Sillah Arthur, Faria Faiza, Watson Nathaniel F, Gozal David, Phipps Amanda I
Department of Epidemiology, University of Washington School of Public Health, Seattle, Washington.
Epidemiology Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.
J Clin Sleep Med. 2020 May 15;16(5):667-673. doi: 10.5664/jcsm.8312. Epub 2020 Feb 6.
In vitro and animal studies suggest that intermittent hypoxia characterizing sleep apnea contributes to accelerated cancer progression. However, the impact of sleep apnea on survival subsequent to cancer diagnosis is unknown.
We identified a cohort of 1,575 adults diagnosed with sleep apnea between 2005 and 2014 with a subsequent cancer diagnosis via linkage of the University of Washington Medicine system and a population-based cancer registry serving the same Seattle-Puget Sound region. We computed age-standardized 5-year relative survival after cancer diagnosis for all cancers combined, and for specific cancer sites, for both the sleep apnea cohort and the general Seattle-Puget Sound population, and we used US life tables as the reference population. Relative survival was estimated by sex, cancer stage, and health care engagement.
Five-year overall relative survival for cancer was more favorable in the sleep apnea cohort than in the general population [83.6%, 95% confidence interval (CI): 79.8%-86.8% vs 71.6%, 95% CI: 71.3%-71.9%]; this pattern was applicable to most specific cancer sites. However, 5-year relative survival was slightly less favorable in the sleep apnea cohort among patients with melanoma (97.7%, 95% CI: 84.6%-99.7% vs 99.2%, 95% CI: 98.8%-99.5%) and cancer of the corpus uteri (84.0%, 95% CI: 58.2%-94.5% vs 84.6%, 95% CI: 83.1%-86.0%).
The fact that survival after cancer, overall and for most cancer sites, was more favorable in patients with sleep apnea warrants larger community-based studies to further tease out effects of sleep apnea and treatment on site-specific survival for different cancer types, particularly in patients with melanoma or uterine cancer.
体外研究和动物研究表明,睡眠呼吸暂停所特有的间歇性缺氧会促使癌症进展加速。然而,睡眠呼吸暂停对癌症诊断后生存率的影响尚不清楚。
我们通过华盛顿大学医学系统与服务于西雅图-普吉特海湾地区的基于人群的癌症登记处之间的关联,确定了一组在2005年至2014年间被诊断为睡眠呼吸暂停且随后被诊断出患有癌症的1575名成年人。我们计算了睡眠呼吸暂停队列和西雅图-普吉特海湾地区普通人群在癌症诊断后的年龄标准化5年相对生存率,所有癌症合并计算以及特定癌症部位分别计算,并将美国生命表作为参考人群。根据性别、癌症分期和医疗保健参与情况估计相对生存率。
癌症的5年总体相对生存率在睡眠呼吸暂停队列中比在普通人群中更有利[83.6%,95%置信区间(CI):79.8%-86.8% vs 71.6%,95%CI:71.3%-71.9%];这种模式适用于大多数特定癌症部位。然而,在患有黑色素瘤(97.7%,95%CI:84.6%-99.7% vs 99.2%,95%CI:98.8%-99.5%)和子宫体癌(84.0%,95%CI:58.2%-94.5% vs 84.6%,95%CI:83.1%-86.0%)的患者中,睡眠呼吸暂停队列的5年相对生存率略低。
睡眠呼吸暂停患者癌症诊断后的总体生存率以及大多数癌症部位的生存率更有利这一事实,需要开展更大规模的基于社区的研究,以进一步梳理睡眠呼吸暂停及其治疗对不同癌症类型的特定部位生存率的影响,尤其是对黑色素瘤或子宫癌患者。