Skip to content

Multicenter clinical study on the efficacy and safety of drug-eluting microspheres combined with anti-angiogenic drugs in Chinese patients with colon cancer liver metastases who failed second-line chemotherapy

Multicenter clinical study on the efficacy and safety of drug-eluting microspheres combined with anti-angiogenic drugs in Chinese patients with colon cancer liver metastases who failed second-line chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055497
Enrollment
Unknown
Registered
2022-01-11
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

colorectal cancer liver metastases

Interventions

Group 1:D-TACE + Regorafenib
Group 2:Oral antiangiogenic drugs

Sponsors

Zhongshan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with liver metastases from colorectal cancer with clear pathology; 2. No obstructive jaundice; 3. Voluntary use of anti-angiogenic drugs as third-line therapy; 4. Patients voluntarily participate in the study and sign the informed consent; 5. Aged over 18 years, and less than 80 years; gender is not limited; 6. There are evaluable lesions according to RECIST criteria.

Exclusion criteria

Exclusion criteria: 1. Patients who cannot be followed up as required by the study; 2. Patients without independent decision-making ability or mental illness; 3. Patients who are being treated with other chemotherapy drugs and targeted drugs; 4. Patients with serious heart, brain, liver and kidney system diseases; 5. The expected survival time is less than 3 months; 6. Those who are allergic or intolerant to the use of anti-angiogenic drugs and drug-eluting microspheres; 7. The use of anti-angiogenic drugs and drug-eluting microspheres is contraindicated.

Design outcomes

Primary

MeasureTime frame
Overall Survival;

Secondary

MeasureTime frame
Progression Free Survival;Objective Response Rate;Disease Control Rate;

Countries

China

Contacts

Public ContactZhou Bo

Zhongshan Hospital Affiliated to Fudan University

bonheurzhou@hotmail.com+86 18616880602

Outcome results

None listed

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