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Retrospective real-world study on the efficacy and safety of bevacizumab combined with chemotherapy/radiotherapy/immunization in the treatment of metastatic colorectal cancer

Retrospective real-world study on the efficacy and safety of bevacizumab combined with chemotherapy/radiotherapy/immunization in the treatment of metastatic colorectal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400085101
Enrollment
Unknown
Registered
2024-05-30
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

Metastatic colorectal cancer

Interventions

Treatment Group:None

Sponsors

Danyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Visit from January 1st, 2023 to December 31st, 2023; 2) Age = 18 years old; 3) Patients with metastatic colorectal cancer confirmed by histology or cytology; 4) Indications for the use of bevacizumab according to clinical diagnosis and treatment conventions; 5) ECOG score 0-1 points; 6) Accept a treatment regimen containing bevacizumab in combination with chemotherapy, radiation therapy, immunization, etc.

Exclusion criteria

Exclusion criteria: 1) Patients with concomitant malignant tumors; 2) Individuals who are allergic to bevacizumab and its excipients; 3) Individuals with severe damage to the liver, kidneys, hematopoiesis, and cardiovascular system; 4) Pregnant or lactating women; 5) Patients with previous gastrointestinal perforation and fistula, including gallbladder perforation; Those who have undergone major surgery within 4 weeks before administration or whose wounds have not fully healed within 4 weeks before administration; 6) Patients with tumor infiltration into large blood vessels or proximal tracheal and bronchial networks, or recent occurrence of pulmonary hemorrhage/hemoptysis (>1/2 teaspoon of fresh red blood), or other risks of major bleeding; 7) Researchers believe that other conditions that are not suitable for treatment, such as active tuberculosis, cardiovascular accidents, cerebrovascular accidents, drug use, alcoholism, and other bad habits.

Design outcomes

Primary

MeasureTime frame
Progression free survival;Objective relief rate;Describe the number and proportion of users of bevacizumab combined with chemotherapy/radiotherapy/immunization;

Secondary

MeasureTime frame
Adverse reaction incidence rate;Types and severity of adverse reactions;

Countries

China

Contacts

Public ContactLifang DING

Danyang People's Hospital

dinglifang1979@163.com+86 138 6246 8906

Outcome results

None listed

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