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A prospective, open and nonrandomised cohort study on the prevention of recurrence of cancer by using Amlotinb after radical hepatectomy for hepatocellular carcinoma

A prospective, open and nonrandomised cohort study on the prevention of recurrence of cancer by using Amlotinb after radical hepatectomy for hepatocellular carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017921
Enrollment
Unknown
Registered
2018-08-22
Start date
2018-09-30
Completion date
Unknown
Last updated
2018-09-17

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

Conditions

Hepatocellular Cancer

Interventions

Group 1:Anlotinib, TACE after hepatectomy 1 month later
Group 2:TACE treatment after hepatectomy 1 month later

Sponsors

Shanghai Public Health Clinical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed liver cancer patients, 18-80 years old, liver function Child A grade, ECOG score 0-1 points; 2. No gross vascular or cholangiocarcinoma, no extrahepatic metastasis, postoperative pathology confirmed poor differentiation and / or MVI in hepatocellular carcinoma; 3. The tumor RO is completely removed.

Exclusion criteria

Exclusion criteria: 1. Patients who have been treated or relapsed with liver cancer, younger than 18 years old or older than 80 years old; 2. Liver function Child B grade and above, creatinine higher than the upper limit of normal, eGFR less than 90, ECOG score of 2 or more, cardiopulmonary function and other clear surgical contraindications; 3. There is no effective control of hypertension, postoperative incision healing is not good, surgical wounds are caused by biliary or infection due to effusion and drainage can not be removed; 4. The tumor can not be removed by RO, there are macroscopic blood vessels or cholangiocarcinoma, there is extrahepatic metastasis; 5. Postoperative pathology confirmed high differentiation of hepatocellular carcinoma or non-hepatocellular carcinoma.

Design outcomes

Primary

MeasureTime frame
AFP;

Secondary

MeasureTime frame
Liver Function;Crea;eGFR;

Countries

China

Contacts

Public ContactHuang Yangqing

Shanghai Public Health Clinical Center

eric_huangyq@163.com+86 18121150837

Outcome results

None listed

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