Hepatocellular carcinoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients administered with either sorafenib, lenvatinib, atezolizumab plus bevacizumab, duruvalumab with/without tremelimumab, regorafenib, ramucirumab or cabozantinib for hepatocellular carcinoma at the participating institutions between May 2009 and December 2023
Exclusion criteria
Exclusion criteria: Patient without adequate baseline information due to reasons such as an initiation of treatment at another institution Patients without adequate follow-up period for reasons such as transferring to another hospital before radiological assessment of treatment response Patients considered inappropriate as subjects for this study by the principal investigator or researchers involved in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression-free survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival Best overall response Objective response rate Disease control rate Proportion of patients undergoing curative conversion therapy Treatment-related adverse events | — |
Countries
Japan
Contacts
Graduate School of Medicine, Kyoto University Department of Gastroenterology and Hepatology