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Byar, D.P. (1980) The Veterans Administration Study of Chemoprophylaxis for Recurrent Stage I Bladder Tumors: Comparisons of Placebo, Pyridoxine, and Topical Thiotepa. In: Pavone-Macaluso, M., Smith, P.H. and Edsmyn, F., Eds., Bladder Tumors and Other Topics in Urological Oncology, Plenum, New York, 363-370.
https://doi.org/10.1007/978-1-4613-3030-1_74

has been cited by the following article:

• TITLE: Adaptive Conditional Hazard Regression Modeling of Multiple Event Times

  AUTHORS: George J. Knafl

  KEYWORDS: Adaptive Regression, Fractional Polynomials, Hazard Rate, Multiple Event Times, Recurrent Events

  JOURNAL NAME: Open Journal of Statistics, Vol.13 No.4, August 11, 2023

  ABSTRACT: Recurrent event time data and more general multiple event time data are commonly analyzed using extensions of Cox regression, or proportional hazards regression, as used with single event time data. These methods treat covariates, either time-invariant or time-varying, as having multiplicative effects while general dependence on time is left un-estimated. An adaptive approach is formulated for analyzing multiple event time data. Conditional hazard rates are modeled in terms of dependence on both time and covariates using fractional polynomials restricted so that the conditional hazard rates are positive-valued and so that excess time probability functions (generalizing survival functions for single event times) are decreasing. Maximum likelihood is used to estimate parameters adjusting for right censored event times. Likelihood cross-validation (LCV) scores are used to compare models. Adaptive searches through alternate conditional hazard rate models are controlled by LCV scores combined with tolerance parameters. These searches identify effective models for the underlying multiple event time data. Conditional hazard regression is demonstrated using data on times between tumor recurrence for bladder cancer patients. Analyses of theory-based models for these data using extensions of Cox regression provide conflicting results on effects to treatment group and the initial number of tumors. On the other hand, fractional polynomial analyses of these theory-based models provide consistent results identifying significant effects to treatment group and initial number of tumors using both model-based and robust empirical tests. Adaptive analyses further identify distinct moderation by group of the effect of tumor order and an additive effect to group after controlling for nonlinear effects to initial number of tumors and tumor order. Results of example analyses indicate that adaptive conditional hazard rate modeling can generate useful insights into multiple event time data.