IMPORTANCE Regional variation in opioid use may be attenuated when pharmaceuticalsponsored trials include care that is often standardized by protocols. Understanding such variation is important for global trials that sometimes include time to opioid use as an end point. OBJECTIVE To identify whether regional and country-level variation in opioid use exists among prostate cancer clinical trials across the world. DESIGN, SETTING, AND PARTICIPANTS International phase 3 randomized clinical trials with patients with metastatic prostate cancer and initiation from January 1, 2008, or later were identified through internal databases of the US Food and Drug Administration. Data of patients in the intention-to-treat population from each trial were pooled. Descriptive and regression analyses of the collected data were conducted from September 2018 to February 2019. EXPOSURES Cancer therapy. MAIN OUTCOMES AND MEASURES Opioid use data were from concomitant medications reported in the database for each trial. Logistic regression models, descriptive statistics, and χ2 tests were used to compare opioid use across world regions while adjusting for patient age, presence of visceral disease, bony disease, and baseline Eastern Cooperative Oncology Group Performance Status score and pain score. RESULTS In total, 9670 patients (mean [SD] age of 69.2 [8.3] years) from 8 prostate cancer clinical trials in 46 countries were included. Patients in Eastern Europe (adjusted odds ratio [AOR], 0.19; 95% CI, 0.16-0.22) and Asia (AOR, 0.31; 95% CI, 0.25-0.38) were less likely to use opioids compared with patients in North America. These findings held even when the analysis was restricted to patients who reported moderate to high pain levels at baseline (Eastern Europe: AOR, 0.16 [95% CI, 0.12-0.22]; Asia: AOR, 0.47 [95% CI, 0.29-0.79]). Within North America, rates of opioid use were similar between the United States and Canada (AOR, 1.13; 95% CI, 0.93-1.37). CONCLUSIONS AND RELEVANCE This study found that, despite the clinical trial setting, opioid use appeared to vary by world regions, suggesting that this variability should be considered in international clinical trials.
History
Publication title
JAMA Oncology
Volume
5
Issue
11
Article number
e192971
Number
e192971
ISSN
2374-2445
Department/School
Menzies Institute for Medical Research
Publisher
American Medical Association
Place of publication
United States
Rights statement
Copyright 2019 American Medical Association
Repository Status
Restricted
Socio-economic Objectives
Evaluation of health and support services not elsewhere classified