Microparticles and D-dimers improve prediction of chemotherapy-associated thrombosis in cancer patients

C. Mohamed, Bennaoum Mohamed Nazim, A. Affaf, Zmouli Noujoum, Yafour Nabil, Arabi Abdessamad, Elhorri Mohamed, Badsi Dounia, Seghier Fatima
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Abstract

Background: The cancer is associated with a state of hypercoagulability, which may be the cause of venous thromboembolism (VTE), representing an undeniable cause of morbidity and mortality. Our study aimed to investigate the role of hypercoagulability markers (D-dimers, microparticles, and V Leiden mutation) in predicting cancer-associated VTE. Methods: A prospective cohort study was conducted among cancer patients who will receive chemotherapy in the Medical Oncology and Hematology departments of the EHU of Oran, Algeria from February 2013 to May 2015, followed by an observation period of two years. First, we evaluated the risk of cancer-related VTE by hypercoagulability parameters (D-dimers, microparticles, V Leiden mutation). In the second step, we tested the predictive value of the Khorana risk score (KRS) of cancer-related VTE. Then, we developed and tested the predictive value of an expanded score based on the addition of predictive biomarkers to the KRS parameters. Results: A total of 165 patients were included in our study whose median age was 62 years. More than half were males (52.7%). After an observation period of 2 years, ten patients (6.0%) developed a VTE. Among the criteria studied, only the D-dimers and the microparticles were predictive of VTE in cancer. The positive predictive value (PPV) of the KRS was 13.6%, and the negative predictive value (NPV) was 97.9%. After adding two predictive biomarkers (D-dimers and microparticles), the expanded score had a better predictive value with a PPV of 23.5% and a VPN of 98.6%. Conclusion: The addition of hypercoagulability biomarkers (microparticles and D-dimers) to the routine clinical and biological parameters of the KRS enhances the predictive potential of VTE risk in cancer.
微颗粒和d -二聚体改善癌症患者化疗相关血栓的预测
背景:这种癌症与高凝状态有关,这可能是静脉血栓栓塞(VTE)的原因,这是不可否认的发病率和死亡率的原因。我们的研究旨在探讨高凝性标志物(d -二聚体、微粒和V Leiden突变)在预测癌症相关静脉血栓栓塞中的作用。方法:对2013年2月至2015年5月在阿尔及利亚奥兰市EHU内科肿瘤科和血液科接受化疗的癌症患者进行前瞻性队列研究,观察期为2年。首先,我们通过高凝参数(d -二聚体、微粒、V Leiden突变)评估癌症相关静脉血栓栓塞的风险。在第二步,我们测试了Khorana风险评分(KRS)对癌症相关静脉血栓栓塞的预测价值。然后,我们开发并测试了基于在KRS参数中添加预测性生物标志物的扩展评分的预测值。结果:我们的研究共纳入165例患者,中位年龄为62岁。一半以上为男性(52.7%)。经过2年的观察,10例(6.0%)发生静脉血栓栓塞。在研究的标准中,只有d -二聚体和微粒能预测癌症的静脉血栓栓塞。阳性预测值(PPV)为13.6%,阴性预测值(NPV)为97.9%。在加入两种预测生物标志物(d -二聚体和微粒)后,扩展评分具有更好的预测价值,PPV为23.5%,VPN为98.6%。结论:在KRS的常规临床和生物学参数中加入高凝性生物标志物(微颗粒和d -二聚体)可增强对癌症VTE风险的预测潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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