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Apatinib in the treatment for advanced Hepatocellular Carcinoma: a prospective, multi-center study

Apatinib in the treatment for advanced Hepatocellular Carcinoma: a prospective, multicenter study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024269
Enrollment
Unknown
Registered
2019-07-04
Start date
2019-07-15
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

hepatocellular carcinoma

Interventions

Sponsors

Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years, male and female (calculated on the date of signing the informed consent); 2. Hepatocellular carcinoma patients diagnosed by histopathology and/or cytology: 1)Not suitable for surgery and / or local treatment; 2)Progress after surgical and/or topical treatment. 3. Liver function Child-Pugh score <= 7 points; 4. ECOG PS 0-1; 5. BCLC staging: B/C; 6. Plan to use apatinib monotherapy or apatinib in combination with other treatments; 7. Voluntary participation in the study, signing informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Exclude patients with contraindications to anti-angiogenic drugs: 1) The patient has hypertension and cannot be controlled by antihypertensive medication; 2) Urine routinely shows protein positive >= ++; 3) A variety of factors affecting oral medications (unable to swallow, chronic diarrhea, intestinal obstruction, etc.); 4) abnormal blood coagulation, bleeding tendency: for example, active ulcers, fecal occult blood (++), etc.; 5) Grade 3-4 cardiac insufficiency (NYHA standard); 6) Severe hepatorenal insufficiency (grade 4); 3. According to the investigator's judgment, there are serious concomitant diseases that endanger the safety of the patient or affect the patient's completion of the study; 4. The estimated survival time is less than 3 months.

Design outcomes

Primary

MeasureTime frame
Progress Free Survival;

Secondary

MeasureTime frame
Overall survival;Objective response rate;Time to tumor progression;Disease control rate;Quality of Life Score;

Countries

China

Contacts

Public ContactErlei Zhang

Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology

baiyu19861104@163.com+86 13419507667

Outcome results

None listed

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