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A clinical study of radiation therapy combined with TACE in liver cancer patients with portal vein tumor thrombosis

A study of percutaneous hepatic artery chemotherapy embolization (TACE) combined with radiotherapy (RT) in patients with hepatocellular carcinoma combined with portal vein tumor embolization in a different order of choice

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033573
Enrollment
Unknown
Registered
2020-06-06
Start date
2016-08-01
Completion date
Unknown
Last updated
2020-06-08

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

Conditions

Hepatocellular carcinoma, combined portal vein tumor thrombosis

Interventions

TACE+RT:TACE followed by radiotherapy
RT+TACE:RT followed by TACE

Sponsors

Third Affiliated Hospital of the Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Patients with combined portal carcinoma thrombosis of the liver assessed as unresectable by the same medical group; 3. Preoperative liver function Child A or B, thrombinogen time (PT) less than 4 seconds for normal controls. Gastroscopic esophageal veins without severe varicose, inactive gastrointestinal ulcers. No hepatic encephalopathy or/and significant ascites. Kidney function and cardiopulmonary function are basically normal. Hemoglobin >=90g/L, white blood cell count >=3.0x10^9/L, neutrophil count >=1.5x10^9/L, platelet count >=60x10^9/L; 4. Life expectancy greater than three months, no pregnancy, no HCV, HIV or syphilis infection, able to understand the circumstances of the study and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Those who have received chemotherapy, TACE, radiation therapy, targeted drugs, biological therapy, or participated in clinical trials of other drugs or instruments prior to admission to the group; 2) The tumor has developed distant metastases, e.g., lung, brain, bone, etc.; 3) Severe varicose veins of the esophagogastric floor with a tendency to bleed from the gastrointestinal tract or a previous history of haemorrhage from the gastrointestinal tract; (4) Those who, in the opinion of the investigator, are otherwise inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Overall Survival;Progression-free survival;

Countries

China

Contacts

Public ContactCheng Shuqun

Third Affiliated Hospital of the Second Military Medical University

chengshuq@aliyun.com+86 13901746139

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026