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The clinical value of dynamic monitoring of serum VEGF in evaluating the effect of advanced gastric cancer

The clinical value of dynamic monitoring of serum VEGF in evaluating the effect of advanced gastric cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052196
Enrollment
Unknown
Registered
2021-10-22
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced gastric cancer

Interventions

Case series:No

Sponsors

Yuebei People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Gastric cancer patients aged 18 to 75 years; 2. Patients with HER-2 negative advanced metastatic gastric cancer diagnosed by pathology and receiving first-line chemotherapy; 3. No obvious active bleeding. 4. Patients with an expected survival period of >= 6 months; 5. The function of major organs is normal, that is, the following standards are met: the blood routine examination standards must be met (no blood transfusion and blood products within 14 days, no correction with G-CSF and other hematopoietic stimulating factors) 6. ECOG PS score 0-1 points 7. The subjects voluntarily joined the study, signed the informed consent form, had good compliance, and cooperated with the follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with hypertension that cannot be reduced to the normal range after antihypertensive drug treatment (systolic blood pressure>140 mmHg, diastolic blood pressure>90 mmHg); 2. Severe cardiovascular disease in the past: myocardial ischemia or myocardial infarction above grade II, and poorly controlled arrhythmia (including QTc interval >=450 ms for men and >=470 ms for women); according to NYHA criteria, grades III to IV Cardiac insufficiency , or those with left ventricular ejection fraction (LVEF) less than 50% indicated by echocardiography; 3. Patients with positive urine protein (urinary protein test 2+ or above, or 24-hour urine protein quantitative> 1.0g), those with weak positive (±) proteinuria should be carefully enrolled; 4. Abnormal coagulation function (INR>1.5, APTT>1.5 ULN), with bleeding tendency; 5. Patients with a history of psychotropic drug abuse and unable to quit or patients with mental disorders; 6. Patients who have been treated with other anti-angiogenic targeted drugs in the past; 7. According to the judgment of the investigator, patients with other concomitant diseases that seriously endanger the patient's safety or affect the patient's completion of the study; 8. Those with uncontrolled central nervous system transfer; 9. Pregnant or lactating women; 10. The researcher believes that it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Peripheral serum vascular endothelial growth factor level;Progression-free survival;

Secondary

MeasureTime frame
overall survival;

Countries

China

Contacts

Public ContactZhang Guoping

Yuebei People's Hospital

zgpybyy@163.com+86 13826306668

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026