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Completed

NCT Number: NCT04562428

The Safety and Efficacy Evaluation of XSLJZ in Advanced Hepatocellular Carcinoma Patients With Multiple Protein Kinase Inhibitor Therapy: A Randomized, Double-Blind, Controlled Trial

The purpose of the study was search the safety and efficacy of the of Xiang Sha Liu Jun Zi Decoction (XSLJZ) in advanced hepatocellular carcinoma patients with multiple protein kinase inhibitor therapy. Evaluate the treatment effect on the symptoms of appetite and quality of life in advanced hepatocellular carcinoma patients

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Key information

Age range

20 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

China Medical University hospital

Taichung, 西屯區, 407, Taiwan

About this study

Hepatocellular carcinoma (HCC) is the top fourth most common cancer in Taiwan. Approximately 85% of cases of HCC patients had chronic HBV or HCV infection in Taiwan. Metabolic risk factors, such as obesity, fatty liver, high lipidemia, and diabetes mellitus are associated with increased risk for nonviral hepatocellular carcinoma.

The first and second-line systemic therapy approved in advanced hepatocellular carcinoma are multikinase inhubitors .Sorafenib (Nexavar)、Regorafenib and Lenvatinib are significantly improve survival in patients who had unresectable advanced and/or metastatic HCC not amenable to local treatment methods. General fatigue, poor appetite and pain are regarded as common and unavoidable side effect experienced during the course of cancer and its treatment. Anorexia is a common cause of malnutrition and is associated with negative effects on the quality of life (QOL) for patients with cancer. However, quality of life as a prognostic factor for survival in hepatocellular carcinoma. Management of appetite is the key to improving both the QOL and the prognosis for such patients.

Cancer-related anorexia and target therapy-induced anorexia is very important in HCC patients. According to Chinese medicine theory., "spleen-deficiency, qi-stagnation and dampness" are the most common syndrome in advanced hepatocellular carcinoma patients. Thus, the principles of Chinese medicine treatment are invigorating Pi, regulating qi, dissipating dampness and appetizing wei. Most patients received traditional Chinese medicine treatment as adjuvant therapy to alleviate cancer symptoms, diminishing the side effects and complications of treatment course at late stages. The purpose of the study was search the safety and efficacy of the of Xiang Sha Liu Jun Zi Decoction (XSLJZ) in advanced hepatocellular carcinoma patients with multiple protein kinase inhibitor therapy. Evaluate the treatment effect on the symptoms of appetite and quality of life in advanced hepatocellular carcinoma patients

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Advanced hepatocellular carcinoma patient
  • use multiple protein kinase inhibitor therapy paid by National Health Care Insurance system (NHCIS) in Taiwan
  • Child-Pugh A class
  • Eastern Cooperative Oncology Group performance status of 0-2
  • survival period over 3 months
  • used Xiang Sha Liu Jun Zi Decoction for one month before the multiple protein kinase inhibitor therapystarting point

Exclusion criteria

  • combine other cancer at the same time
  • ESRD under dialysis
  • heart disease,CHF、CAD、arrhythmia、hypertension (SBP>150mmHg,DSP>90 mmHg)
  • current serious infection
  • GI bleeding within 30 days
  • receive organ transplant
  • Child-Pugh Class B or C liver status。
  • Refractory Ascites in Liver Cirrhosis

Treatment and study plan

Xiang Sha Liu Jun Zi Decoction dry powder

Drug

the principles of Chinese medicine treatment areinvigorating Pi, regulating qi, dissipating dampness and appetizing wei

XSLJZ Placebo

Drug

XSLJZ Placebo

Primary outcomes

  1. body weight

    Time frame: 8 weeks

    patient body weight

  2. EORTC QLQ-C30 score

    Time frame: 8 weeks

    European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire score

  3. EORTC QLQ-HCC18

    Time frame: 8 weeks

    European Organization for Research and Treatment of Hepatocellular carcinoma Core Quality of Life Questionnaire score

  4. CASQ

    Time frame: 8 weeks

    cancer appetite and symptom questionnaire

  5. FACT-G

    Time frame: 8 weeks

    Functional Assessment of Cancer Therapy - General

Secondary outcomes

  1. CCMQ

    Time frame: 8 weeks

    Chinese medicine questionnaire

  2. tong diagnosis

    Time frame: 8 weeks

    tong diagnosis by Automatic Tongue Diagnosis System

  3. pulse diagnosis

    Time frame: 8 weeks

    pulse diagnosis by Huang's Sphygmography in Frequeny-domained Parameters

Sponsors and collaborators

Lead sponsor

China Medical University Hospital

Other

Registry information

Important dates

Study start
2020
Primary completion
2020
Study completion
2023
First posted
Sep 24, 2020
Registry last updated
May 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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