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Consolidative Radiotherapy for Colorectal Cancer Liver Metastases Receiving Surgery or Radiofrequency Abation

Consolidative Radiotherapy for Colorectal Cancer Liver Metastases Receiving Surgery or Radiofrequency Abation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010999
Enrollment
Unknown
Registered
2017-03-28
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

colorectal cancer

Interventions

two:SBRT

Sponsors

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Biopsy proven unresectable mCRC (Stage IV); (2) Primary resection of CRC; (3) 1 to 3 liver metastases with an individual maximum diameter of up to 5 cm; (4) Absence of evidence of extra-hepatic disease; (5) Metastatic liver lesions reveiving R0 or R1 resection or radiofrequency ablation; (6) Presence of tumor bed; (7) ECOG PS 0-1; (8) Aged 18-70 years; (9) Patients should have adequate bone marrow function as defined by peripheral granulocyte count of =1500/mm3; (10) AST, ALT & Alkaline phosphates must be = 2.5X the upper limit of normal. Total bilirubin must be within the limit of normal; (11) Patients must provide verbal and written informed consent to participate in the study; (12) Absence of any severe pulmonary or cardiac diseases.

Exclusion criteria

Exclusion criteria: (1) Patients with either untreated brain metastases or brain metastases treated within the past three months are ineligible; (2) Patients who are pregnant; (3) Patients with severe organ dysfunction; (4) History of abdominal radiotherapy; (5) Unwillingness to participate or inability to comply with the protocol for the duration of the study; (6) Participation in any investigational drug study within 3 months preceding the start of study treatment; (7) Patients not suitable to take part in clinical trials judged by researches.

Design outcomes

Primary

MeasureTime frame
DFS;

Secondary

MeasureTime frame
intrahepatic DFS;OS;

Countries

China

Contacts

Public ContactTao Zhang

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

taozhangwh@aliyun.com+86 18971656660

Outcome results

None listed

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