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Efficacy and safety of drug-eluting microspheres combined with anti-angiogenic drugs in the treatment of colorectal liver metastases who have failed second-line chemotherapy in China

Efficacy and safety of drug-eluting microspheres combined with anti-angiogenic drugs in the treatment of colorectal liver metastases who have failed second-line chemotherapy in China

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045317
Enrollment
Unknown
Registered
2021-04-12
Start date
2021-07-01
Completion date
Unknown
Last updated
2021-11-22

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

Conditions

colorectal liver metastases

Interventions

D-TACE group:D-TACE+Regorafenib

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with colorectal liver metastases,and have clear pathology; 2.No obstructive jaundice; No large vessel invasion; Meet the indications for interventional chemoembolization; 3.Voluntary taking anti-angiogenic drugs as a third-line treatment, Willing to accept interventional treatment; 4.The patient voluntarily participated in the study and signed an informed consent form; 5.18-80 years old; no gender limit; 6.Evaluable lesions according to RECIST standards.

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 using other chemotherapy drugs and targeted drugs; 4.Patients with severe 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.Those who are contraindicated in the use of anti-angiogenic drugs and drug-eluting microspheres.

Design outcomes

Primary

MeasureTime frame
Overall Survival;

Secondary

MeasureTime frame
Time-to-Disease Progression;Objective Response Rate;

Countries

China

Contacts

Public ContactZhou Bo

Zhongshan Hospital, Fudan University

bonheurzhou@hotmail.com+86 18616880602

Outcome results

None listed

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