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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03875417
Other study ID # HEP001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date October 31, 2018

Study information

Verified date March 2019
Source Azienda Policlinico Umberto I
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Aim of this study is to evaluate whether treating HCC recurrences in resected elderly patients is advantageous or not.


Description:

Introduction- Hepatocellular carcinoma (HCC) is the most common primary liver malignancy. It usually develops in cirrhotic liver with high recurrence rates. More than 2/3 of patients are elderly, often excluded from surgery and follow-up protocols. Aim of this study is to evaluate whether treating HCC recurrences in resected elderly patients is advantageous or not.

Materials and methods- 126 patients, aged between 65 and 90 years, submitted to liver resection for HCC were enrolled. They were divided into three classes. Class 1 included patients submitted to major resections, Class 2 to minor resections and Class 3 to minor resections associated with thermoablation. All of them were clinically and radiologically followed up. Patients who developed recurrences (Group A) were referred to further treatments (surgery, interventional radiology or pharmacological therapy). Mortality, disease-free survival (DFS), overall survival (OS) and quality of life (QoL) were evaluated and compared with non-recurrent patients (Group B).

Used interventional radiology means were Radiofrequency ablation (RF), microwaves ablation (MWA) or transcatheter arterial chemoembolization (TACE).


Recruitment information / eligibility

Status Completed
Enrollment 126
Est. completion date October 31, 2018
Est. primary completion date May 30, 2018
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- HCC patient

- eligible for surgery

Exclusion Criteria:

- non eligible for surgery at first HCC diagnosis

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
liver resection
resection of one or more HCC nodules within the liver
Thermic ablation
ablation of HCC nodule through a percutaneous needle, by using radiofrequency or microwaves
Transcatheter arterial chemoembolization
embolization of HCC nodule via drug-eluted microbeads.

Locations

Country Name City State
Italy Department of Surgery "Pietro Valdoni" Roma

Sponsors (1)

Lead Sponsor Collaborator
Azienda Policlinico Umberto I

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival survival in months follow up time 1-16 years
Primary Disease free survival survival without recurrences in months follow up time 1-16 years
Secondary Karnofsky performance scale evaluation of performance status in dimensionless scale 0 - 100 follow up time 1-16 years
Secondary Activity of Daily living assess the ability to manage common routine activities evaluated in dimensionless scale 1-6 follow up time 1-16 years
Secondary Instrumental Activity of Daily living assess the ability to use common instruments evaluated in dimensionless scale 1-8 follow up time 1-16 years
Secondary Blood Haemoglobin evaluation of mean haemoglobin levels in g/dl follow up time 1-16 years
Secondary serum Albumin evaluation of mean albumin levels in g/dl follow up time 1-16 years
Secondary Geriatric Depression Scale evaluation of depression in patients in dimensionless scale 0 - 15 follow up time 1-16 years
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