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A Clinical study on the establishment of treatment protocol for huge hepatocellular carcinoma based on individualized prognosis prediction

A Clinical study on the establishment of treatment protocol for huge hepatocellular carcinoma based on individualized prognosis prediction

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036873
Enrollment
Unknown
Registered
2020-08-25
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-21

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

Conditions

huge hepatocellular carcinoma

Interventions

Transcatheter arterial chemoembolization (TACE) plus Sorafenib Group:ranscatheter arterial chemoembolization (TACE) plus Sorafenib

Sponsors

Shanghai Eastern Hepatobiliary Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. voluntarily participates in the group with good compliance; cooperates with experimental observation and signs a written informed consent form; 2. with KPS score of the general condition >=60; 3. Aged 18 to 70 years; 4. no history of other malignant tumors; 5. no history of preoperative anti-tumor therapy; 6. WBC count > 3000/L; absolute neutrophil count > 1500/L; platelet count > 50000/L; creatinine 45%; 7. liver function of Child-Pugh class A, without cirrhosis or with mild cirrhosis, without ascites, without hepatic encephalopathy; 8. without gross tumor thrombus of portal/hepatic vein; 9. without distant metastasis; 10. adequate predicted postoperative liver volume; 11. without contraindications for surgery, TACE and sorafenib.

Exclusion criteria

Exclusion criteria: 1. pregnant and lactating women; 2. subjects with poor general condition and obvious impairment of liver function (bilirubin > 3 times the upper limit of normal value, serum albumin < 30g/L); 3. subjects with severe heart, kidney and blood diseases; 4. subjects with poor compliance; 5. subjects who have a history of allergy to chemotherapy drugs, allergic constitution or are in an allergic state; 6. subjects with treatment-related contraindications; 7. subjects with predicted survival of < 5 months.

Design outcomes

Primary

MeasureTime frame
Overall Survival;Overall Survival;

Secondary

MeasureTime frame
progression-free survival;

Countries

China

Contacts

Public ContactXia Yong

Shanghai Eastern Hepatobiliary Hospital

xiayong@smmu.edu.cn+86 13601807601

Outcome results

None listed

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