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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00735566
Other study ID # NCCCTS 04-105
Secondary ID
Status Completed
Phase N/A
First received August 13, 2008
Last updated October 16, 2012
Start date April 2006
Est. completion date January 2012

Study information

Verified date October 2012
Source National Cancer Center, Korea
Contact n/a
Is FDA regulated No
Health authority South Korea: Korea Food and Drug Administration (KFDA)
Study type Observational

Clinical Trial Summary

Endogenous antiangiogenic factors are related with gastric cancer progression.


Description:

Gastric cancers have been known to secrete the proangiogenic cytokine VEGF in vitro and in vivo. Tumor VEGF expression is correlated with the severity of disease in patients with gastric cancer and some authors have suggested using circulating VEGF as a prognostic factor or tumor marker.In addition to producing proangiogenic cytokines, recent data demonstrate that tumors can produce antiangiogenic cytokine as well. It has been suggested that, in humans, the generation of antiangiogenic compounds in the presence of a primary tumor suppresses the growth of distant metastases. This phenomenon has been demonstrated in mice and in patients with clear cell renal cancer, breast cancer, and colorectal cancer. However, the presence of endogenous antiangiogenic cytokines in patients with gastric cancer has not been reported.


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date January 2012
Est. primary completion date July 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Histologic diagnosis of gastric adenocarcinoma

- No other forms of cancer therapy, such as chemotherapy or radiotherapy for at least 3 weeks before the enrollment in study

- Performance status of 0, 1, 2 on the ECOG criteria

- ASA class I, II

- Patient compliance that allow adequate follow up

- Informed consent from patient or patient's relative.

Exclusion Criteria:

- Second primary malignancy

- EMR (Endoscopic mucosal resection) indication

- Laparoscopic gastrectomy

- Radiologic or clinical evidence of metastasis

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of National Cancer Center Goyang-si Geonggi-do

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Center, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relationship between antiangiogenic factor and tumor, node, metastasis One year No
Secondary Overall survival, treatment failure 5 years No
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