Trials / Unknown
UnknownNCT05967429
Predictors of Sorafenib Response in HCC
Predictors of Sorafenib Response in Patients With Advanced Hepatocellular Carcinoma
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 80 (estimated)
- Sponsor
- Sohag University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- —
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | The neutrophil-to- lymphocyte ratio | It was calculated by dividing the neutrophil count by the lymphocyte count. |
| DIAGNOSTIC_TEST | Prognostic nutrition index | It was calculated using the following formula: serum albumin (g/L) + 0.005 × total lymphocyte count/μL |
Timeline
- Start date
- 2023-08-01
- Primary completion
- 2024-04-01
- Completion
- 2024-06-01
- First posted
- 2023-08-01
- Last updated
- 2023-08-01
Source: ClinicalTrials.gov record NCT05967429. Inclusion in this directory is not an endorsement.