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A preliminary clinical study of acatinib mesylate combined with docetaxel and fluorouracil in the treatment of advanced gastric cancer or gastro esophageal junction adenocarcinoma.

A preliminary clinical study of acatinib mesylate combined with docetaxel and fluorouracil in the treatment of advanced gastric cancer or gastro esophageal junction adenocarcinoma.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015577
Enrollment
Unknown
Registered
2018-04-09
Start date
2018-04-09
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

gastric cancer or gastro esophageal junction adenocarcinoma

Interventions

Case series:apatinib

Sponsors

Nongken Hostipal, Heilongjiang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years male and female; 2. Advanced gastric cancer or gastro esophageal junction adenocarcinoma patients confirmed by pathologically and previously unaccepted drug treatment; 3. ECOG 0-2;4.Estimated survival time=3 mouths; 4. Estimated survival time=3 mouths; 5. Confirmed by pathology with measurable lesions, (CT scan Long diameter of tumor=10mm, CT scan Long diameter of lymph node lesion=15mm, scan slice thickness>5mm); 6. The main organ function is normal, and meet the following standards: (1)The standard of blood routine examination should be consistent: HB=90 g/L, ANC=1.5×10^9/L, PLT=80×10^9/L (2) Biochemical tests should meet the following criteria: BIL45ml/min. 7. Fertile woman must perform a pregnancy test (serum or urine) 7 days before screened, or voluntarily adopt proper methods of contraception during the observation period and 8 week after the last given apatinib; 8. Patients voluntarily entered the study and signed informed consent form (ICF).

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. High blood pressure and failure to be reduced to normal range by antihypertensive drugs(Systolic pressure > 140 mmHg, diastolic pressure >90mmHg); 3. Variety of factors affecting oral drugs (such as inability to swallow, chronic diarrhea, and intestinal obstruction); 4. Coagulopathy (INR>1.5×ULN APTT>1.5×ULN), with Bleeding tendency; 5. Urinary protein is more than + + and confirmed the 24 hour urinary protein quantitative>1g; 6. Received apatinib or other VEGFR inhibitors, such as bevacizumab, Solafinib, Sunitinib; 7. Metastases of the central nervous system with symptoms; 8. Other cases the researchers judged that could affect the outcome of the clinical study.

Design outcomes

Primary

MeasureTime frame
PFS;

Countries

China

Contacts

Public ContactGao Feng
834287905@qq.com+86 13936552301

Outcome results

None listed

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