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A real-world study for apatinib mesylate as adjuvant therapy for patients at high risk of recurrence of hepatocellular carcinoma after surgery

A real-world study for apatinib mesylate as adjuvant therapy for patients at high risk of recurrence of hepatocellular carcinoma after surgery

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029799
Enrollment
Unknown
Registered
2020-02-14
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-02-17

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

Conditions

HCC

Interventions

Case series:Apatinib

Sponsors

General Hospital of the People's Liberation Army of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old both male and female; 2. Patients with hepatocellular carcinoma after surgical resection or local ablation (PEI or percutaneous puncture or intraoperative RFA); 3. Postoperative pathology suggested that there was no residual on the cutting edge, and CR was confirmed by imaging within 3 to 7 weeks after surgery; 4. Preoperative imaging (CT/MRI/ pet-ct, etc.), intraoperative or postoperative pathology and other examinations suggested at least one high-risk factor for recurrence: Group 1: the number of tumors >=3; Group 2: differentiation degree for III or IV level (the Edmondson - Steiner level 4 (I - IV) classification method). Group 3: hepatic vein, portal vein, bile duct or inferior vena cava can be seen under the gross or microscopic view and can be surgically removed, except for single tumor with diameter =200ng/ml), and remained >=200 ng/ml 1 to 2 months after surgery. Group 5: tumor rupture; Group 6: there was no clear fibrous capsule or incomplete capsule between the tumor and liver tissue; Group 7: satellite nodules were found on the excised specimen; Group 8: tumor in special location (e.g. adjacent to left, middle, right or inferior vena cava); 5. Voluntarily join the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Proven allergic to apatinib mesylate tablets and/or their excipients; 2. Pregnant or nursing women; 3. Patients with apatinib contraindications; 4. The doctor thinks not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
effectiveness;

Countries

China

Contacts

Public ContactKaishan Tao

The First Hospital Affiliated to The Fourth Military Medical University

taokaishan0686@163.com+86 13909250686

Outcome results

None listed

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