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Clinical and translational study of targeted Vascular Endothelial growth Factor receptor combined with chemotherapy in the treatment of metastatic ascites of gastric Cancer

Clinical and translational study of targeted Vascular Endothelial growth Factor receptor combined with chemotherapy in the treatment of metastatic ascites of gastric Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017221
Enrollment
Unknown
Registered
2018-07-18
Start date
2018-01-01
Completion date
Unknown
Last updated
2018-07-23

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

Conditions

Gastric cancer

Interventions

study group:oral apatinib
study group:paclitaxel intravenous

Sponsors

First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. advanced gastric cancer or gastroesophageal junction adenocarcinoma confirmed by histopathology and/or cytology; 2. malignant ascites (positive cytology of ascites); 3. recurrent and metastatic lesions, previously received at least first-line chemotherapy; 4. Aged 18 to 75 years old; 5. ECOG 0 to 2 points; 6. Estimated survival time = 3 months; 7. Blood tests meet the following requirements: WBC = 3×10^9/L, ANC = 1.5×10^9/L, Hb=80g/L, PLT=80×10^9/L; TBIL=1.5×ULN (upper limit of normal value), ALT and AST=2×ULN (if there is liver metastasis, =5×ULN; Endogenous creatinine clearance Rate = 60 ml/min (Cockcroft-Gault formula).

Exclusion criteria

Exclusion criteria: 1. Previously used for recurrence and metastatic foci; use of taxanes or anti-angiogenic drugs; 2. gastrointestinal bleeding or active hemorrhage in other areas or patients with risk of bleeding; 3. abnormal coagulation; 4. occurred within one year before screening Arterial/venous thromboembolic events; 5. active infections (including intra-abdominal infections); 6. uncontrolled diarrhea; and 7. patients with hypertension who cannot be reduced to normal range by antihypertensive drugs (systolic blood pressure >140 mmHg/diastolic pressure) > 90 mmHg; 8. suffering from coronary heart disease, arrhythmia and cardiac insufficiency = II; 9. chronic kidney disease; 10. pregnant or lactating women, and men and women who are unwilling to adopt contraceptive measures.

Design outcomes

Primary

MeasureTime frame
paracentesis-free interval;

Secondary

MeasureTime frame
progression-free survival;overall survival;overall survival;quality of life score;

Countries

China

Contacts

Public ContactMa Tai

First Affiliated Hospital of Anhui Medical University

matayd@yeah.net+86 13956959871

Outcome results

None listed

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