Blom Jeanet W, Doggen Carine J M, Osanto Susanne, Rosendaal Frits R
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
JAMA. 2005 Feb 9;293(6):715-22. doi: 10.1001/jama.293.6.715.
Venous thrombosis is a common complication in patients with cancer, leading to additional morbidity and compromising quality of life.
To identify individuals with cancer with an increased thrombotic risk, evaluating different tumor sites, the presence of distant metastases, and carrier status of prothrombotic mutations.
DESIGN, SETTING, AND PATIENTS: A large population-based, case-control (Multiple Environmental and Genetic Assessment [MEGA] of risk factors for venous thrombosis) study of 3220 consecutive patients aged 18 to 70 years, with a first deep venous thrombosis of the leg or pulmonary embolism, between March 1, 1999, and May 31, 2002, at 6 anticoagulation clinics in the Netherlands, and separate 2131 control participants (partners of the patients) reported via a questionnaire on acquired risk factors for venous thrombosis. Three months after discontinuation of the anticoagulant therapy, all patients and controls were interviewed, a blood sample was taken, and DNA was isolated to ascertain the factor V Leiden and prothrombin 20210A mutations.
Risk of venous thrombosis.
The overall risk of venous thrombosis was increased 7-fold in patients with a malignancy (odds ratio [OR], 6.7; 95% confidence interval [CI], 5.2-8.6) vs persons without malignancy. Patients with hematological malignancies had the highest risk of venous thrombosis, adjusted for age and sex (adjusted OR, 28.0; 95% CI, 4.0-199.7), followed by lung cancer and gastrointestinal cancer. The risk of venous thrombosis was highest in the first few months after the diagnosis of malignancy (adjusted OR, 53.5; 95% CI, 8.6-334.3). Patients with cancer with distant metastases had a higher risk vs patients without distant metastases (adjusted OR, 19.8; 95% CI, 2.6-149.1). Carriers of the factor V Leiden mutation who also had cancer had a 12-fold increased risk vs individuals without cancer and factor V Leiden (adjusted OR, 12.1; 95% CI, 1.6-88.1). Similar results were indirectly calculated for the prothrombin 20210A mutation in patients with cancer.
Patients with cancer have a highly increased risk of venous thrombosis especially in the first few months after diagnosis and in the presence of distant metastases. Carriers of the factor V Leiden and prothrombin 20210A mutations appear to have an even higher risk.
静脉血栓形成是癌症患者常见的并发症,会增加发病率并降低生活质量。
识别癌症患者中血栓形成风险增加的个体,评估不同肿瘤部位、远处转移的存在情况以及血栓前突变的携带者状态。
设计、地点和患者:一项基于人群的大型病例对照研究(静脉血栓形成危险因素的多环境和基因评估[MEGA]),研究对象为1999年3月1日至2002年5月31日期间在荷兰6家抗凝诊所连续就诊的3220例年龄在18至70岁之间、首次发生腿部深静脉血栓或肺栓塞的患者,以及通过问卷调查报告静脉血栓形成后天危险因素的2131名对照参与者(患者的配偶)。在抗凝治疗停止3个月后,对所有患者和对照进行访谈,采集血样并分离DNA,以确定因子V莱顿突变和凝血酶原20210A突变。
静脉血栓形成的风险。
与无恶性肿瘤的人相比,恶性肿瘤患者静脉血栓形成的总体风险增加了7倍(比值比[OR],6.7;95%置信区间[CI],5.2 - 8.6)。血液系统恶性肿瘤患者静脉血栓形成的风险最高,经年龄和性别调整后(调整后的OR,28.0;95%CI,4.0 - 199.7),其次是肺癌和胃肠道癌。恶性肿瘤诊断后的最初几个月内静脉血栓形成的风险最高(调整后的OR,53.5;95%CI,8.6 - 334.3)。有远处转移的癌症患者比无远处转移的患者风险更高(调整后的OR,19.8;95%CI,2.6 - 149.1)。携带因子V莱顿突变且患有癌症的患者比无癌症且无因子V莱顿突变的个体风险增加了12倍(调整后的OR,12.1;95%CI,1.6 - 88.1)。对癌症患者凝血酶原20210A突变的风险也进行了间接计算,结果相似。
癌症患者静脉血栓形成的风险显著增加,尤其是在诊断后的最初几个月以及存在远处转移时。因子V莱顿和凝血酶原20210A突变的携带者似乎风险更高。