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Observation and exploratory study on the efficacy and safety of ultrasound-guided microwave ablation combined with targeted immunotherapy for advanced liver cancer

Observation and exploratory study on the efficacy and safety of ultrasound-guided microwave ablation combined with targeted immunotherapy for advanced liver cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106643
Enrollment
Unknown
Registered
2025-07-28
Start date
2025-07-30
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Hepatocellular carcinoma

Interventions

Experimental group:MWA+Apatinib+Camrelizumab

Sponsors

Henan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years old, gender is not limited 2. Patients with primary liver cancer confirmed by histopathological or cytological examination 3. BCLC stage is B-C 4. ECOG 0-1 points 5. Child-Pugh grade A or B <=7 points 6. Tolerable surgery and no history of target-free drug allergy 7. Patients are expected to survive for more than 3 months 8. Subjects voluntarily join this study and sign the informed consent form, with good compliance.

Exclusion criteria

Exclusion criteria: 1. Diffuse liver cancer; 2. Mixed liver cancer with intrahepatic cholangiocellular carcinoma 3. Suffering from grade II. or above myocardial ischemia or myocardial infarction, poorly controlled arrhythmias (including QTc interval >=470 ms); According to NYHA standards, cardiac insufficiency grade III.~IV., or cardiac color ultrasound examination shows that the left ventricular ejection fraction (LVEF) 1.5 or prothrombin time (PT) >ULN 4 seconds or APTT >1.5 ULN), with bleeding tendency or receiving thrombolytic or anticoagulant therapy; 5. Pregnant or lactating women; Patients of childbearing potential who are unwilling or unable to take effective contraceptive measures; 6. Have a history of mental illness or psychotropic drug abuse; 7. Combined HIV-infected patients; 8. History of esophageal (fundus) variceal rupture and bleeding; 9. Other researchers think that they are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Disease control rate;Progression-free survival;Overall survival;Immune function indicators;Safety;Consistency analysis of therapeutic efficacy;

Countries

China

Contacts

Public ContactHao Zhuang/Yan Zhao

Henan Cancer Hospital

zhh8764@163.com+86 186 0373 1088

Outcome results

None listed

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