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Clinical Trials/NCT01047618
NCT01047618
Completed
Not Applicable

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

Asan Medical Center1 site in 1 country259 target enrollmentDecember 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advanced Gastric Cancer
Sponsor
Asan Medical Center
Enrollment
259
Locations
1
Primary Endpoint
To evaluate the incidence of VTE in advanced gastric cancer with chemotherapy and to identify risk factors and biomarkers for VTE in this population
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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.

Detailed Description

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

Registry
clinicaltrials.gov
Start Date
December 2009
End Date
December 2014
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yoon-Koo Kang

Professor

Asan Medical Center

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

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

Time Frame: 2 years

Secondary Outcomes

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

Study Sites (1)

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