Hepatocellular CarcinomaNCT04555265
Cytokine Change in Hepatocellular Carcinoma Treated by Thermal Ablation
A study testing Radiofrequency ablation or microwave ablation in people with Hepatocellular Carcinoma, run by Chinese University of Hong Kong at 1 site in Hong Kong.
Trial summary
Background: Hepatocellular carcinoma (HCC) is the most common primary liver cancer with aggressive tumor behavior. Radiofrequency ablation (RFA) or microwave ablation (MWA) is an effective curative treatment for early stage HCC. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Hepatocellular Carcinoma
- What is being tested?
- Radiofrequency ablation or microwave ablation
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteHong Kong
- Study dates
- 1 Sep 2020to 31 Jul 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Consecutive patients with HCC undergoing RFA or MWA will be recruited into this study provided the following criteria are fulfilled.
- HCC of maximal diameter < 8cm, and/or
- Multiple tumor nodules < 5, and/or
- Normal liver (serum total bilirubin level < 50 umol/L and serum albumin > 30 g/L) and renal function (serum creatinine level <120 mmol/L)
- Child-Pugh class A or B
Who cannot join
- Evidence of extrahepatic metastasis
- Patients receiving combined hepatectomy and other local ablative therapy
- Patients with decompensated liver function that preclude local ablative treatment.
- Patients with previous treatment for HCC (TACE, radiofrequency ablation, high intensity focus ultrasound or systemic chemotherapy)
- Patients with inadequate serum sample for cytokine analysis
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Investigation of Cytokine Change and Its Prognostic Value in Patients With Hepatocellular Carcinoma Treated by Thermal Ablation
Background: Hepatocellular carcinoma (HCC) is the most common primary liver cancer with aggressive tumor behavior. Radiofrequency ablation (RFA) or microwave ablation (MWA) is an effective curative treatment for early stage HCC. This thermal ablation of liver tumor induces host immune response with changes in serum concentration of various cytokines. It is not clear whether this host immune response correlates with tumor recurrence and long-term patient survival.
Objective: This prospective study is to investigate the change of cytokines' level following RFA or MWA for HCC and its clinical correlation with tumor recurrence and patients' long-term survival data.
Read more
Hypothesis: Thermal ablation of HCC creates tumor antigen source for the generation of antitumor immunity and enhances host immune responses. The resulting inflammation and changes in cytokines may augment tumor cell death by increasing neutrophil infiltration and oxidative burst mechanisms. On the other hand, there may be negative effects via the production of growth factors, which could stimulate tumor cell growth within the sub-lethal margin. Therefore, the ultimate clinical consequences would be significantly affected by these immune responses.
Study design: This is a prospective study on the measurement of changes of serum cytokines in patients with HCC undergone RFA or MWA using the commercially available kit (MILLIPEX, Human cytokine/chemokine magnetic bead panel - Immunology Multiplex Assay ), which measure 10 cytokines, including IL-1β, IL-6, IL-10, IL-12 (p40), IL-12 (p70), TNF-α, CXCL8, CXCL9, CXCL10, CCL2, CCL5. Statistical correlation will be performed between the cytokine change and long-term patients' clinical outcome using the prospectively collected database.
Subjects: Patients with HCC undergone RFA or MWA in the Department of Surgery, The Chinese University of Hong Kong will be recruited. Exclusion criteria were evidence of extrahepatic metastasis, patients receiving combined hepatectomy and other local ablative therapy and patients with decompensated liver function that preclude local ablative treatment.
Intervention: RFA or MWA will be performed for patients with HCC. The serum samples of all consecutive recruited patients will be collected prospectively during the intervention. The measurement of cytokines level will be performed in the Laboratory of Department of Chemical Pathology, The Chinese University of Hong Kong under the standard protocol.
Main outcome measures: Primary outcome measure is early intrahepatic tumor recurrence within one year after thermal ablation. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Data analysis: All data will be prospectively collected by a research assistant and computerized in a database. Statistical analysis will be performed by Chi-square test or Fisher's exact test, where appropriate, to compare discrete variables and Mann-Whitney U test to compare continuous variables. Cumulative survival will be computed by the Kaplan-Meier method and compared by Log-rank test. Multivariable analysis using logistic regression model will be done to identify the independent prognostic factors affecting early tumor recurrence.
Expected results: Understanding the relationship between the cytokines change during thermal ablation and post-treatment tumor recurrence helps to identify high risk patients for the possible adjuvant therapy in future study.
Read the detailed description
Background Liver cancer is the sixth most common malignancy in the world. It is the fourth leading cause of cancer-related deaths and has a global incidence of more than 840,000 new cases in 2018.1 Hepatocellular carcinoma (HCC) accounts for 75% - 85% of primary liver cancer. Hepatectomy, radiofrequency ablation (RFA) and orthotopic liver transplantation are the main treatment options for patients with early stage HCC.2 Hepatectomy is only indicated in patients with early stage HCC and preserved liver function, whereas the application of liver transplantation is limited globally because of organ shortage. RFA is therefore the most effective treatment in patients with HCC and borderline liver function due to cirrhotic liver, especially in Asia-Pacific region where hepatitis B infection is prevalent.
Thermal ablation kills tumors via direct thermal denaturation and coagulation of tumor proteins.3 The retention of devitalized and damaged tumor cells within the body stimulates a robust inflammatory response. It has also been reported that thermal ablation creates a tumor antigen source for the generation of antitumor immunity and enhances host immune responses.4 Activated platelets release interleukin (IL) -1, tumor necrosis factor (TNF), and transforming growth factor , which increase vascular permeability and promote chemotaxis. Neutrophils are attracted to the ablation site and perform debris scavenging by releasing free radicals via oxidative burst mechanisms aimed at destroying inciting agents. Macrophage migration ensues, transitioning to the proliferative stage, during which macrophages secrete growth factors, including TNF, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor.5 The level of proliferative activity of macrophages and lymphocytes is mediated by IL-6 positively and IL-10 negatively.6, 7 In the event of an incomplete ablation or nearly complete ablation, viable tumor cells in the sub-lethal ablation zone) may be affected positively or negatively by the concomitant inflammatory response including increased levels of cytokines and growth factors. Inflammation following ablation may have negative effects via the production of growth factors and cytokines by macrophages and lymphocytes, which could stimulate tumor cell growth within the sub-lethal zone.8 Human and animal studies using immunohistochemical staining of tissues, enzyme-linked immunosorbent assay of tissue lysates, and enzyme-linked immunosorbent assay of plasma have shown significant increase in specific inflammatory and immunomodulatory mediators after RFA.9, 10 The principle investigator has previously reported the inflammatory responses of RFA using the porcine liver model that the level of systemic inflammatory markers (TNF and IL-1) was significantly elevated after RFA, when compared with hepatectomy.11 Although pre-clinical studies on inflammatory responses of thermal ablation for liver tumor are substantial, clinical correlation of these micro-environmental reaction is limited in the literature. Erinjeri et al.12 reported that the ablation type and primary diagnosis predicted the change of IL-6 and patient age predicted the change of IL-10 after thermal ablation of tumors. IL-6 may act as surrogates for immunogenic cell death and the combination of immunogenic death-inducing procedures with immune check-point inhibitor may be beneficial to prolong patient survival after RFA.13 At the cellular level, RFA has proven to enhance tumor-associated antigen-specific T cell response and this contributes to the HCC recurrence-free survival of patients.14 Nonetheless, it is still not clear about the possible relationship between RFA-induced cytokines change and its prognostic value on tumor recurrence and long-term patient survival.
The principle investigator has reported the results of 209 patients receiving RFA as the sole treatment for HCC.15 The overall tumor recurrence rate was up to 80% with median follow-up of 26 months. Hence, identification of high-risk patients who might develop early recurrence using surrogate biomarkers (e.g. cytokines) carries an important clinical implication on the use of adjuvant treatment (e.g. immune check-point inhibitor).
Therefore, the investigators propose this single-center prospective study to analysis the change in serum cytokines level in patients with HCC treated by RFA or MWA. The result will be used to correlate the clinical outcome of patients, especially tumor recurrence and long-term survival outcome. This proposed clinical trial is of clinical importance in establishing the potential role of immune response as surrogate biomarkers to predict long-term patient outcome. It establishes the platform for future study of adjuvant treatment using immune check-point inhibitor for patients with HCC treated by RFA or other thermal ablative therapy. The investigators' center is a tertiary referral center in Hong Kong managing patients with complicated hepatobiliary and pancreatic diseases. The number of new cases of patients with HCC managed in the investigators' center is around 200 every year and the number of patients with HCC undergoing hepatectomy is around 80 every year. All the investigators are experts with vast experience in clinical and basic researches of patients with HCC. The investigators have conducted and published several randomized trials on management of HCC and other aspects of hepatobiliary surgery in international journals.16-19
Hypothesis RFA or MWA for HCC might induce inflammatory immune response with resulting change in cytokines level. This micro-environmental reaction might positively or negatively regulate the residual tumor cells, leading to the significant changes in tumor recurrence and long-term patient survival.
Aim of study This prospective study aims to investigate the change of cytokines' level following RFA or MWA for HCC and its clinical correlation with tumor recurrence and patients' long-term survival data. Primary outcome measure is early tumor recurrence within one year after RFA. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Primary outcome measure is early intrahepatic tumor recurrence within one year after RFA and MWA. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Analysis of cytokines level using studied patient serum samples
Analytes available:
IL-1β, IL-6, IL-10, IL-12 (p40), IL-12 (p70), TNF-α, CXCL8, CXCL9, CXCL10, CCL2, CCL5
Commercially available kit:
MILLIPLEX MAP Human Cytokine/Chemokine Magnetic Bead Panel - Immunology Multiplex Assay
Application of kit:
Simultaneously analyze multiple cytokine and chemokine biomarkers with MILLIPLEX MAP Human Cytokine/Chemokine Magnetic Bead Panel - Immunology Multiplex Assay, in human serum, plasma and cell culture samples. This is an overnight incubation assay.
Expected time of study The investigators' institution is a major tertiary referral center for HCC in Hong Kong. The patient recruitment will be started once the approval from Institution Review Board is obtained. The recruitment period is around 12 months to 18 months. With the median follow-up period of around 18 months, It is expected that the total period of study is three years.
Sample size estimation Expected number of patients to be recruited is estimated at 60 according to the past patient number undergoing treatment under the department.
Statistical analysis All data will be prospectively collected by a research assistant and computerized in a database. Statistical analysis will be performed by Chi-square test or Fisher's exact test, where appropriate, to compare discrete variables and Mann-Whitney U test to compare continuous variables. Cumulative survival will be computed by the Kaplan-Meier method and compared by Log-rank test. Multivariable analysis using logistic regression model will be done to identify the independent prognostic factors affecting early tumor recurrence.
Ethical Consideration This study will be carried out in accordance with the Declaration of Helsinki of the World Medical Association and the International Conference on Harmonization - Good Clinical Practice.
Consent Written voluntary consent will be obtained after full explanation of the trial to the patient before operation and randomization.
Relevance to clinical applications
This study carries significant clinical influence on the surgical management of patient with HCC. Since hepatitis B infection is still endemic in Asia-Pacific area like Hong Kong, hepatitis B related HCC is still a burden among the whole pool of cancer patients. This study aims to establish the potential role of immune response as surrogate biomarkers to predict long-term patient outcome. It enhances the development of the platform for future study of adjuvant treatment using immune check-point inhibitor for patients with HCC treated by thermal ablative therapy.
- Conditions
- Hepatocellular Carcinoma
- Being tested
- Radiofrequency ablation or microwave ablation
- Keywords
- cytokine, hepatocellular, carcinoma, thermal, ablation
- Medical subject headings
- Carcinoma, Hepatocellular, Carcinoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Radiofrequency ablation or microwave ablationDevice
Hepatocellular carcinoma treated by either radiofrequency ablation or microwave ablation
| Study group | Role | What they receive |
|---|---|---|
| Thermal ablation group | Other | Patients with hepatocellular carcinoma treated by thermal ablation Receives: Device: Radiofrequency ablation or microwave ablation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Early tumor recurrence
Early intrahepatic tumor recurrence within one year after RFA and MWA
Measured: 12 months
Secondary outcomes (1)
Other tutor recurrence
Late intrahepatic recurrence and extrahepatic metastasis
Measured: up to 24 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Sep 2020
- Study start1 Sep 2020
- Primary completion31 Jul 2023
- Study completion31 Jul 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hepatocellular CarcinomaStudies of the same condition, open and under way.
- More trials run by Chinese University of Hong KongThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Patients with hepatocellular carcinoma treated by thermal ablation
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Chinese University of Hong Kong
- Sponsor type
- University, hospital or other
- Collaborators
- The Hong Kong Society of Gastroenterology
- Responsible party
- Principal investigator, Kelvin K.C. Ng, Chinese University of Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04555265
- Sponsor's protocol ID
- 001kkcng/surg/cuhk
- Status last verified
- Aug 2023
- First submitted
- 11 Sep 2020
- Last updated
- 31 Aug 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Aug 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigation of Cytokine Change and Its Prognostic Value in Patients With Hepatocellular Carcinoma Treated by Thermal Ablation
- ClinicalTrials.gov ID
- NCT04555265
- Acronym / sponsor ID
- 001kkcng/surg/cuhk
- Conditions
- Hepatocellular Carcinoma
- Keywords
- cytokine, hepatocellular, carcinoma, thermal, ablation
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Chinese University of Hong KongUniversity, hospital or other
- Collaborators
- The Hong Kong Society of Gastroenterology
- Study start
- 1 Sep 2020 (actual)
- Primary completion
- 31 Jul 2023 (actual)
- Study completion
- 31 Jul 2023 (actual)
- First posted
- 18 Sep 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background: Hepatocellular carcinoma (HCC) is the most common primary liver cancer with aggressive tumor behavior. Radiofrequency ablation (RFA) or microwave ablation (MWA) is an effective curative treatment for early stage HCC. This thermal ablation of liver tumor induces host immune response with changes in serum concentration of various cytokines. It is not clear whether this host immune response correlates with tumor recurrence and long-term patient survival.
Objective: This prospective study is to investigate the change of cytokines' level following RFA or MWA for HCC and its clinical correlation with tumor recurrence and patients' long-term survival data.
Hypothesis: Thermal ablation of HCC creates tumor antigen source for the generation of antitumor immunity and enhances host immune responses. The resulting inflammation and changes in cytokines may augment tumor cell death by increasing neutrophil infiltration and oxidative burst mechanisms. On the other hand, there may be negative effects via the production of growth factors, which could stimulate tumor cell growth within the sub-lethal margin. Therefore, the ultimate clinical consequences would be significantly affected by these immune responses.
Study design: This is a prospective study on the measurement of changes of serum cytokines in patients with HCC undergone RFA or MWA using the commercially available kit (MILLIPEX, Human cytokine/chemokine magnetic bead panel - Immunology Multiplex Assay ), which measure 10 cytokines, including IL-1β, IL-6, IL-10, IL-12 (p40), IL-12 (p70), TNF-α, CXCL8, CXCL9, CXCL10, CCL2, CCL5. Statistical correlation will be performed between the cytokine change and long-term patients' clinical outcome using the prospectively collected database.
Subjects: Patients with HCC undergone RFA or MWA in the Department of Surgery, The Chinese University of Hong Kong will be recruited. Exclusion criteria were evidence of extrahepatic metastasis, patients receiving combined hepatectomy and other local ablative therapy and patients with decompensated liver function that preclude local ablative treatment.
Intervention: RFA or MWA will be performed for patients with HCC. The serum samples of all consecutive recruited patients will be collected prospectively during the intervention. The measurement of cytokines level will be performed in the Laboratory of Department of Chemical Pathology, The Chinese University of Hong Kong under the standard protocol.
Main outcome measures: Primary outcome measure is early intrahepatic tumor recurrence within one year after thermal ablation. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Data analysis: All data will be prospectively collected by a research assistant and computerized in a database. Statistical analysis will be performed by Chi-square test or Fisher's exact test, where appropriate, to compare discrete variables and Mann-Whitney U test to compare continuous variables. Cumulative survival will be computed by the Kaplan-Meier method and compared by Log-rank test. Multivariable analysis using logistic regression model will be done to identify the independent prognostic factors affecting early tumor recurrence.
Expected results: Understanding the relationship between the cytokines change during thermal ablation and post-treatment tumor recurrence helps to identify high risk patients for the possible adjuvant therapy in future study.
Detailed description
Background Liver cancer is the sixth most common malignancy in the world. It is the fourth leading cause of cancer-related deaths and has a global incidence of more than 840,000 new cases in 2018.1 Hepatocellular carcinoma (HCC) accounts for 75% - 85% of primary liver cancer. Hepatectomy, radiofrequency ablation (RFA) and orthotopic liver transplantation are the main treatment options for patients with early stage HCC.2 Hepatectomy is only indicated in patients with early stage HCC and preserved liver function, whereas the application of liver transplantation is limited globally because of organ shortage. RFA is therefore the most effective treatment in patients with HCC and borderline liver function due to cirrhotic liver, especially in Asia-Pacific region where hepatitis B infection is prevalent.
Thermal ablation kills tumors via direct thermal denaturation and coagulation of tumor proteins.3 The retention of devitalized and damaged tumor cells within the body stimulates a robust inflammatory response. It has also been reported that thermal ablation creates a tumor antigen source for the generation of antitumor immunity and enhances host immune responses.4 Activated platelets release interleukin (IL) -1, tumor necrosis factor (TNF), and transforming growth factor , which increase vascular permeability and promote chemotaxis. Neutrophils are attracted to the ablation site and perform debris scavenging by releasing free radicals via oxidative burst mechanisms aimed at destroying inciting agents. Macrophage migration ensues, transitioning to the proliferative stage, during which macrophages secrete growth factors, including TNF, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor.5 The level of proliferative activity of macrophages and lymphocytes is mediated by IL-6 positively and IL-10 negatively.6, 7 In the event of an incomplete ablation or nearly complete ablation, viable tumor cells in the sub-lethal ablation zone) may be affected positively or negatively by the concomitant inflammatory response including increased levels of cytokines and growth factors. Inflammation following ablation may have negative effects via the production of growth factors and cytokines by macrophages and lymphocytes, which could stimulate tumor cell growth within the sub-lethal zone.8 Human and animal studies using immunohistochemical staining of tissues, enzyme-linked immunosorbent assay of tissue lysates, and enzyme-linked immunosorbent assay of plasma have shown significant increase in specific inflammatory and immunomodulatory mediators after RFA.9, 10 The principle investigator has previously reported the inflammatory responses of RFA using the porcine liver model that the level of systemic inflammatory markers (TNF and IL-1) was significantly elevated after RFA, when compared with hepatectomy.11 Although pre-clinical studies on inflammatory responses of thermal ablation for liver tumor are substantial, clinical correlation of these micro-environmental reaction is limited in the literature. Erinjeri et al.12 reported that the ablation type and primary diagnosis predicted the change of IL-6 and patient age predicted the change of IL-10 after thermal ablation of tumors. IL-6 may act as surrogates for immunogenic cell death and the combination of immunogenic death-inducing procedures with immune check-point inhibitor may be beneficial to prolong patient survival after RFA.13 At the cellular level, RFA has proven to enhance tumor-associated antigen-specific T cell response and this contributes to the HCC recurrence-free survival of patients.14 Nonetheless, it is still not clear about the possible relationship between RFA-induced cytokines change and its prognostic value on tumor recurrence and long-term patient survival.
The principle investigator has reported the results of 209 patients receiving RFA as the sole treatment for HCC.15 The overall tumor recurrence rate was up to 80% with median follow-up of 26 months. Hence, identification of high-risk patients who might develop early recurrence using surrogate biomarkers (e.g. cytokines) carries an important clinical implication on the use of adjuvant treatment (e.g. immune check-point inhibitor).
Therefore, the investigators propose this single-center prospective study to analysis the change in serum cytokines level in patients with HCC treated by RFA or MWA. The result will be used to correlate the clinical outcome of patients, especially tumor recurrence and long-term survival outcome. This proposed clinical trial is of clinical importance in establishing the potential role of immune response as surrogate biomarkers to predict long-term patient outcome. It establishes the platform for future study of adjuvant treatment using immune check-point inhibitor for patients with HCC treated by RFA or other thermal ablative therapy. The investigators' center is a tertiary referral center in Hong Kong managing patients with complicated hepatobiliary and pancreatic diseases. The number of new cases of patients with HCC managed in the investigators' center is around 200 every year and the number of patients with HCC undergoing hepatectomy is around 80 every year. All the investigators are experts with vast experience in clinical and basic researches of patients with HCC. The investigators have conducted and published several randomized trials on management of HCC and other aspects of hepatobiliary surgery in international journals.16-19
Hypothesis RFA or MWA for HCC might induce inflammatory immune response with resulting change in cytokines level. This micro-environmental reaction might positively or negatively regulate the residual tumor cells, leading to the significant changes in tumor recurrence and long-term patient survival.
Aim of study This prospective study aims to investigate the change of cytokines' level following RFA or MWA for HCC and its clinical correlation with tumor recurrence and patients' long-term survival data. Primary outcome measure is early tumor recurrence within one year after RFA. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Primary outcome measure is early intrahepatic tumor recurrence within one year after RFA and MWA. Secondary outcome measures are other tumor recurrence pattern (late intrahepatic recurrence and extrahepatic metastasis), overall survival and recurrence-free survival.
Analysis of cytokines level using studied patient serum samples
Analytes available:
IL-1β, IL-6, IL-10, IL-12 (p40), IL-12 (p70), TNF-α, CXCL8, CXCL9, CXCL10, CCL2, CCL5
Commercially available kit:
MILLIPLEX MAP Human Cytokine/Chemokine Magnetic Bead Panel - Immunology Multiplex Assay
Application of kit:
Simultaneously analyze multiple cytokine and chemokine biomarkers with MILLIPLEX MAP Human Cytokine/Chemokine Magnetic Bead Panel - Immunology Multiplex Assay, in human serum, plasma and cell culture samples. This is an overnight incubation assay.
Expected time of study The investigators' institution is a major tertiary referral center for HCC in Hong Kong. The patient recruitment will be started once the approval from Institution Review Board is obtained. The recruitment period is around 12 months to 18 months. With the median follow-up period of around 18 months, It is expected that the total period of study is three years.
Sample size estimation Expected number of patients to be recruited is estimated at 60 according to the past patient number undergoing treatment under the department.
Statistical analysis All data will be prospectively collected by a research assistant and computerized in a database. Statistical analysis will be performed by Chi-square test or Fisher's exact test, where appropriate, to compare discrete variables and Mann-Whitney U test to compare continuous variables. Cumulative survival will be computed by the Kaplan-Meier method and compared by Log-rank test. Multivariable analysis using logistic regression model will be done to identify the independent prognostic factors affecting early tumor recurrence.
Ethical Consideration This study will be carried out in accordance with the Declaration of Helsinki of the World Medical Association and the International Conference on Harmonization - Good Clinical Practice.
Consent Written voluntary consent will be obtained after full explanation of the trial to the patient before operation and randomization.
Relevance to clinical applications
This study carries significant clinical influence on the surgical management of patient with HCC. Since hepatitis B infection is still endemic in Asia-Pacific area like Hong Kong, hepatitis B related HCC is still a burden among the whole pool of cancer patients. This study aims to establish the potential role of immune response as surrogate biomarkers to predict long-term patient outcome. It enhances the development of the platform for future study of adjuvant treatment using immune check-point inhibitor for patients with HCC treated by thermal ablative therapy.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Patients with hepatocellular carcinoma treated by thermal ablation
| Arm | Type | Receives |
|---|---|---|
| Thermal ablation group | Other | Device: Radiofrequency ablation or microwave ablationPatients with hepatocellular carcinoma treated by thermal ablation |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Consecutive patients with HCC undergoing RFA or MWA will be recruited into this study provided the following criteria are fulfilled.
Key exclusion criteria (5 listed)
- Evidence of extrahepatic metastasis
- Patients receiving combined hepatectomy and other local ablative therapy
- Patients with decompensated liver function that preclude local ablative treatment.
- Patients with previous treatment for HCC (TACE, radiofrequency ablation, high intensity focus ultrasound or systemic chemotherapy)
- Patients with inadequate serum sample for cytokine analysis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Radiofrequency ablation or microwave ablationHepatocellular carcinoma treated by either radiofrequency ablation or microwave ablation | Device | Thermal ablation group |
Primary outcome
Early tumor recurrence
Time frame: 12 months
Early intrahepatic tumor recurrence within one year after RFA and MWA
1 secondary outcome
Other tutor recurrence
Time frame: up to 24 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Radiofrequency ablation or microwave ablation in people with Hepatocellular Carcinoma, run by Chinese University of Hong Kong at 1 site in Hong Kong.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 31 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Early tumor recurrence (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2023.