Multivariate Bayesian meta-analysis: joint modelling of multiple cancer types using summary statistics

被引:4
|
作者
Jahan, Farzana [1 ]
Duncan, Earl W. [1 ]
Cramb, Susana M. [2 ]
Baade, Peter D. [3 ]
Mengersen, Kerrie L. [1 ]
机构
[1] Queensland Univ Technol, Sch Math Sci, Fac Sci & Engn, ARC Ctr Excellence Math & Stat Frontiers, Brisbane, Qld 4001, Australia
[2] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[3] Canc Council Queensland, 553 Gregory Terrace, Brisbane, Qld 4006, Australia
基金
澳大利亚研究理事会;
关键词
Cancer incidence; Cancer atlas; Online estimates; BREAST-CANCER; LUNG-CANCER; COLORECTAL-CANCER; PROGNOSTIC-FACTOR; DISEASE; ASSOCIATION; PATTERNS; SMOKING;
D O I
10.1186/s12942-020-00234-0
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Cancer atlases often provide estimates of cancer incidence, mortality or survival across small areas of a region or country. A recent example of a cancer atlas is the Australian cancer atlas (ACA), that provides interactive maps to visualise spatially smoothed estimates of cancer incidence and survival for 20 different cancer types over 2148 small areas across Australia. Methods The present study proposes a multivariate Bayesian meta-analysis model, which can model multiple cancers jointly using summary measures without requiring access to the unit record data. This new approach is illustrated by modelling the publicly available spatially smoothed standardised incidence ratios for multiple cancers in the ACA divided into three groups: common, rare/less common and smoking-related. The multivariate Bayesian meta-analysis models are fitted to each group in order to explore any possible association between the cancers in three remoteness regions: major cities, regional and remote areas across Australia. The correlation between the pairs of cancers included in each multivariate model for a group was examined by computing the posterior correlation matrix for each cancer group in each region. The posterior correlation matrices in different remoteness regions were compared using Jennrich's test of equality of correlation matrices (Jennrich in J Am Stat Assoc. 1970;65(330):904-12. 10.1080/01621459.1970.10481133). Results Substantive correlation was observed among some cancer types. There was evidence that the magnitude of this correlation varied according to remoteness of a region. For example, there has been significant negative correlation between prostate and lung cancer in major cities, but zero correlation found in regional and remote areas for the same pair of cancer types. High risk areas for specific combinations of cancer types were identified and visualised from the proposed model. Conclusions Publicly available spatially smoothed disease estimates can be used to explore additional research questions by modelling multiple cancer types jointly. These proposed multivariate meta-analysis models could be useful when unit record data are unavailable because of privacy and confidentiality requirements.
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页数:19
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