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临床试验/NCT01047618
NCT01047618已完成不适用

The Incidence and Risk Factors of Venous Thromboembolism in Advanced Gastric Cancer Patients: Prospective Observational Study

Asan Medical Center1 个研究点 分布在 1 个国家目标入组 259 人开始时间: 2009年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
259
试验地点
1
主要终点
To evaluate the incidence of VTE in advanced gastric cancer with chemotherapy and to identify risk factors and biomarkers for VTE in this population

研究概览

简要总结

Venous thromboembolism (VTE), which includes pulmonary embolism (PE) and deep vein thrombosis (DVT), is a common complication and leading cause of death in cancer patients. Large, population-based studies have shown that patients with cancer have four- to seven-fold increased risk of developing VTE compared with patients without cancer. VTE would be frequent in patients with advanced gastric cancer, especially associated chemotherapy. However, relatively few studies have been conducted regarding the incidence of VTE in Asian cancer patients. According to previous review, Asian patients significantly lower risk of developing VTE. The rate of VTE with advanced gastric cancer, and associated chemotherapy is not known in Asian patients. In addition, the impact of VTE on overall survival has not been documented in these patients.

详细描述

Primary objectives - To evaluate the incidence of VTE in advanced gastric cancer with chemotherapy and to identify risk factors and biomarkers for VTE in this population

Secondary objectives

  • To investigate the significant impact of VTE on overall survival and in this population

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically documented gastric adenocarcinoma including adenocarcinoma of the gastro-esophageal junction
  • Age 18 years or older
  • Locally advanced (inoperable) or metastatic gastric cancer, initially diagnosed, recurrent gastric cancer
  • Performance status (ECOG scale) : 0-2
  • Adequate bone marrow function:
  • Adequate renal function
  • Adequate hepatic function:
  • Required to be at the start of a new chemotherapy regimen
  • Received chemotherapy one cycle or more
  • Adequate follow-up for at least 12 weeks
  • Patients should sign a written informed consent before study entry

排除标准

  • Previously exposed to chemotherapy exception adjuvant or neoadjuvant therapy
  • Second primary malignancy (except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin or prior malignancy treated more than 5 years ago without recurrence
  • Prior radiotherapy was administered to target lesions selected for this study, or radiotherapy to the non-target lesions has been completed within 4 weeks before randomization
  • Presence of CNS metastasis
  • Major surgery within 4 weeks before initiation of study treatment or lack of complete recovery from the effects of major surgery. Patient received curative operation or RFA for metastatic disease.
  • Significant traumatic injury within 4 weeks prior to enrollment
  • Serious illness or medical conditions, as follows:
  • Congestive heart failure (NYHA class III or IV)
  • Unstable angina or myocardial infarction within the past 12 months
  • Significant arrhythmia requiring medication and conduction abnormality such as over 2nd degree AV block
  • Uncontrolled hypertension
  • Liver cirrhosis (≥ Child class B)
  • Psychiatric disorder that may interfere with protocol compliance
  • Unstable diabetes mellitus
  • Active infection
  • Superficial thrombophlebitis, transient ischemic attacks, and thrombosis occurring in setting of disseminated intravascular coagulation
  • Pregnant or lactating women
  • Hormonal replacement therapy within 4 weeks
  • Chronic oral treatment with corticosteroid unless initiated > 6 months prior to study entry and at low dose (≤ 20mg methylprednisolone or equivalent)
  • Warfarin of heparin therapy
  • Not able or willing to give informed consent
  • Any patients judged by the investigator to be unfit to participate in the study

结局指标

主要结局

To evaluate the incidence of VTE in advanced gastric cancer with chemotherapy and to identify risk factors and biomarkers for VTE in this population

时间窗: 2 years

次要结局

  • To investigate the significant impact of VTE on overall survival and in this population(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yoon-Koo Kang

Professor

Asan Medical Center

研究点 (1)

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