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Resection combined with ablation and stereotactic radiotherapy for colorectal cancer liver metastasis: A single-arm, prospective, real-world study

Resection combined with ablation and stereotactic radiotherapy for colorectal cancer liver metastasis: A single-arm, prospective, real-world study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059148
Enrollment
Unknown
Registered
2022-04-26
Start date
2022-04-18
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

colorectal cancer liver metastasis

Interventions

Experimental group:Resection combined with ablation and stereotactic radiotherapy

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Histologically confirmed liver metastases of colorectal cancer were evaluated as technically unresectable after systemic intravenous chemotherapy or hepatic arterial infusion chemotherapy. 2. According to RECIST V1.1, there was at least one measurable lesion in the liver. 3. The number of liver metastases should be at least 3; No unresectable extrahepatic metastases (except lung metastases). 4. Focal diameter =40% of total liver volume, and there is open flow out of liver and into liver. 5. Primary colorectal cancer is evaluated and radical resection is expected. 6. Aged 18-80 years. 7. ECOG physical state score 0 or 1. 8. With full organ and bone marrow function. 9. Expected survival >=12 weeks. 10. Sign a written informed consent and be able to comply with the visit and related procedures stipulated in the program.

Exclusion criteria

Exclusion criteria: 1. Previous history of hepatectomy or ablation (except preoperative radiofrequency ablation performed as planned). 2. Patients with arteriovenous thromboembolism events within the past 6 months who were assessed as unsuitable for surgery. 3. Diagnosis of other malignancies within 5 years prior to treatment. 4. Those who are unwilling or unable to use acceptable methods of contraception throughout the treatment period. 5. Other factors led the researchers to consider it inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Recurrence free survival;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactXing Baocai

Beijing Cancer Hospital

xingbaocai88@sina.com+86 10 88196558

Outcome results

None listed

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