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免疫检查点抑制剂治疗患者的治疗前高敏肌钙蛋白 T 与短期心脏结局预测。

Pre-treatment high-sensitivity troponin T for the short-term prediction of cardiac outcomes in patients on immune checkpoint inhibitors.

机构信息

Cardiology Division, Pisa University Hospital, Pisa, Italy.

Institute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.

出版信息

Eur J Clin Invest. 2021 Apr;51(4):e13400. doi: 10.1111/eci.13400. Epub 2020 Sep 27.

DOI:10.1111/eci.13400
PMID:32894777
Abstract

BACKGROUND

Immune checkpoint inhibitors (ICIs) are an emerging option for several advanced metastatic cancers, but may have cardiotoxic effects. The prognostic value of high-sensitivity troponin T (hs-TnT) before treatment start has never been investigated.

MATERIALS AND METHODS

Thirty consecutive patients underwent measurement of hs-TnT before starting ICI therapy (pembrolizumab, 23%; nivolumab, 12%; atezolizumab, 6%; durvalumab, 5%). The primary endpoint of cardiovascular death, stroke or transient ischaemic attack, pulmonary embolism and new-onset heart failure, and the secondary endpoint of progression of cardiac involvement according to the CARDIOTOX classification were evaluated after 3 months from the first cycle.

RESULTS

Patients (median age 68 years, 77% men, 13% with coronary artery disease, 90% current or former smokers, 67% overweight or obese and 43% hypertensive) had a median hs-TnT of 12 ng/L (interquartile interval 8-23). The primary endpoint occurred only in patients with hs-TnT ≥ 14 ng/L at baseline. Therefore, only patients who had hs-TnT ≥ 14 ng/L before the first cycle died had a stroke/TIA or new-onset HF. Furthermore, nine out of 13 patients with the secondary endpoint (progression of cardiac disease) had hs-TnT ≥ 14 ng/L before the first cycle (P = .012). AUC values were 0.909 for the primary endpoint and 0.757 for the secondary endpoint. The best cut-off was 14 ng/L for both the primary (100% sensitivity, 73% specificity) and secondary endpoints (sensitivity 75%, specificity 77%).

CONCLUSIONS

In patients on ICIs, baseline hs-TnT predicts a composite cardiovascular endpoint and the progression of cardiac involvement at 3 months, with 14 ng/L as the best cut-off.

摘要

背景

免疫检查点抑制剂(ICIs)是几种晚期转移性癌症的新兴选择,但可能具有心脏毒性作用。在开始治疗前,高敏肌钙蛋白 T(hs-TnT)的预后价值从未被研究过。

材料和方法

连续 30 例患者在开始 ICI 治疗(帕博利珠单抗,23%;纳武利尤单抗,12%;阿替利珠单抗,6%;度伐利尤单抗,5%)前测量 hs-TnT。在第一个周期后 3 个月评估心血管死亡、中风或短暂性脑缺血发作、肺栓塞和新发心力衰竭的主要终点,以及根据 CARDIOTOX 分类评估心脏受累进展的次要终点。

结果

患者(中位年龄 68 岁,77%为男性,13%有冠状动脉疾病,90%为当前或既往吸烟者,67%超重或肥胖,43%患有高血压)的 hs-TnT 中位数为 12ng/L(四分位距 8-23)。主要终点仅发生在基线 hs-TnT≥14ng/L 的患者中。因此,只有在第一个周期前 hs-TnT≥14ng/L 的患者才会发生中风/TIA 或新发心力衰竭。此外,有 9/13 例次要终点(心脏疾病进展)患者在第一个周期前 hs-TnT≥14ng/L(P=0.012)。主要终点和次要终点的 AUC 值分别为 0.909 和 0.757。最佳截断值为 14ng/L,用于主要终点(100%敏感性,73%特异性)和次要终点(敏感性 75%,特异性 77%)。

结论

在接受 ICI 治疗的患者中,基线 hs-TnT 可预测 3 个月时的心血管复合终点和心脏受累进展,以 14ng/L 为最佳截断值。

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