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An observational study of apatinib combined with XELOX regimen in postoperative adjuvant therapy of colorectal cancer

An observational study of apatinib combined with XELOX regimen in postoperative adjuvant therapy of colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050816
Enrollment
Unknown
Registered
2021-09-04
Start date
2021-09-03
Completion date
Unknown
Last updated
2022-05-09

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

Conditions

Colorectal cancer

Interventions

experimental group:Apatinib combined with oxaliplatin and capecitabine (XELOX) g

Sponsors

The Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years, male or female; 2. Patients with pathologically or histologically confirmed colorectal cancer; 3. High-risk stage II patients; 4. Patients with stage III; 5. Four weeks after surgery; 6. ECOG 0-2; 7. Adequate hematologic function: neutrophil absolute count >= 1.5 x 10^9/L, platelet count >= 100 x 10^9/L, hemoglobin >= 90 g/L; 8. Adequate liver function: Aspartate transferase (AST) = 50 ml/min (Cockcroft-Gault formula); 10. Adequate coagulation function: International standardized ratio (INR) or prothrombin time (PT) <= 1.5 times normal upper limit; If the patient is receiving anticoagulant therapy, INR/PT is within the prescribed anticoagulant range; 11. The subject understands and voluntarily signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Received molecular targeted drug therapy, radiotherapy and chemotherapy other than apatinib before enrollment; 3. Patients with grade II or higher myocardial ischemia or myocardial infarction and poorly controlled arrhythmias (including QTc interval >= 450 ms in males and >= 470 ms i n females); 4. Patients with active bleeding; 5. Patients with gastrointestinal ulcer, intestinal perforation or intestinal obstruction; 6. Hypertension patients with poor blood pressure control after antihypertensive drug treatment (systolic blood pressure > 160 mmHg, diastolic blood pressure > 100 mmHg); 7. Urine routine showed urine protein >= ++ or confirmed 24-hour urine protein quantification > 1.0 g; 8. Have a history of mental illness or substance abuse.

Design outcomes

Primary

MeasureTime frame
Disease free survival;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactZhou Lianbang

The Second Affiliated Hospital of Anhui Medical University

1983892355@qq.com+86 18130079699

Outcome results

None listed

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