首页|肾细胞癌患者舒尼替尼治疗前后三维斑点追踪成像参数值变化及对心脏毒性的预警价值

肾细胞癌患者舒尼替尼治疗前后三维斑点追踪成像参数值变化及对心脏毒性的预警价值

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目的 探讨肾细胞癌患者舒尼替尼治疗前后三维斑点追踪成像(3D-STI)参数值变化及对心脏毒性的预警价值.方法 选取2020年11月至2022年3月本院收治的肾细胞癌患者226例作为观察组,随访18个月记录心脏毒性事件发生情况,选取同期体检健康者226例作为对照组.对比观察组、对照组及观察组中发生心脏毒性事件与未发生心脏毒性事件患者的3D-STI参数值[整体面积应变(GAS)、整体径向应变(GRS)、整体纵向应变(GLS)、整体圆周应变(GCS)、左心室扭转角度(LVtw)、三维左心室射血分数(3D-LVEF)、心肌综合指数(MCI)].分析肾细胞癌患者舒尼替尼辅助治疗致心脏毒性的影响因素,受试者工作特征曲线(ROC曲线)分析3D-STI参数值对心脏毒性的预警价值,限制性立方样条图分析3D-STI参数值与心脏毒性发生风险间的剂量-效应关系.结果 观察组治疗1个周期后GAS、GLS、LVtw、MCI低于治疗前,GAS、GLS、LVtw、MCI低于对照组(P<0.05);观察组226例患者随访18个月,脱落9例,有效随访217例(96.02%),发生心脏毒性事件55例(25.35%),与未发生心脏毒性患者对比,吸烟例数、饮酒例数、高血压例数、局部症状例数、IMDC评分分层、α羟丁氨酸脱氢酶水平增加,治疗1个周期后GAS、GLS、LVtw、MCI降低(P<0.05);α-羟丁氨酸脱氢酶水平增加是发生心脏毒性的独立危险因素,GAS、MCI升高是发生心脏毒性的独立保护因素(P<0.05);治疗1个周期后,GAS、MCI单独预测肾细胞癌患者舒尼替尼辅助治疗致心脏毒性的AUC值分别为0.814、0.875,联合预测的AUC值为 0.910,具有更高预测价值;GAS(x2=16.708,P<0.001)、MCI(x2=17.426,P<0.001)与心脏毒性发生风险间存在非线性剂量-反应关系,当GAS<32.73%,MCI<168.74%×°时,GAS(β=-0.709,95%CI=0.283~0.842,P<0.001)、MCI(β=-0.630,95%CI=0.356~0.811,P<0.001)与心脏毒性发生风险呈负相关.结论 肾细胞癌患者舒尼替尼治疗过程中3D-STI参数值变化与心脏毒性发生风险关系密切,且存在"阈值效应",可为临床早期预测心脏毒性发生风险提供参考.
Research on changes of parameters of three-dimensional spot tracking imaging(3D-STI)in patients with renal cell carcinoma(RCC)before and after treatment with sunitinib and its early warning value for cardiotoxicity
Objective To investigate the change of the parameters of three-dimensional spot tracking ima-ging(3D-STI)before and after the treatment with sunitinib in patients with renal cell carcinoma(RCC)and its early warning value for cardiotoxicity.Methods A total of 226 patients with RCC in the Hospital from November 2020 to March 2022 were selected as observation group,and the occurrence of cardiac tox-icity events was recorded during a follow-up period of 18 months.And 226 healthy subjects were selected as control group.The 3D-STI parameter values[global area strain(GAS),global radial strain(GRS),glob-al longitudinal strain(GLS),global circumferential strain(GCS),left ventricular twist(LVtw),3D-left ventricular ejection fraction(3D-LVEF),myocardial composite index(MCI)]were compared between the observation group,control group,and the observation group for the patients with cardiac toxicity.The in-fluencing factors of cardiotoxicity induced by sunitinib adjuvant therapy in patients with renal cell carcino-ma were analyzed.Receiver operating characteristic curve(ROC curve)was used to analyze the early warning value of 3D-STI parameters for cardiotoxicity.The dose-response relationship between 3D-STI parameters and the risk of cardiotoxicity was analyzed with restricted cubic spline plots.Results GAS,GLS,LVtw and MCI after 1 cycle of the treatment were lower than before the treatment in observation group,and GAS,GLS,LVtw and MCI in observation group after 1 cycle of the treatment were lower than those in control group(P<0.05).Among the 226 patients in the observation group,9 cases of shedding were followed up for 18 months,217 cases(96.02%)were effectively followed up,and 55 cases(25.35%)had cardiotoxic events.Compared with the patients without cardiotoxicity,the number of smoking cases,drinking cases,hypertension cases,local symptoms cases,IMDC score delamination,a-hydroxybutyrate dehydrogenase levels were increased,and GAS,GLS,LVtw and MCI was decreased after 1 cycle of the treatment(P<0.05).The increase in α-hydroxybutyrate dehydrogenase levels was an independent risk factor for cardiac toxicity,while the elevation of GAS and MCI was an independent protective factor for cardiac toxicity(P<0.05).After 1 cycle of the treatment,the AUC value of GAS and MCI alone in pre-dicting cardiotoxicity induced by sunitinib adjuvant therapy in patients with renal cell carcinoma was 0.814 and 0.875,respectively,and theAUC value of combined prediction was 0.910,and it had higher predictive value.There was a nonlinear dose-response relationship between GAS(x2=16.708,P<0.001),MCI(x2=17.426,P<0.001)and the risk of cardiotoxicity.When GAS<32.73%,MCI<168.74%×°,GAS(β=-0.709,95%CI=0.283~0.842,P<0.001),MCI(β=-0.630,95%CI=0.356~0.811,P<0.001)were negatively correlated with the risk of cardiotoxicity.Conclusion The change of 3D-STI pa-rameters during sunitinib is closely related to the risk of cardiotoxicity in patients with renal cell carcino-ma,and there is a"threshold effect",which can provide a reference for predicting the risk of cardiotoxicity in early clinical stage.

renal cell carcinomasunitinibcardiotoxicitythree-dimensional spot tracking imaging(3D-STI)

方慧杰、张鑫、翟玉翠、史丽娟、田国祥

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中国人民解放军总医院第七医学中心老年医学科,北京 100700

中国人民解放军总医院第七医学中心肾脏病科,北京 100700

肾细胞癌 舒尼替尼 心脏毒性 三维斑点追踪成像(3D-STI)

北京市科技计划项目

KJ2022CX731

2024

新疆医科大学学报
新疆医科大学

新疆医科大学学报

CSTPCD
影响因子:0.76
ISSN:1009-5551
年,卷(期):2024.47(6)