Department of Population Health, University of Kansas Medical Center (KUMC), University of Kansas Cancer Center, Kansas City, KS, USA.
Department of Anesthesiology, University of Kansas Medical Center (KUMC), University of Kansas Cancer Center, KS, USA.
J Natl Cancer Inst. 2021 Apr 6;113(4):425-433. doi: 10.1093/jnci/djaa122.
Despite high rates of opioid therapy, evidence about the risk of preventable opioid harms among cancer survivors is underdeveloped. Our objective was to estimate the odds of opioid use disorder (OUD) and overdose following breast, colorectal, or prostate cancer diagnosis among Medicare beneficiaries.
We conducted a retrospective cohort study using 2007-2014 Surveillance, Epidemiology, and End Results-Medicare data for cancer survivors with a first cancer diagnosis of stage 0-III breast, colorectal, or prostate cancer at age 66-89 years between 2008 and 2013. Cancer survivors were matched to up to 2 noncancer controls on age, sex, and Surveillance, Epidemiology, and End Results region. Using Firth logistic regression, we estimated adjusted 1-year odds of OUD or nonfatal opioid overdose associated with a cancer diagnosis. We also estimated adjusted odds of OUD and overdose separately and by cancer stage, prior opioid use, and follow-up time.
Among 69 889 cancer survivors and 125 007 controls, the unadjusted rates of OUD or nonfatal overdose were 25.2, 27.1, 38.9, and 12.4 events per 10 000 patients in the noncancer, breast, colorectal, and prostate samples, respectively. There was no association between cancer and OUD. Colorectal survivors had 2.3 times higher odds of opioid overdose compared with matched controls (adjusted odds ratio = 2.33, 95% confidence interval = 1.49 to 3.67). Additionally, overdose risk was greater in those with more advanced disease, no prior opioid use, and preexisting mental health conditions.
Opioid overdose was a rare, but statistically significant, outcome following stage II-III colorectal cancer diagnosis, particularly among previously opioid-naïve patients. These patients may require heightened screening and intervention to prevent inadvertent adverse opioid harms.
尽管阿片类药物治疗率很高,但癌症幸存者可预防的阿片类药物危害的证据仍不充分。我们的目的是估计在医疗保险受益人群中,乳腺癌、结直肠癌或前列腺癌诊断后发生阿片类药物使用障碍(OUD)和过量用药的几率。
我们使用 2007-2014 年监测、流行病学和最终结果-医疗保险数据进行了一项回顾性队列研究,纳入了在 2008 年至 2013 年间年龄在 66-89 岁、患有 0-III 期乳腺癌、结直肠癌或前列腺癌的癌症幸存者。对癌症幸存者按年龄、性别和监测、流行病学和最终结果区域与最多 2 名非癌症对照者进行匹配。我们使用费希尔逻辑回归估计了癌症诊断后 OUD 或非致命性阿片类药物过量的 1 年调整后几率。我们还分别按癌症分期、既往阿片类药物使用情况和随访时间调整了 OUD 和过量的几率。
在 69889 名癌症幸存者和 125007 名对照者中,非癌症、乳腺癌、结直肠癌和前列腺样本中 OUD 或非致命性过量的未经调整发生率分别为 25.2、27.1、38.9 和 12.4 例/10000 例患者。癌症与 OUD 无关。与匹配的对照组相比,结直肠癌幸存者发生阿片类药物过量的几率高 2.3 倍(调整后的优势比=2.33,95%置信区间:1.49-3.67)。此外,疾病分期更晚、无既往阿片类药物使用史和存在精神健康状况的患者,其过量风险更高。
在 II-III 期结直肠癌诊断后,阿片类药物过量是一种罕见但具有统计学意义的结局,特别是在以前未曾使用过阿片类药物的患者中。这些患者可能需要加强筛查和干预,以防止意外的阿片类药物不良后果。