Alsulaim Asma Y, Azam Faisal, Sebastian Tunny, Mahdi Hassan Fathelrahman, AbdulAzeez Sayed, Borgio J Francis, Alzahrani Faisal M
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Consultant Medical Oncologist, King Fahad specialist Hospital, Dammam, Saudi Arabia.
Saudi J Biol Sci. 2022 Jan;29(1):183-189. doi: 10.1016/j.sjbs.2021.08.073. Epub 2021 Aug 27.
Venous thromboembolism (VTE) is one of the major complications in most cancer patients leading to poor prognosis and short survival. Several common clinical risk factors coexist in cancer patients are used as risk predictive biomarkers to help in the management and prevention of VTE. These include cancer site and stage, chemotherapy regimen and elevated biological markers. However, Genetic polymorphisms in genes controlling coagulation and fibrinolysis significantly associated with VTE if detected, then they might be more sensitive individual predictive biomarkers for VTE risk assessment. This study was conducted to evaluate the association between rs3809865 and rs5918 with VTE risk as well as monitor the effect of VTE on overall survival of these cancer patients. In this retrospective case-control study, 195 cancer patients' formalin-fixed paraffin embedded tissue (FFPE) samples were collected (controls n = 157, case n = 38) using the stored data through Jan 2010 to Sep 2018 from King Fahad Specialist Hospital in Dammam. Samples were genotyped using TaqMan genotyping assay, then logistic regression analysis and Chi-square were used to predict the association between risk factors and VTE. Survival Comparison was tested by the log-rank test. Genetic polymorphisms in ITGB3 (rs3809865 and rs5918) found not to be associated with VTE increasing risk in cancer patients (>0.05). While the advanced stage was potentially increasing the risk of VTE events (OR 5.1 CI 2.01-12.9 = 0.001). Patients with VTE showed a poor overall survival reflected by the median survival rate of only three years compared to seven years for cancer patients without VTE. This study highlighted the potential influence of VTE on prognosis and survival of cancer patients and raised the importance of exploring risk predictive biomarkers in our population. This will improve the risk prediction biomarkers leading to implementing safe and effective thrombosis prophylaxis strategies.
静脉血栓栓塞症(VTE)是大多数癌症患者的主要并发症之一,会导致预后不良和生存期缩短。癌症患者中并存的几种常见临床风险因素被用作风险预测生物标志物,以帮助管理和预防VTE。这些因素包括癌症部位和分期、化疗方案以及生物标志物升高。然而,如果检测到控制凝血和纤溶的基因中的遗传多态性与VTE显著相关,那么它们可能是更敏感的个体VTE风险评估预测生物标志物。本研究旨在评估rs3809865和rs5918与VTE风险之间的关联,并监测VTE对这些癌症患者总体生存的影响。在这项回顾性病例对照研究中,利用达曼法赫德国王专科医院2010年1月至2018年9月的存储数据,收集了195例癌症患者的福尔马林固定石蜡包埋组织(FFPE)样本(对照组n = 157,病例组n = 38)。使用TaqMan基因分型检测对样本进行基因分型,然后采用逻辑回归分析和卡方检验来预测风险因素与VTE之间的关联。通过对数秩检验进行生存比较。发现ITGB3基因中的遗传多态性(rs3809865和rs5918)与癌症患者VTE风险增加无关(>0.05)。而晚期可能会增加VTE事件的风险(OR 5.1,CI 2.01 - 12.9 = 0.001)。VTE患者的总体生存情况较差,中位生存率仅为三年,而无VTE的癌症患者为七年。本研究强调了VTE对癌症患者预后和生存的潜在影响,并提高了在我们人群中探索风险预测生物标志物的重要性。这将改善风险预测生物标志物,从而实施安全有效的血栓预防策略。