Anlotinib for Hepatocellular Carcinoma
AFHC
A Real World Study on the Effect of Single or Combined Treatment of Anlotinib on Survival and Prognosis of Advanced Hepatocellular Carcinoma
1 other identifier
observational
200
1 country
1
Brief Summary
The purpose of this study is to observe and explore the effect of single or combined treatment of arotinib on the survival and prognosis of patients with advanced liver cancer in the real world, and to summarize the treatment experience of a wide range of people.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2021
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 17, 2021
CompletedStudy Start
First participant enrolled
June 30, 2021
CompletedFirst Posted
Study publicly available on registry
July 8, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 5, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
July 5, 2024
CompletedJuly 8, 2021
June 1, 2021
2 years
June 17, 2021
June 29, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
OS
Overall Survival
From date of admission until the date of death from any cause, assessed up to 24 months
Secondary Outcomes (1)
PFS
From date of admission until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months
Interventions
This is an observational study
Eligibility Criteria
Patients with advanced liver cancer
You may qualify if:
- Age: ≥ 18 years old, male or female;
- Patients with advanced liver cancer were diagnosed;
- Patients assessed by doctors to benefit from single or combined treatment of arotinib;
- Patients volunteered to join the project.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
People's Hospital of Guangxi Zhuang Autonomous Region
Nanning, Guangxi, 530000, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief physician
Study Record Dates
First Submitted
June 17, 2021
First Posted
July 8, 2021
Study Start
June 30, 2021
Primary Completion
July 5, 2023
Study Completion
July 5, 2024
Last Updated
July 8, 2021
Record last verified: 2021-06
Data Sharing
- IPD Sharing
- Will not share