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Predictors of Sorafenib Response in HCC

Predictors of Sorafenib Response in Patients With Advanced Hepatocellular Carcinoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05967429
Enrollment
80
Registered
2023-08-01
Start date
2023-08-31
Completion date
2024-06-30
Last updated
2023-08-01

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

Conditions

Hepatocellular Carcinoma

Keywords

Nutrition assessment, HCC, Sorafenib

Brief summary

Evaluating the nutrition status of patients with advanced HCC who received sorafenib. Using the pretreatment nutrition status and quality of life as predictors to sorafenib response

Detailed description

This a cross sectional study will be conducted on 100 HCC treated with sorafenib Data were gathered from medical records, including age sex body weight and height (BMI) pre-therapy laboratory counts of white cells, neutrophils, lymphocytes, monocyte, hemoglobin and platelets; bilirubin, albumin and globulin concentration, AST, ALT, AFP, PT and CONC Barcelona Clinic Liver Cancer Stage (BCLC) of all patients The neutrophil-to- lymphocyte ratio (NLR) was calculated by dividing the neutrophil count by the lymphocyte count. The platelet- to-lymphocyte ratio (PLR) was calculated by dividing the platelet count by the lymphocyte count. Weight loss difference after treatment Portal hypertension was defined as presence of either collaterals on radiological examination, esophageal varices by upper gastrointestinal endoscopy and/or thrombocytopenia. Quality of life assessment. QoL was assessed using FACT Hepatobiliary Symptom Index (FHSI-8) Questionnaire. QoL was assessed at base line and 3-6 months after start of treatment.

Interventions

DIAGNOSTIC_TESTThe neutrophil-to- lymphocyte ratio

It was calculated by dividing the neutrophil count by the lymphocyte count.

DIAGNOSTIC_TESTPrognostic nutrition index

It was calculated using the following formula: serum albumin (g/L) + 0.005 × total lymphocyte count/μL

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* HCC recieved sorafenib

Exclusion criteria

* Patient refuse to participate * Patients recieving other treatment modalities

Design outcomes

Primary

MeasureTime frameDescription
assessment of nutrition statusAugest 2023 to March 2024Prognostic nutrition index
Predictors of sorafenib responseAugest 2023 to March 2024The neutrophil-to- lymphocyte ratio
Assess the quality of lifeAugest 2023 to March 2024using FACT Hepatobiliary Symptom Index

Contacts

Primary ContactMona Abdelrahmam, MD
monamohamed@med.sohag.edu.eg01021025895

Outcome results

None listed

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