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A study for neoadjuvant radiotherapy combined with surgery in the treatment of hepatocellular carcinoma with microvascular invasion

A study for neoadjuvant radiotherapy combined with surgery in the treatment of hepatocellular carcinoma with microvascular invasion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017663
Enrollment
Unknown
Registered
2018-08-08
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

hepatocellular carcinoma

Interventions

Group 1:Neoadjuvant radiotherapy before operation
Group 2:Non intervention before operation

Sponsors

The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female or male aged 18 years and over, but no more than 70 years; 2. Histologic or cytologic confirmation of advanced hepatocellular carcinoma; 3. CT imaging findings with microvascular invasion; 4. Single lesion,4cm<diameter=6cm; 5. ECOG=0-2, Child-pugh A-B; 6. Liver reserve function ICGR15<20%; 7. Patients had not received systemic venous chemotherapy ever before; 8. Be able to receive surgery; 9. Provision of informed consent; 10. Be able to follow the research program and follow up process.

Exclusion criteria

Exclusion criteria: 1. radiotherapy and chemotherapy with experimental drug within 3 months before the start of study therapy; 2. Have at least another primary malignant tumor; 3. Active infection with bacterial or fungal infection; 4. Patients with HIV infection, HCV infection, serious coronary artery disease or asthma, serious cerebrovascular disease or other diseases that the researchers think can not be entered into the group; 5. Women who are pregnant or breast feeding; 6. Drug abuse, clinical or psychological or social factors which will influence the informed. consent or the study implementation; 7. History of hepatectomy 8. influence the safety or compliance of the patients.

Design outcomes

Primary

MeasureTime frame
OS;PFS;Safety;Local recurrence;Intrahepatic metastases;

Secondary

MeasureTime frame
Tumor marker;Routine blood test;liver function;

Countries

China

Contacts

Public ContactXu Qingxiang

The Affiliated Hospital of Nanjing University Medical School

xqx008dg@sina.com+86 13915967870

Outcome results

None listed

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