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Evaluation of the efficacy and safety of arsenic trioxide for the prevention of recurrence and metastasis after palliative resection of primary liver cancer under the MDT diagnosis and treatment model

Evaluation of the efficacy and safety of arsenic trioxide for the prevention of recurrence and metastasis after palliative resection of primary liver cancer under the MDT diagnosis and treatment model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17014000
Enrollment
Unknown
Registered
2017-12-17
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

primary liver cancer

Interventions

experimental group:arsenic trioxide
control group:common theray

Sponsors

Union Hospital, Tongji Medical College, Huazhong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18~70 years old; 2. The diagnosis of primary hepatocellular carcinoma (HCC); 3. Complete resection of HCC; 4. Child - Pugh A, B (less than 7) level (only two indicators of albumin and bilirubin Child - Pugh rating in one of 2); 5. The KPS score is more than 50; 6. The tumor was exposed; 7. A combined resection of a satellite or a focal point; 8. Vascular or bile duct embolus under the microscope; 9. Expentance of survival period is more than 6 months; 10. Normal heart and kidney function.

Exclusion criteria

Exclusion criteria: 1. Pregnancy and lactation period; 2. Complication of other tumors or active liver cancer; 3. Extensive metastasis has occurred in the whole body; 4. The liver function severer than the Child-Pugh C grade; 5. The blood platelet count was less than 100 x 10^9, which could not be corrected. 6. Uncontrolled medical or acute infection; 7. With disease of the nervous system, brain or meningeal metastasis; 8. Other clinical trials of similar drugs have been involved in the last 2 months; 9. Allergy to arsenic and related compounds; 10. Other systemic antitumor drugs were accepted within 3 months; 11. Chemotherapy can not be completed because of severe side effects; 12. The patient is unable to understand the purpose of the study or disagree with the requirements of the study.

Design outcomes

Secondary

MeasureTime frame
Overall survival;one year survival;

Primary

MeasureTime frame
Progression free survival;three year survival;three year survival;safety and tolerance;

Countries

China

Contacts

Public ContactJun Xiong

Union Hospital, Tongji Medical College, Huazhong University

oldxiong@188.com+86 13995536848

Outcome results

None listed

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