intrahepatic cholangiocarcinoma
Conditions
Interventions
None listed
Sponsors
Kyoto University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: S (study type), randomized controlled trials (RCTs), and observational studies. Studies were included if they met the following criteria: the study design was an RCT or observational study, the study discussed the OS, and the study population included patients with ICC who underwent liver resection in the presence or absence of LND.
Exclusion criteria
Exclusion criteria: Case reports, case series, and non-English-language studies were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome was the overall survival. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes were the disease-free survival, in-hospital mortality, in-hospital morbidity, operative time, blood loss during surgery, need for blood transfusion, presence of tumor cells at the resection margins, and length of hospital stay. | — |
Countries
Japan,Asia(except Japan),North America,Europe
Contacts
Public ContactTakamichi Ishii
Graduate School of Medicine, Kyoto University Department of Surgery
Outcome results
None listed