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The Overall Survival of Patients With Unresectable HCC in Real-life

The Overall Survival of Patients Diagnosed With Unresectable Hepatocellular Carcinoma Under Real-life Clinical Practice in Asia Pacific Region

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03612726
Enrollment
5000
Registered
2018-08-02
Start date
2018-07-16
Completion date
2025-12-31
Last updated
2025-03-24

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

Conditions

Hepatocellular Carcinoma

Brief summary

Liver cancer is the fifth most common cancer and the second most frequent cause of cancer-related death globally. Hepatocellular carcinoma represents about 90% of primary liver cancers and constitutes a major global health problem. The pattern of HCC occurrence shows a significant geographical imbalance, with the highest incidence rates in East Asia (more than 50% of the cases occurring in China). The aim of this study is to investigate the overall survival (OS) of patients diagnosed with unresectable hepatocellular carcinoma under real-world practice conditions in Asia Pacific region.

Interventions

None listed

Sponsors

Tokyo University
CollaboratorOTHER
Humanity & Health Medical Group Limited
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with a diagnosis of unresectable hepatocellular carcinoma * Able to comprehend and provide written informed consent in accordance with institutional guidelines.

Exclusion criteria

* Patients not willing to participate and/or give their written informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalUp to 5 yearsOverall survival (OS) is defined as the time (days) from the date of unresectable HCC diagnosis to the date of death, due to any reason. Patients alive or lost to follow-up at the time of analysis will be censored at their last date of follow-up

Secondary

MeasureTime frameDescription
Progression-free survival (PFS)Up to 5 yearsProgression-free survival (PFS) is defined as the time (days) from the start of treatment to the date of first observed disease progression (radiological or clinical, whichever is earlier) or death due to any cause, if death occurs before progression is documented
Time to progression (TTP)Up to 5 yearsTime to progression (TTP) is defined as the time (days) from the start of treatment to the first documented disease progression
Duration of treatmentUp to 5 yearsDuration of treatment, defined by the time interval from the start of treatment to the day of permanent discontinuation of treatment (including death)
Frequency and Severity of Adverse EventsUp to 5 yearsSafety will be evaluated by monitoring and recording the grade 3, 4 and 5 adverse events (AE) occurring during and after treatment throughout follow up of patients.

Countries

China, Hong Kong, Japan

Contacts

Primary ContactDanny Wang, PhD
danny.wang@hnhmgl.com+852-21160598

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026