S.A.

Search for more papers by this author
Heping Zhang

Department of Biostatistics, Yale University School of Public Health, 60 College Street, New Haven, Connecticut, 06520 U.S.A.

Search for more papers by this author
Daniel Zelterman

Department of Biostatistics, Yale University School of Public Health, 60 College Street, New Haven, Connecticut, 06520 U.S.A.

Search for more papers by this author
Lajos Pusztai

Yale Comprehensive Cancer Center, Yale School of Medicine, 333 Cedar Street, New Haven, Connecticut, 06520 U.S.A.

Search for more papers by this author
Kerin Adelson

Yale Comprehensive Cancer Center, Yale School of Medicine, 333 Cedar Street, New Haven, Connecticut, 06520 U.S.A.

Search for more papers by this author
Christos Hatzis

Yale Comprehensive Cancer Center, Yale School of Medicine, 333 Cedar Street, New Haven, Connecticut, 06520 U.S.A.

Search for more papers by this author
First published: 26 September 2016
Citations: 3

Summary

Personalized cancer therapy requires clinical trials with smaller sample sizes compared to trials involving unselected populations that have not been divided into biomarker subgroups. The use of exponential survival modeling for survival endpoints has the potential of gaining 35% efficiency or saving 28% required sample size (Miller, 1983), making personalized therapy trials more feasible. However, the use of exponential survival has not been fully accepted in cancer research practice due to uncertainty about whether or not the exponential assumption holds. We propose a test for identifying violations of the exponential assumption using a reduced piecewise exponential approach. Compared with an alternative goodness‐of‐fit test, which suffers from inflation of type I error rate under various censoring mechanisms, the proposed test maintains the correct type I error rate. We conduct power analysis using simulated data based on different types of cancer survival distribution in the SEER registry database, and demonstrate the implementation of this approach in existing cancer clinical trials.

Number of times cited according to CrossRef: 3

  • Trends in the Price per Median and Mean Life-Year Gained Among Newly Approved Cancer Therapies 1995 to 2017, Value in Health, 10.1016/j.jval.2019.08.005, (2019).
  • The changing face of clinical trials in the personalized medicine and immuno-oncology era: report from the international congress on clinical trials in Oncology & Hemato-Oncology (ICTO 2017), Journal of Experimental & Clinical Cancer Research, 10.1186/s13046-017-0668-0, 36, 1, (2017).
  • Designing historical control studies with survival endpoints using exact statistical inference, Pharmaceutical Statistics, 10.1002/pst.2050, 0, 0, (undefined).

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.