Centre for Public Health, Queen's University Belfast, Belfast, UK.
Belfast Health and Social Care Trust, Belfast, UK.
Aliment Pharmacol Ther. 2018 Jan;47(2):279-288. doi: 10.1111/apt.14388. Epub 2017 Nov 3.
Angiotensin receptor blockers (ARBs; including candesartan, losartan, olmesartan and valsartan) are widely used to treat hypertension, heart failure and diabetic neuropathy. There is considerable pre-clinical evidence that ARBs can reduce cancer progression, particularly for gastric cancer. Despite this, epidemiological studies have yet to assess the impact of ARB use on gastro-oesophageal cancer survival.
To investigate the association between post-diagnosis ARB use and gastro-oesophageal cancer survival.
We selected a cohort of patients with newly-diagnosed gastro-oesophageal cancer between 1998 and 2012 from English cancer registries. We linked to prescription and clinical records from the Clinical Practice Research Datalink, and to death records from the Office for National Statistics. We used time-dependant Cox-regression models to calculate hazard ratios (HRs) comparing gastro-oesophageal cancer-specific mortality between post-diagnosis ARB users and non-users, after adjusting for demographics, comorbidities and post-diagnosis aspirin or statin use.
Our cohort included 5124 gastro-oesophageal cancer patients, of which 360 used ARBs, and 3345 died due to their gastro-oesophageal cancer during follow-up. After adjustment, ARB users had moderately lower risk of gastro-oesophageal cancer mortality than the non-users (HR = 0.83, 95% CI 0.71-0.98). There was evidence of a dose-response relationship with the lowest HRs observed among patients receiving at least 2 years of prescriptions (HR = 0.42, 95% CI 0.25-0.72).
In this large population-based gastro-oesophageal cancer cohort, we found moderately reduced cancer-specific mortality among ARB users. However, confirmation in further independent epidemiological studies with sufficient staging information is required.
血管紧张素受体阻滞剂(ARB;包括坎地沙坦、氯沙坦、奥美沙坦和缬沙坦)广泛用于治疗高血压、心力衰竭和糖尿病性神经病。有大量临床前证据表明 ARB 可以降低癌症的进展速度,特别是胃癌。尽管如此,流行病学研究尚未评估 ARB 使用对胃食管癌症生存的影响。
调查诊断后 ARB 使用与胃食管癌症生存之间的关系。
我们从英国癌症登记处选择了一组 1998 年至 2012 年间新诊断为胃食管癌症的患者。我们与临床实践研究数据链接中的处方和临床记录以及国家统计局的死亡记录进行了链接。我们使用时间依赖性 Cox 回归模型来计算诊断后 ARB 使用者与非使用者之间胃食管癌症特异性死亡率的风险比(HR),并在调整了人口统计学、合并症和诊断后阿司匹林或他汀类药物使用情况后进行比较。
我们的队列包括 5124 名胃食管癌症患者,其中 360 名患者使用了 ARB,3345 名患者在随访期间因胃食管癌症而死亡。调整后,ARB 使用者的胃食管癌症死亡率风险略低于非使用者(HR = 0.83,95%CI 0.71-0.98)。存在剂量反应关系,接受至少 2 年处方的患者的最低 HR 观察到(HR = 0.42,95%CI 0.25-0.72)。
在这项大型基于人群的胃食管癌症队列研究中,我们发现 ARB 使用者的癌症特异性死亡率适度降低。然而,需要进一步的独立流行病学研究来确认,这些研究应具有足够的分期信息。