Advances in statistical methods for cancer surveillance research: an age-period-cohort perspective

Front Oncol. 2024 Feb 9:13:1332429. doi: 10.3389/fonc.2023.1332429. eCollection 2023.

Abstract

Background: Analysis of Lexis diagrams (population-based cancer incidence and mortality rates indexed by age group and calendar period) requires specialized statistical methods. However, existing methods have limitations that can now be overcome using new approaches.

Methods: We assembled a "toolbox" of novel methods to identify trends and patterns by age group, calendar period, and birth cohort. We evaluated operating characteristics across 152 cancer incidence Lexis diagrams compiled from United States (US) Surveillance, Epidemiology and End Results Program data for 21 leading cancers in men and women in four race and ethnicity groups (the "cancer incidence panel").

Results: Nonparametric singular values adaptive kernel filtration (SIFT) decreased the estimated root mean squared error by 90% across the cancer incidence panel. A novel method for semi-parametric age-period-cohort analysis (SAGE) provided optimally smoothed estimates of age-period-cohort (APC) estimable functions and stabilized estimates of lack-of-fit (LOF). SAGE identified statistically significant birth cohort effects across the entire cancer panel; LOF had little impact. As illustrated for colon cancer, newly developed methods for comparative age-period-cohort analysis can elucidate cancer heterogeneity that would otherwise be difficult or impossible to discern using standard methods.

Conclusions: Cancer surveillance researchers can now identify fine-scale temporal signals with unprecedented accuracy and elucidate cancer heterogeneity with unprecedented specificity. Birth cohort effects are ubiquitous modulators of cancer incidence in the US. The novel methods described here can advance cancer surveillance research.

Keywords: Lexis diagram; SEER program; age-period-cohort model; cancer surveillance research; statistical methods.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. PR and AM-F are supported by the Intramural Research Program of the National Cancer Institute, Division of Cancer Epidemiology and Genetics. AM-F is also supported through an appointment to the National Cancer Institute (NCI) ORISE Research Participation Program under DOE contract number DE-SC0014664.