Department of Cardiology & Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Center for Cardiovascular Research (DZHK), Partner Site Berlin, Charité-Universitätsmedizin Berlin (Campus CVK), Berlin, Germany.
Department of Cardiology, Charité Universitätsmedizin Berlin (Campus CBF), Berlin, Germany.
Eur J Heart Fail. 2020 Jul;22(7):1230-1238. doi: 10.1002/ejhf.1782. Epub 2020 Mar 23.
Cancer patients suffer from impaired cardiovascular function. Elevated resting heart rate (RHR) has been identified as a marker for increased long-term mortality in cancer patients prior to the receipt of anticancer treatment. We aimed to establish whether RHR is associated with survival in treatment-naïve cancer patients.
This prospective study enrolled 548 unselected treatment-naïve cancer patients between 2011 and 2013. The median age of the cohort was 62 years; 40.9% were male and 32.7% had metastatic disease. Median RHR was 72 b.p.m. Most patients were in sinus rhythm (n = 507, 92.5%). Clinical heart failure was noted in 37 (6.8%) patients. RHR was not related to cancer stage (P = 0.504). Patients in the highest RHR tertile had higher levels of high-sensitivity troponin (P = 0.003) and N-terminal pro-B-type natriuretic peptide (P = 0.039). During a median follow-up of 25 months (interquartile range: 16-32 months; range: 0-40 months), 185 (33.8%) patients died from any cause [1-year-mortality: 17%, 95% confidence interval (CI) 13-20%]. In univariate survival analysis, RHR predicted all-cause mortality [crude hazard ratio (HR) for a 5 b.p.m. increase in RHR: 1.09, 95% CI 1.04-1.15; P < 0.001], and remained significantly associated with outcome after adjustment for age, gender, tumour entity, tumour stage, cardiac status and haemoglobin (adjusted HR for a 5 b.p.m. increase in RHR: 1.10, 95% CI 1.04-1.16; P < 0.001). There was no significant impact of metastatic/non-metastatic disease state on the predictive value of RHR (P = 0.433 for interaction). In subgroup analyses, the strongest associations for RHR with mortality were observed in lung (crude HR 1.14; P = 0.007) and gastrointestinal (crude HR 1.31; P < 0.001) cancer.
Treatment-naïve cancer patients with higher RHRs display higher levels of cardiovascular biomarkers. RHR was independently associated with all-cause mortality, especially in lung and gastrointestinal cancers. Elevated RHR and cardiovascular biomarkers may represent early signs of incipient cardiac dysfunction.
癌症患者的心血管功能受损。在接受抗癌治疗之前,静息心率(RHR)升高已被确定为癌症患者长期死亡率增加的标志物。我们旨在确定 RHR 是否与未经治疗的癌症患者的生存率相关。
本前瞻性研究纳入了 2011 年至 2013 年间的 548 名未经选择的未经治疗的癌症患者。队列的中位年龄为 62 岁;40.9%为男性,32.7%患有转移性疾病。中位 RHR 为 72 b.p.m. 大多数患者处于窦性节律(n=507,92.5%)。37 例(6.8%)患者出现临床心力衰竭。RHR 与癌症分期无关(P=0.504)。RHR 最高三分位组的高敏肌钙蛋白(P=0.003)和 N 末端 pro-B 型利钠肽(P=0.039)水平更高。在中位随访 25 个月(四分位间距:16-32 个月;范围:0-40 个月)期间,185 名(33.8%)患者因任何原因死亡[1 年死亡率:17%,95%置信区间(CI)为 13-20%]。在单变量生存分析中,RHR 预测全因死亡率[RHR 每增加 5 b.p.m.的粗危险比(HR):1.09,95%CI 为 1.04-1.15;P<0.001],并且在调整年龄、性别、肿瘤实体、肿瘤分期、心脏状况和血红蛋白后,与结果仍显著相关(RHR 每增加 5 b.p.m.的调整 HR:1.10,95%CI 为 1.04-1.16;P<0.001)。转移性/非转移性疾病状态对 RHR 预测价值无显著影响(交互作用 P=0.433)。在亚组分析中,RHR 与死亡率的最强关联见于肺癌(粗 HR 1.14;P=0.007)和胃肠道癌(粗 HR 1.31;P<0.001)。
静息心率较高的未经治疗的癌症患者显示出更高水平的心血管生物标志物。RHR 与全因死亡率独立相关,尤其是在肺癌和胃肠道癌中。升高的 RHR 和心血管生物标志物可能代表早期心脏功能障碍的迹象。