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A Predictive Score for Thrombosis Associated with Breast, Colorectal, Lung, or Ovarian Cancer: The Prospective COMPASS-Cancer-Associated Thrombosis Study.与乳腺癌、结直肠癌、肺癌或卵巢癌相关的血栓形成的预测评分:前瞻性 COMPASS-癌症相关血栓形成研究。
Oncologist. 2017 Oct;22(10):1222-1231. doi: 10.1634/theoncologist.2016-0414. Epub 2017 May 26.
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Cancer-associated venous thromboembolism: Burden, mechanisms, and management.癌症相关的静脉血栓栓塞:负担、机制与管理
Thromb Haemost. 2017 Jan 26;117(2):219-230. doi: 10.1160/TH16-08-0615. Epub 2016 Nov 24.
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A systematic review of biomarkers for the prediction of thromboembolism in lung cancer - Results, practical issues and proposed strategies for future risk prediction models.肺癌中预测血栓栓塞生物标志物的系统评价——结果、实际问题及未来风险预测模型的建议策略
Thromb Res. 2016 Dec;148:63-69. doi: 10.1016/j.thromres.2016.10.020. Epub 2016 Oct 26.
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Predictors of active cancer thromboembolic outcomes: validation of the Khorana score among patients with lung cancer.活动性癌症血栓栓塞结局的预测因素:肺癌患者中Khorana评分的验证
J Thromb Haemost. 2016 Sep;14(9):1773-8. doi: 10.1111/jth.13378. Epub 2016 Sep 9.
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Epidemiology and risk factors for venous thromboembolism in lung cancer.肺癌患者静脉血栓栓塞症的流行病学及危险因素
Curr Opin Oncol. 2016 Mar;28(2):145-9. doi: 10.1097/CCO.0000000000000262.
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Venous thromboembolism prophylaxis and treatment in patients with cancer: american society of clinical oncology clinical practice guideline update 2014.癌症患者的静脉血栓栓塞预防与治疗:美国临床肿瘤学会2014年临床实践指南更新
J Clin Oncol. 2015 Feb 20;33(6):654-6. doi: 10.1200/JCO.2014.59.7351. Epub 2015 Jan 20.
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Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy.接受化疗的门诊癌症患者静脉血栓栓塞的一级预防
Cochrane Database Syst Rev. 2014 Aug 29(8):CD008500. doi: 10.1002/14651858.CD008500.pub3.
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Thromboembolism in lung cancer - an area of urgent unmet need.肺癌中的血栓栓塞——一个亟待满足的未满足需求领域。
Lung Cancer. 2014 Jun;84(3):275-80. doi: 10.1016/j.lungcan.2014.02.009. Epub 2014 Feb 28.
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Prevention and treatment of venous thromboembolism--International Consensus Statement.静脉血栓栓塞症的预防与治疗——国际共识声明
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前瞻性评估临床高凝风险因素和生物标志物,以识别有发生癌症相关性血栓风险的肺腺癌患者:观察性 ROADMAP-CAT 研究。

Prospective Assessment of Clinical Risk Factors and Biomarkers of Hypercoagulability for the Identification of Patients with Lung Adenocarcinoma at Risk for Cancer-Associated Thrombosis: The Observational ROADMAP-CAT Study.

机构信息

Oncology Unit, 3rd Dept. of Medicine, National and Kapodistrian University of Athens, School of Medicine, "Sotiria" General Hospital, Athens, Greece.

Cancer Biology and Therapeutics, Centre de Recherche Saint-Antoine, INSERM U938, Institut Universitaire de Cancérologie (IUC), Faculté de Médecine, Sorbonne Université, Paris, France.

出版信息

Oncologist. 2018 Nov;23(11):1372-1381. doi: 10.1634/theoncologist.2017-0530. Epub 2018 Aug 13.

DOI:10.1634/theoncologist.2017-0530
PMID:30104289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6291320/
Abstract

BACKGROUND

The aim of this prospective study was to identify the most clinically relevant hypercoagulability biomarkers in lung adenocarcinoma patients for elaboration of an improved risk assessment model (RAM) for venous thromboembolism (VTE).

SUBJECTS, MATERIALS, AND METHODS: One hundred fifty ambulatory patients with lung adenocarcinoma were prospectively enrolled. Thrombin generation, procoagulant phospholipid-dependent clotting time (Procoag-PPL), tissue factor activity (TFa), factor VIIa (FVIIa), factor V (FV), antithrombin, D-Dimers, P-selectin, and heparanase levels were assessed in platelet-poor plasma at inclusion (baseline) and at the end of the third chemotherapy cycle (third chemotherapy). Cox regression analysis was used to identify independent VTE predictors.

RESULTS

At baseline, patients had significantly attenuated thrombin generation, shorter Procoag-PPL, higher levels of TFa, D-Dimers, and heparanase, and lower levels of FVIIa and P-selectin, compared with controls. A significant increase in Procoag-PPL, FV, and FVIIa and a decrease of P-selectin levels were observed between baseline and third chemotherapy. Hospitalization within the last 3 months prior to assessment, time since cancer diagnosis less than 6 months, mean rate index (MRI) of thrombin generation, and Procoag-PPL were independently associated with symptomatic VTE. Accordingly, a prediction model including Procoag-PPL and MRI showed significant discriminating capacity (area under the curve: 0.84).

CONCLUSION

Ambulatory patients with lung adenocarcinoma may display pronounced blood hypercoagulability due to decreased Procoag-PPL, increased endothelial cell activation, and increased degradation of fibrin. Incorporation of Procoag-PPL and MRI of thrombin generation may improve the accuracy of a VTE-RAM in the above setting.

IMPLICATIONS FOR PRACTICE

The prospective ROADMAP-CAT study identified two biomarkers of hypercoagulability, the procoagulant phospholipid-dependent clotting time (Procoag-PPL) and the mean rate index (MRI) of the propagation phase of thrombin generation assessed with the Calibrated Automated Thrombinoscope, as being clinically relevant for the classification of ambulatory patients with lung adenocarcinoma receiving a maximum of one cycle of chemotherapy into high and intermediate/low risk for venous thromboembolism. Measurement of Procoag-PPL and MRI within 1 month after the administration of the first chemotherapy cycle provides significant accuracy of the assessment. Association of the Procoag-PPL and MRI with the clinical risk assessment model for cancer-associated thrombosis in ambulatory patients with solid tumors (COMPASS-CAT RAM) further improved its accuracy.

摘要

背景

本前瞻性研究旨在确定与肺腺癌患者相关的最具临床意义的高凝生物标志物,以完善静脉血栓栓塞症(VTE)风险评估模型(RAM)。

对象、材料和方法:前瞻性纳入 150 例门诊肺腺癌患者。在纳入时(基线)和第三次化疗周期末(第三次化疗),用血小板缺乏血浆评估凝血酶生成、促凝磷脂依赖性凝血时间(Procoag-PPL)、组织因子活性(TFa)、因子 VIIa(FVIIa)、因子 V(FV)、抗凝血酶、D-二聚体、P-选择素和肝素酶水平。采用 Cox 回归分析识别 VTE 的独立预测因子。

结果

与对照组相比,基线时患者的凝血酶生成明显减弱,Procoag-PPL 更短,TFa、D-二聚体和肝素酶水平更高,而 FVIIa 和 P-选择素水平更低。从基线到第三次化疗,Procoag-PPL、FV 和 FVIIa 显著增加,P-选择素水平显著降低。在评估前的最近 3 个月内住院、癌症诊断时间少于 6 个月、凝血酶生成的平均速率指数(MRI)和 Procoag-PPL 与症状性 VTE 独立相关。因此,包括 Procoag-PPL 和凝血酶生成 MRI 的预测模型具有显著的鉴别能力(曲线下面积:0.84)。

结论

肺腺癌门诊患者由于 Procoag-PPL 减少、内皮细胞激活增加和纤维蛋白降解增加,可能表现出明显的血液高凝状态。在这种情况下,纳入 Procoag-PPL 和凝血酶生成的 MRI 可能会提高 VTE-RAM 的准确性。

实践意义

前瞻性 ROADMAP-CAT 研究确定了两个高凝生物标志物,即促凝磷脂依赖性凝血时间(Procoag-PPL)和用 Calibrated Automated Thrombinoscope 评估的凝血酶生成扩展阶段的平均速率指数(MRI),它们对接受最多一个周期化疗的肺腺癌门诊患者的静脉血栓栓塞风险分类具有临床意义。在第一次化疗周期后 1 个月内测量 Procoag-PPL 和 MRI 可显著提高评估的准确性。Procoag-PPL 和 MRI 与用于实体瘤门诊患者的癌症相关血栓形成的临床风险评估模型(COMPASS-CAT RAM)的联合应用进一步提高了其准确性。