Hepatocellular CarcinomaAP-LAPONCT04852211
Laparoscopic Versus Open Major Hepatectomy for HCC Hepatectomy for Hepatocellular Carcinoma
A study testing Open or laparoscopic surgery 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 sixth most common malignancy in the world. Major hepatectomy (resection of > 3 liver segments) is needed if tumor is close to major blood vessels within liver. 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?
- Open or laparoscopic surgery
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 212 participants
- Where
- 1 siteHong Kong
- Study dates
- 1 Dec 2021to 30 Nov 2024
- 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
- Diagnosis of HCC is in accordance to the diagnostic criteria for HCC used by the European Association for the Study of the Liver. HCC was diagnosed when the radiologic imaging techniques (spiral contrasted CT scan or contrasted MRI) showed typical features of HCC (contrast enhancement in the arterial phase and rapid wash-out of contrast in the venous or delayed phase) and/or elevated serum alpha fetoprotein (AFP) level.
- HCC of maximum diameter up to 10 cm; Single or multiple tumor nodules confined to one liver lobe according to the previous reported series
- Major hepatectomy (resection of > 3 Couinaud's segments) is required as judged by hepatobiliary surgeons
- Absence of extrahepatic metastasis or radiological evidence of venous invasion of major portal vein or hepatic vein branches
- Child's A liver function
- Indocyanine green retention at 15 min (ICG-15) < 15%
- Adequate future liver remnant (image-guided volumetry > 35% of estimated standard liver volume)
- General condition fit for general anaesthesia
Who cannot join
- Tumors unfavorable for major hepatectomy (e.g. bilobar tumors, main portal vein tumor thrombus and/or inadequate future liver volume)
- Previous treatment for HCC (e.g. transarterial chemoembolization, or chemotherapy)
- Tumors require combined hepatectomy and thermal ablation therapy
Trial locations and contacts
1 site in 1 country.
Hong Kong1 site, 1 recruiting
- Recruiting
Chinese University of Hong Kong
Hong Kong
Kelvin K.C. Ng, MS, PhD, +85291242695, kelvinng@surgery.cuhk.edu.hk
About this study
Official title: Asia-Pacific Multi-Centre Randomized Trial of Laparoscopic Versus Open Major Hepatectomy for Hepatocellular Carcinoma (AP-LAPO Trial)
Background: Hepatocellular carcinoma (HCC) is the sixth most common malignancy in the world. Major hepatectomy (resection of > 3 liver segments) is needed if tumor is close to major blood vessels within liver. Despite low mortality, open major hepatectomy (OMH) is associated with high tumor recurrence rate, and short survival. Immunosuppression due to surgical stress and blood transfusion, and dissemination of tumor cells because of tumor manipulation all contribute to tumor recurrence.
Laparoscopic major hepatectomy (LMH) is a newly developed minimally invasive technique for HCC. Apart from less wound problems and shorter recovery time than open surgery, LMH may have potential oncological benefits of prolonging survival. These could be related to the reduced intraoperative blood loss, less immunosuppression due to surgical stress, and less tumor manipulation. Hence, LMH could be a better treatment option than OMH for HCC.
Read more
Objectives:
- To compare the long-term oncological outcome between laparoscopic and open major hepatectomy for patients with hepatocellular carcinoma
- To achieve the comparison under the study design of multi-center randomized trial involving 5 high-volume centers in Asia-Pacific region
- Primary outcome is 2-year recurrence-free survival.
- Secondary outcome as intraoperative blood loss, blood transfusion, 30-day and hospital mortality, postoperative morbidities according Clavien-Dindo classification, hospital stay, quality of life, overall and recurrence-free survival rates up to 5 years after surgery
- To compare the perioperative changes in stress-related cytokines, which help to clarify the stress response and immunosuppression and their correlations with overall and recurrence-free survival rates
Hypothesis: Laparoscopic major hepatectomy is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than open major hepatectomy.
Study design: This is an open-labelled prospective randomized trial involving 106 patients in each treatment arm (Total number of patients recruited: 212). The study will involve 5 surgery centers in Asia-Pacific region (2 centers in Hong Kong, 3 centers in Mainland China Foshan, Shanghai and Sichuan).
Subjects: Patients with HCC undergone major hepatectomy. Recruitment centres involved:
- Department of Surgery, The Chinese University of Hong Kong
- Department of Surgery, Kwong Wah Hospital, Hong Kong
- Department of Surgery, West China Medical School of Sichuan University
- Department of Biliary Surgery, Eastern Hepatobiliary Surgery Hospital \& Institute, Second Military Medical University
- Department of Surgery, The First People's Hospital of Foshan
Intervention: Consented patient will be randomized 1:1 to one of the two treatment arms:
- Laparoscopic group: LMH
- Open group: OMH The randomization schedule will be generated by the Clinical Trials Centre (CTC) of principle investigator's center, prior to the start of the study.
Main outcome measure: The primary objective is to test the hypothesis that LMH is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than OMH. The primary outcome measure is 2-year recurrence-free survival.
Data analysis: Statistical plan and data monitoring Statistical analysis will be performed using SPSS version 11.0 (SPSS Inc., Chicago, Ill). The 2-year recurrence-free survival (primary outcome) will be evaluated by Kaplan-Meier method and compared by the log-rank test between studied groups.
Expected results: The result of this study provides level 1 evidence on the best treatment option for HCC, which needs major hepatectomy. Such information will influence the evidence-based policy in professional practice in the management algorithm for HCC. Since postoperative complications and tumor recurrence are substantial after OMH, potential benefits of LMH tested in this study will help to alleviate these problems.
Read the detailed description
Background: Hepatocellular carcinoma (HCC) is the sixth most common malignancy in the world.The practice of screening by ultrasonography and serum alpha-fetoprotein concentration in cirrhotic patients and hepatitis B carriers has led to an increasing incidence of HCC.
Hepatectomy, local ablation and liver transplantation are regarded as the mainstay of curative treatment for HCC according to international guidelines by EASL, AASLD and ESMO.The shortage of liver grafts has limited the application of liver transplantation. Hepatectomy is thus widely accepted as the treatment option of choice for patients with HCC and non cirrhotic liver.
Major hepatectomy (resection of > 3 Couinaud's segments) is always needed when HCC is large or is close to major blood vessels within liver. With the advancements in techniques of hepatectomy and perioperative patient care, the operative mortality of open major hepatectomy (OMH) has reduced to < 5% in recent years. Nonetheless, OMH for HCC is still associated with major problems as follows:
- It is associated with significant morbidities. The morbidity rate after OMH remains high (30% - 40%) even in high-volume centres. Wound infection and bronchopneumonia are among the most common complications after hepatic resection. Long incision and vigorous retraction of the rib cage are required to achieve adequate exposure of the liver tumor during hepatic resection. As a result, sepsis due to chest complications and wound problems are frequently encountered. Furthermore, division of the porto-systemic collaterals in the anterior abdominal wall contributes to postoperative ascites, which is another common complication.
- It is associated with a high tumor recurrence rate, even when performed with a curative intent. The 3-year recurrence rate has been reported to be more than 50%. Most recurrences occur in the liver remnant, in the forms of intrahepatic metastasis or multicentric tumor recurrence. Risk factors related to recurrence include unfavorable tumor factors such as microscopic venous or capsular invasion. Hence, tumor cell dissemination could be the main mechanism of recurrence. In this context, manipulation of the tumor during OMH leading to tumor cell dissemination can potentially contribute to high tumor recurrence rate. Furthermore, it has been suggested that postoperative immunosuppression induced by surgical stress may induce tumor growth in the liver remnant.
Laparoscopy has a well-defined role in the staging and diagnosis of hepatobiliary malignancies. However, laparoscopic hepatectomy has not yet been widely practiced, because of the technical difficulties in liver resection, difficulty in the control of hemorrhage during liver transection and retraction of the liver for optimum exposure. With the advanced laparoscopic techniques, much enthusiasm has been developed in laparoscopic major hepatectomy (LMH). Recent series have proven the feasibility and safety of LMH for HCC. The selection criteria of the reported series included tumor size up to 10cm and single or multiple tumors confined to one liver lobe. The overall conversion rates was around 10%. There was no hospital mortality and the morbidity rate was about 10%. Apart from the documented advantages of laparoscopic surgery (less wound and chest complications, and shorter hospital stay), theoretically, LMH carries oncological advantages over OMH. LMH may result in less surgical stress and immunosuppression due to less intraoperative blood loss than OMH. Moreover, using laparoscopic instruments, it involves minimal manipulation of the tumor and less cancer cells dissemination during surgery. Potentially, postoperative tumor recurrence could be reduced and hence patient survival could be prolonged.
To date, only retrospective studies using propensity score matching to compare LMH with OMH were reported. In these study, the studied patient number was small (< 40) in each matched treatment arm and the reported 2-year overall (86% - 88% vs. 85% - 100%) and recurrence-free survival (72% - 83% vs. 81% - 85%) rates were comparable between OMH and LMH. Nevertheless, there is a trend that LMH is associated with better overall and recurrence-free survival than OMH. It is likely that these studies were underpowered (Type II error) to show the potential oncological benefits of LMH over OMH. Because of these limited data on LMH, according to EASL, AASLD and ESMO guidelines, its role for HCC is still not yet defined. In the sphere of laparoscopic hepatectomy, according to the European Guideline Meeting for Laparoscopic Liver Surgery (Southampton consensus), there was only limited data on short-term outcome but no data on long-term outcome of LMH. With these reasons, there is an urge for a prospective study aiming to define the role of LMH for HCC with respect to its potential oncological benefits.
In the principle investigator's institution (the Department of Surgery, The Chinese University of Hong Kong), preliminary data using propensity score matching analysis on patients with HCC (median size = 4cm) undergone either laparoscopic (n = 112) or open hepatectomy (n = 224) (major hepatectomy accounts for 40.5%), the intraoperative blood loss (median: 159 mL vs. 419 mL), blood transfusion rate (0% vs. 4.5%) and morbidity rate (5.4% vs. 28.1%) were significantly lower in laparoscopic group than open group. The hospital mortality (0% vs. 0.4%), long-term overall (5-year: 56% vs. 42%) and recurrence free (5-year: 36% vs. 33%) survival rates were comparable between groups. (Supplementary information attached) With this experience, the principle investigator proposes an open labelled prospective multi-center randomized trial (AP-LAPO Trial) comparing LMH with OMH for HCC. This study involves 5 high-volume centres specialized in liver surgery and with facilities supporting LMH and OMH in Asia-Pacific region (Hong Kong, Sichuan, Guangzhou and Foshan). These centres perform at least 30 LMH or OMH per year (The Chinese University of Hong Kong, median no. = 51; Kwong Wah Hospital, median no. = 30; West China Medical School of Sichuan University, median no. 120; Eastern Hepatobiliary Surgery Hospital \& Institute, median no. = 115; The First People's Hospital of Foshan, median no. = 102), and have achieved excellent perioperative and oncological outcome after LMH or OMH (operative mortality 1% - 2%; complication rate 14% - 23%; 2-year overall survival rate 85% - 88%; 2-year disease-free survival rate 81% - 84%).
Objectives and hypothesis: The primary objective is to test the hypothesis that LMH is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than OMH. The primary outcome measure is 2-year recurrence-free survival. The secondary outcome measures include hospital mortality, morbidity, quality of life and overall survival between groups. Besides, stress-related cytokines (interleukin-6 [IL-6] and immunosuppressive acidic protein[IAP]) will also be measured during the perioperative
Sample size estimation: Based on a reported 2-year recurrence-free survival rate of 72% after OMH and an expected 88% after LMH (about 20% improvement) according to a previously reported series, 106 patients need to be recruited to each arm in order to demonstrate a statistically significant difference with a 80% power at the 0.05 level of 2-sided significant difference between laparoscopic and open hepatic resection, allowing a drop-out rate of 10%. This sample size will also allow detection of reduction of 2-year tumor recurrence from 50% in OMH group to 30% in LMH with a similar power and level of significance. The principle investigator's unit is a major referral center for management of HCC in Hong Kong, with more than 150 new cases seen per year. There are one other centers in Hong Kong and 3 centers in Mainland China, which are specialized in both laparoscopic and open surgery for patients with HCC, with referral patient number ranging from 50 to 200 per year. The planned number of patients recruited in each participating centres is as follows (The Chinese University of Hong Kong, N = 32; Kwong Wah Hospital, N = 20; West China Medical School of Sichuan University, N = 50; Eastern Hepatobiliary Surgery Hospital \& Institute, N = 50; The First People's Hospital of Foshan, median no. = 60) It is therefore expected that recruitment can be completed in about 12 months. All patients will be observed for at least 24 months after treatment. Hence, the total period of study including follow-up is estimated to be about 3 years for the funding period. After the funding period, recruited patients will be followed up periodically up to 5 years after surgery to evaluate the long-term outcome.
Statistical analysis: Statistical analysis will be performed using SPSS version 11.0 (SPSS Inc., Chicago, Ill). The 2-year recurrence-free survival (primary outcome) will be evaluated by Kaplan-Meier method and compared by the log-rank test between studied groups.
Other secondary outcome measures will be compared using Chi-squared test or Fisher's exact test for categorical variables, and Mann-Whitney U test for continuous variables between groups. Overall survival is again computed by the Kaplan-Meier method and compared by the log-rank test between groups. P < 0.05 is considered statistically significant.
Ethical consideration: All aspects of the study will be discussed with each subject during a phone interview or screening visit. An information sheet will be provided, and each subject will be given the opportunity to seek medical advice or to discuss the study with friends or family prior to involvement. Each volunteer will give written, informed consent, in accordance with the attached form, and the subjects will be free to withdraw from the study at any time. This study will be performed in accordance with the ethical standards of the Declaration of Helsinki of 1975 and its later versions. Ethics approval from the institutional review broad of individual center will be sought.
Relevance to clinical applications: The proposed study is an open-labelled prospective multi-center randomized trial investigating the potential benefits of laparoscopic major hepatectomy for hepatocellular carcinoma (HCC), as compared to conventional open surgery. It involves 5 high-volume surgery centers in the Asia-Pacific region, where the incidence of hepatocellular carcinoma is high. The result of this study provides level 1 evidence on the best treatment option for HCC, which needs major hepatectomy. Such information will influence the evidence-based policy in professional practice in the management algorithm for HCC. Since postoperative complications and tumor recurrence are substantial after OMH, potential benefits of LMH tested in this study will help to alleviate these problems. Ultimately, the long-term survival of patients with HCC could be improved.
- Conditions
- Hepatocellular Carcinoma
- Being tested
- Open or laparoscopic surgery
- Keywords
- Laparoscopic surgery, Open Surgery, Major hepatectomy, Hepatocellular carcinoma
- Medical subject headings
- Carcinoma, Hepatocellular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Open or laparoscopic surgeryProcedure or surgery
Patients, with their consent, will be recruited to participate by investigators after considering the inclusion and exclusion criteria. Treatment allocation to the eligible patients will follow a randomization schedule. A total of 212 subjects will be randomized 1:1 to one of the two treatment arms:
- Laparoscopic group: LMH
- Open group: OMH
| Study group | Role | What they receive |
|---|---|---|
| Open major hepatectomy | Active comparator | Resection of the tumor together with 3 or more liver segments using open standard techniques of hepatectomy Receives: Procedure: Open or laparoscopic surgery |
| Laparoscopic major hepatectomy | Active comparator | Resection of the tumor together with 3 or more liver segments using minimally invasive techniques of hepatectomy Receives: Procedure: Open or laparoscopic surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
2-year recurrence-free survival
The proportion of patients surviving without tumor recurrence as measured by postoperative images (CT or MRI) at 2 years
Measured: 2 years
Secondary outcomes (4)
Hospital mortality
Death of patient after index surgery within same hospital admission
Measured: 1 year
Morbidity
Complications of surgery as defined by Clavien-Dindo classification
Measured: 1 year
Quality of llife
Quality of life assessment by Functional Assessment of Cancer Therapy - General questionnaire (Score 0 - 108); high score means good performance status and vice versa
Measured: 1 year
5 - year Overall survival
Overall survival of patients after surgery at 5 years after surgery
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Apr 2021
- Study start1 Dec 2021
- Primary completion30 Nov 2024 (estimated)
- Study completion30 Nov 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (30)Papers the sponsor has linked to this study.
- 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
- Randomised
- Intervention model
- Parallel groups
- Model description
- Patients with hepatocellular carcinoma which undergone major hepatectomy will be randomized to either laparoscopic or open surgery group
- Masking
- None (open label)
- Enrolment
- 212 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Chinese University of Hong Kong
- Sponsor type
- University, hospital or other
- Collaborators
- Health and Medicine Research Fund
- Responsible party
- Principal investigator, Kelvin K.C. Ng, Chinese University of Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04852211
- Sponsor's protocol ID
- 002kkcng/surg/cuhk
- Acronym
- AP-LAPO
- Status last verified
- Aug 2023
- First submitted
- 14 Apr 2021
- Last updated
- 31 Aug 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
PubMed 30207593European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J Hepatol. 2018 Jul;69(1):182-236. doi: 10.1016/j.jhep.2018.03.019. Epub 2018 Apr 5. No abstract available.
PubMed 29628281Heimbach JK, Kulik LM, Finn RS, Sirlin CB, Abecassis MM, Roberts LR, Zhu AX, Murad MH, Marrero JA. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology. 2018 Jan;67(1):358-380. doi: 10.1002/hep.29086. No abstract available.
PubMed 28130846Vogel A, Cervantes A, Chau I, Daniele B, Llovet JM, Meyer T, Nault JC, Neumann U, Ricke J, Sangro B, Schirmacher P, Verslype C, Zech CJ, Arnold D, Martinelli E; ESMO Guidelines Committee. Hepatocellular carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018 Oct 1;29(Suppl 4):iv238-iv255. doi: 10.1093/annonc/mdy308. No abstract available.
PubMed 30285213Ng KK, Vauthey JN, Pawlik TM, Lauwers GY, Regimbeau JM, Belghiti J, Ikai I, Yamaoka Y, Curley SA, Nagorney DM, Ng IO, Fan ST, Poon RT; International Cooperative Study Group on Hepatocellular Carcinoma. Is hepatic resection for large or multinodular hepatocellular carcinoma justified? Results from a multi-institutional database. Ann Surg Oncol. 2005 May;12(5):364-73. doi: 10.1245/ASO.2005.06.004. Epub 2005 Mar 31.
PubMed 15915370Hao S, Fan P, Chen S, Tu C, Wan C. Anterior approach to improve the long-term outcome in patients with large-size hepatocellular carcinoma having liver resection. J Surg Oncol. 2016 Dec;114(7):872-878. doi: 10.1002/jso.24433. Epub 2016 Sep 16.
PubMed 27632953Lee KF, Cheung YS, Wong J, Chong CC, Wong JS, Lai PB. Randomized clinical trial of open hepatectomy with or without intermittent Pringle manoeuvre. Br J Surg. 2012 Sep;99(9):1203-9. doi: 10.1002/bjs.8863. Epub 2012 Jul 24.
PubMed 22828986Ng KKC, Chok KSH, Chan ACY, Cheung TT, Wong TCL, Fung JYY, Yuen J, Poon RTP, Fan ST, Lo CM. Randomized clinical trial of hepatic resection versus radiofrequency ablation for early-stage hepatocellular carcinoma. Br J Surg. 2017 Dec;104(13):1775-1784. doi: 10.1002/bjs.10677. Epub 2017 Nov 1.
PubMed 29091283Ng KK, Cheung TT, Pang HH, Wong TC, Dai JW, Ma KW, She WH, Kotewall CN, Lo CM. A simplified prediction model for early intrahepatic recurrence after hepatectomy for patients with unilobar hepatocellular carcinoma without macroscopic vascular invasion: An implication for adjuvant therapy and postoperative surveillance. Surg Oncol. 2019 Sep;30:6-12. doi: 10.1016/j.suronc.2019.05.017. Epub 2019 May 22.
PubMed 31500787Jarnagin WR, Delman K, Kooby D, Mastorides S, Zager J, Brennan MF, Blumgart LH, Federoff H, Fong Y. Neoadjuvant interleukin-12 immunogene therapy protects against cancer recurrence after liver resection in an animal model. Ann Surg. 2000 May;231(5):762-71. doi: 10.1097/00000658-200005000-00017.
PubMed 10767798Halls MC, Berardi G, Cipriani F, Barkhatov L, Lainas P, Harris S, D'Hondt M, Rotellar F, Dagher I, Aldrighetti L, Troisi RI, Edwin B, Abu Hilal M. Development and validation of a difficulty score to predict intraoperative complications during laparoscopic liver resection. Br J Surg. 2018 Aug;105(9):1182-1191. doi: 10.1002/bjs.10821. Epub 2018 May 8.
PubMed 29737513Chen K, Pan Y, Hu GY, Maher H, Zheng XY, Yan JF. Laparoscopic Versus Open Major Hepatectomy for Hepatocellular Carcinoma: A Meta-Analysis. Surg Laparosc Endosc Percutan Tech. 2018 Oct;28(5):267-274. doi: 10.1097/SLE.0000000000000567.
PubMed 30180140Xu HW, Liu F, Li HY, Wei YG, Li B. Outcomes following laparoscopic versus open major hepatectomy for hepatocellular carcinoma in patients with cirrhosis: a propensity score-matched analysis. Surg Endosc. 2018 Feb;32(2):712-719. doi: 10.1007/s00464-017-5727-2. Epub 2017 Jul 19.
PubMed 28726140Delvecchio A, Conticchio M, Ratti F, Gelli M, Anelli FM, Laurent A, Vitali GC, Magistri P, Assirati G, Felli E, Wakabayashi T, Pessaux P, Piardi T, Di Benedetto F, de'Angelis N, Briceno-Delgado J, Adam R, Cherqui D, Aldrighetti L, Memeo R. Laparoscopic major hepatectomy for hepatocellular carcinoma in elderly patients: a multicentric propensity score-based analysis. Surg Endosc. 2021 Jul;35(7):3642-3652. doi: 10.1007/s00464-020-07843-7. Epub 2020 Aug 3.
PubMed 32748269Yoon YI, Kim KH, Kang SH, Kim WJ, Shin MH, Lee SK, Jung DH, Park GC, Ahn CS, Moon DB, Ha TY, Song GW, Hwang S, Lee SG. Pure Laparoscopic Versus Open Right Hepatectomy for Hepatocellular Carcinoma in Patients With Cirrhosis: A Propensity Score Matched Analysis. Ann Surg. 2017 May;265(5):856-863. doi: 10.1097/SLA.0000000000002072.
PubMed 27849661
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
- Asia-Pacific Multi-Centre Randomized Trial of Laparoscopic Versus Open Major Hepatectomy for Hepatocellular Carcinoma (AP-LAPO Trial)
- ClinicalTrials.gov ID
- NCT04852211
- Acronym / sponsor ID
- AP-LAPO / 002kkcng/surg/cuhk
- Conditions
- Hepatocellular Carcinoma
- Keywords
- Laparoscopic surgery, Open Surgery, Major hepatectomy, Hepatocellular carcinoma
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 212 participants (estimated)
- Lead sponsor
- Chinese University of Hong KongUniversity, hospital or other
- Collaborators
- Health and Medicine Research Fund
- Study start
- 1 Dec 2021 (actual)
- Primary completion
- 30 Nov 2024 (estimated)
- Study completion
- 30 Nov 2024 (estimated)
- First posted
- 21 Apr 2021 (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 sixth most common malignancy in the world. Major hepatectomy (resection of > 3 liver segments) is needed if tumor is close to major blood vessels within liver. Despite low mortality, open major hepatectomy (OMH) is associated with high tumor recurrence rate, and short survival. Immunosuppression due to surgical stress and blood transfusion, and dissemination of tumor cells because of tumor manipulation all contribute to tumor recurrence.
Laparoscopic major hepatectomy (LMH) is a newly developed minimally invasive technique for HCC. Apart from less wound problems and shorter recovery time than open surgery, LMH may have potential oncological benefits of prolonging survival. These could be related to the reduced intraoperative blood loss, less immunosuppression due to surgical stress, and less tumor manipulation. Hence, LMH could be a better treatment option than OMH for HCC.
Objectives:
- To compare the long-term oncological outcome between laparoscopic and open major hepatectomy for patients with hepatocellular carcinoma
- To achieve the comparison under the study design of multi-center randomized trial involving 5 high-volume centers in Asia-Pacific region
- Primary outcome is 2-year recurrence-free survival.
- Secondary outcome as intraoperative blood loss, blood transfusion, 30-day and hospital mortality, postoperative morbidities according Clavien-Dindo classification, hospital stay, quality of life, overall and recurrence-free survival rates up to 5 years after surgery
- To compare the perioperative changes in stress-related cytokines, which help to clarify the stress response and immunosuppression and their correlations with overall and recurrence-free survival rates
Hypothesis: Laparoscopic major hepatectomy is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than open major hepatectomy.
Study design: This is an open-labelled prospective randomized trial involving 106 patients in each treatment arm (Total number of patients recruited: 212). The study will involve 5 surgery centers in Asia-Pacific region (2 centers in Hong Kong, 3 centers in Mainland China Foshan, Shanghai and Sichuan).
Subjects: Patients with HCC undergone major hepatectomy. Recruitment centres involved:
- Department of Surgery, The Chinese University of Hong Kong
- Department of Surgery, Kwong Wah Hospital, Hong Kong
- Department of Surgery, West China Medical School of Sichuan University
- Department of Biliary Surgery, Eastern Hepatobiliary Surgery Hospital \& Institute, Second Military Medical University
- Department of Surgery, The First People's Hospital of Foshan
Intervention: Consented patient will be randomized 1:1 to one of the two treatment arms:
- Laparoscopic group: LMH
- Open group: OMH The randomization schedule will be generated by the Clinical Trials Centre (CTC) of principle investigator's center, prior to the start of the study.
Main outcome measure: The primary objective is to test the hypothesis that LMH is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than OMH. The primary outcome measure is 2-year recurrence-free survival.
Data analysis: Statistical plan and data monitoring Statistical analysis will be performed using SPSS version 11.0 (SPSS Inc., Chicago, Ill). The 2-year recurrence-free survival (primary outcome) will be evaluated by Kaplan-Meier method and compared by the log-rank test between studied groups.
Expected results: The result of this study provides level 1 evidence on the best treatment option for HCC, which needs major hepatectomy. Such information will influence the evidence-based policy in professional practice in the management algorithm for HCC. Since postoperative complications and tumor recurrence are substantial after OMH, potential benefits of LMH tested in this study will help to alleviate these problems.
Detailed description
Background: Hepatocellular carcinoma (HCC) is the sixth most common malignancy in the world.The practice of screening by ultrasonography and serum alpha-fetoprotein concentration in cirrhotic patients and hepatitis B carriers has led to an increasing incidence of HCC.
Hepatectomy, local ablation and liver transplantation are regarded as the mainstay of curative treatment for HCC according to international guidelines by EASL, AASLD and ESMO.The shortage of liver grafts has limited the application of liver transplantation. Hepatectomy is thus widely accepted as the treatment option of choice for patients with HCC and non cirrhotic liver.
Major hepatectomy (resection of > 3 Couinaud's segments) is always needed when HCC is large or is close to major blood vessels within liver. With the advancements in techniques of hepatectomy and perioperative patient care, the operative mortality of open major hepatectomy (OMH) has reduced to < 5% in recent years. Nonetheless, OMH for HCC is still associated with major problems as follows:
- It is associated with significant morbidities. The morbidity rate after OMH remains high (30% - 40%) even in high-volume centres. Wound infection and bronchopneumonia are among the most common complications after hepatic resection. Long incision and vigorous retraction of the rib cage are required to achieve adequate exposure of the liver tumor during hepatic resection. As a result, sepsis due to chest complications and wound problems are frequently encountered. Furthermore, division of the porto-systemic collaterals in the anterior abdominal wall contributes to postoperative ascites, which is another common complication.
- It is associated with a high tumor recurrence rate, even when performed with a curative intent. The 3-year recurrence rate has been reported to be more than 50%. Most recurrences occur in the liver remnant, in the forms of intrahepatic metastasis or multicentric tumor recurrence. Risk factors related to recurrence include unfavorable tumor factors such as microscopic venous or capsular invasion. Hence, tumor cell dissemination could be the main mechanism of recurrence. In this context, manipulation of the tumor during OMH leading to tumor cell dissemination can potentially contribute to high tumor recurrence rate. Furthermore, it has been suggested that postoperative immunosuppression induced by surgical stress may induce tumor growth in the liver remnant.
Laparoscopy has a well-defined role in the staging and diagnosis of hepatobiliary malignancies. However, laparoscopic hepatectomy has not yet been widely practiced, because of the technical difficulties in liver resection, difficulty in the control of hemorrhage during liver transection and retraction of the liver for optimum exposure. With the advanced laparoscopic techniques, much enthusiasm has been developed in laparoscopic major hepatectomy (LMH). Recent series have proven the feasibility and safety of LMH for HCC. The selection criteria of the reported series included tumor size up to 10cm and single or multiple tumors confined to one liver lobe. The overall conversion rates was around 10%. There was no hospital mortality and the morbidity rate was about 10%. Apart from the documented advantages of laparoscopic surgery (less wound and chest complications, and shorter hospital stay), theoretically, LMH carries oncological advantages over OMH. LMH may result in less surgical stress and immunosuppression due to less intraoperative blood loss than OMH. Moreover, using laparoscopic instruments, it involves minimal manipulation of the tumor and less cancer cells dissemination during surgery. Potentially, postoperative tumor recurrence could be reduced and hence patient survival could be prolonged.
To date, only retrospective studies using propensity score matching to compare LMH with OMH were reported. In these study, the studied patient number was small (< 40) in each matched treatment arm and the reported 2-year overall (86% - 88% vs. 85% - 100%) and recurrence-free survival (72% - 83% vs. 81% - 85%) rates were comparable between OMH and LMH. Nevertheless, there is a trend that LMH is associated with better overall and recurrence-free survival than OMH. It is likely that these studies were underpowered (Type II error) to show the potential oncological benefits of LMH over OMH. Because of these limited data on LMH, according to EASL, AASLD and ESMO guidelines, its role for HCC is still not yet defined. In the sphere of laparoscopic hepatectomy, according to the European Guideline Meeting for Laparoscopic Liver Surgery (Southampton consensus), there was only limited data on short-term outcome but no data on long-term outcome of LMH. With these reasons, there is an urge for a prospective study aiming to define the role of LMH for HCC with respect to its potential oncological benefits.
In the principle investigator's institution (the Department of Surgery, The Chinese University of Hong Kong), preliminary data using propensity score matching analysis on patients with HCC (median size = 4cm) undergone either laparoscopic (n = 112) or open hepatectomy (n = 224) (major hepatectomy accounts for 40.5%), the intraoperative blood loss (median: 159 mL vs. 419 mL), blood transfusion rate (0% vs. 4.5%) and morbidity rate (5.4% vs. 28.1%) were significantly lower in laparoscopic group than open group. The hospital mortality (0% vs. 0.4%), long-term overall (5-year: 56% vs. 42%) and recurrence free (5-year: 36% vs. 33%) survival rates were comparable between groups. (Supplementary information attached) With this experience, the principle investigator proposes an open labelled prospective multi-center randomized trial (AP-LAPO Trial) comparing LMH with OMH for HCC. This study involves 5 high-volume centres specialized in liver surgery and with facilities supporting LMH and OMH in Asia-Pacific region (Hong Kong, Sichuan, Guangzhou and Foshan). These centres perform at least 30 LMH or OMH per year (The Chinese University of Hong Kong, median no. = 51; Kwong Wah Hospital, median no. = 30; West China Medical School of Sichuan University, median no. 120; Eastern Hepatobiliary Surgery Hospital \& Institute, median no. = 115; The First People's Hospital of Foshan, median no. = 102), and have achieved excellent perioperative and oncological outcome after LMH or OMH (operative mortality 1% - 2%; complication rate 14% - 23%; 2-year overall survival rate 85% - 88%; 2-year disease-free survival rate 81% - 84%).
Objectives and hypothesis: The primary objective is to test the hypothesis that LMH is associated with less surgical stress, less immunosuppression and thus less tumor recurrence and better survival than OMH. The primary outcome measure is 2-year recurrence-free survival. The secondary outcome measures include hospital mortality, morbidity, quality of life and overall survival between groups. Besides, stress-related cytokines (interleukin-6 [IL-6] and immunosuppressive acidic protein[IAP]) will also be measured during the perioperative
Sample size estimation: Based on a reported 2-year recurrence-free survival rate of 72% after OMH and an expected 88% after LMH (about 20% improvement) according to a previously reported series, 106 patients need to be recruited to each arm in order to demonstrate a statistically significant difference with a 80% power at the 0.05 level of 2-sided significant difference between laparoscopic and open hepatic resection, allowing a drop-out rate of 10%. This sample size will also allow detection of reduction of 2-year tumor recurrence from 50% in OMH group to 30% in LMH with a similar power and level of significance. The principle investigator's unit is a major referral center for management of HCC in Hong Kong, with more than 150 new cases seen per year. There are one other centers in Hong Kong and 3 centers in Mainland China, which are specialized in both laparoscopic and open surgery for patients with HCC, with referral patient number ranging from 50 to 200 per year. The planned number of patients recruited in each participating centres is as follows (The Chinese University of Hong Kong, N = 32; Kwong Wah Hospital, N = 20; West China Medical School of Sichuan University, N = 50; Eastern Hepatobiliary Surgery Hospital \& Institute, N = 50; The First People's Hospital of Foshan, median no. = 60) It is therefore expected that recruitment can be completed in about 12 months. All patients will be observed for at least 24 months after treatment. Hence, the total period of study including follow-up is estimated to be about 3 years for the funding period. After the funding period, recruited patients will be followed up periodically up to 5 years after surgery to evaluate the long-term outcome.
Statistical analysis: Statistical analysis will be performed using SPSS version 11.0 (SPSS Inc., Chicago, Ill). The 2-year recurrence-free survival (primary outcome) will be evaluated by Kaplan-Meier method and compared by the log-rank test between studied groups.
Other secondary outcome measures will be compared using Chi-squared test or Fisher's exact test for categorical variables, and Mann-Whitney U test for continuous variables between groups. Overall survival is again computed by the Kaplan-Meier method and compared by the log-rank test between groups. P < 0.05 is considered statistically significant.
Ethical consideration: All aspects of the study will be discussed with each subject during a phone interview or screening visit. An information sheet will be provided, and each subject will be given the opportunity to seek medical advice or to discuss the study with friends or family prior to involvement. Each volunteer will give written, informed consent, in accordance with the attached form, and the subjects will be free to withdraw from the study at any time. This study will be performed in accordance with the ethical standards of the Declaration of Helsinki of 1975 and its later versions. Ethics approval from the institutional review broad of individual center will be sought.
Relevance to clinical applications: The proposed study is an open-labelled prospective multi-center randomized trial investigating the potential benefits of laparoscopic major hepatectomy for hepatocellular carcinoma (HCC), as compared to conventional open surgery. It involves 5 high-volume surgery centers in the Asia-Pacific region, where the incidence of hepatocellular carcinoma is high. The result of this study provides level 1 evidence on the best treatment option for HCC, which needs major hepatectomy. Such information will influence the evidence-based policy in professional practice in the management algorithm for HCC. Since postoperative complications and tumor recurrence are substantial after OMH, potential benefits of LMH tested in this study will help to alleviate these problems. Ultimately, the long-term survival of patients with HCC could be improved.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Patients with hepatocellular carcinoma which undergone major hepatectomy will be randomized to either laparoscopic or open surgery group
| Arm | Type | Receives |
|---|---|---|
| Open major hepatectomy | Active comparator | Procedure: Open or laparoscopic surgeryResection of the tumor together with 3 or more liver segments using open standard techniques of hepatectomy |
| Laparoscopic major hepatectomy | Active comparator | Procedure: Open or laparoscopic surgeryResection of the tumor together with 3 or more liver segments using minimally invasive techniques of hepatectomy |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Diagnosis of HCC is in accordance to the diagnostic criteria for HCC used by the European Association for the Study of the Liver. HCC was diagnosed when the radiologic imaging techniques (spiral contrasted CT scan or contrasted MRI) showed typical features of HCC (contrast enhancement in the arterial phase and rapid wash-out of contrast in the venous or delayed phase) and/or elevated serum alpha fetoprotein (AFP) level.
- HCC of maximum diameter up to 10 cm; Single or multiple tumor nodules confined to one liver lobe according to the previous reported series
- Major hepatectomy (resection of > 3 Couinaud's segments) is required as judged by hepatobiliary surgeons
- Absence of extrahepatic metastasis or radiological evidence of venous invasion of major portal vein or hepatic vein branches
- Child's A liver function
Key exclusion criteria (3 listed)
- Tumors unfavorable for major hepatectomy (e.g. bilobar tumors, main portal vein tumor thrombus and/or inadequate future liver volume)
- Previous treatment for HCC (e.g. transarterial chemoembolization, or chemotherapy)
- Tumors require combined hepatectomy and thermal ablation therapy
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 |
|---|---|---|
| Open or laparoscopic surgeryPatients, with their consent, will be recruited to participate by investigators after considering the inclusion and exclusion criteria. Treatment allocation to the eligible patients will follow a randomization schedule. A total of 212 subjects will be randomized 1:1 to one of the two treatment arms: 1. Laparoscopic group: LMH 2. Open group: OMH | Procedure or surgery | Laparoscopic major hepatectomy, Open major hepatectomy |
Primary outcome
2-year recurrence-free survival
Time frame: 2 years
The proportion of patients surviving without tumor recurrence as measured by postoperative images (CT or MRI) at 2 years
4 secondary outcomes
Hospital mortality
Time frame: 1 year
Morbidity
Time frame: 1 year
Quality of llife
Time frame: 1 year
5 - year Overall survival
Time frame: 5 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2023.
- Background: PubMed 30207593Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
- Background: PubMed 29628281European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J Hepatol. 2018 Jul;69(1):182-236. doi: 10.1016/j.jhep.2018.03.019. Epub 2018 Apr 5. No abstract available.
- Background: PubMed 28130846Heimbach JK, Kulik LM, Finn RS, Sirlin CB, Abecassis MM, Roberts LR, Zhu AX, Murad MH, Marrero JA. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology. 2018 Jan;67(1):358-380. doi: 10.1002/hep.29086. No abstract available.
- Background: PubMed 30285213Vogel A, Cervantes A, Chau I, Daniele B, Llovet JM, Meyer T, Nault JC, Neumann U, Ricke J, Sangro B, Schirmacher P, Verslype C, Zech CJ, Arnold D, Martinelli E; ESMO Guidelines Committee. Hepatocellular carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018 Oct 1;29(Suppl 4):iv238-iv255. doi: 10.1093/annonc/mdy308. No abstract available.
- Background: PubMed 15915370Ng KK, Vauthey JN, Pawlik TM, Lauwers GY, Regimbeau JM, Belghiti J, Ikai I, Yamaoka Y, Curley SA, Nagorney DM, Ng IO, Fan ST, Poon RT; International Cooperative Study Group on Hepatocellular Carcinoma. Is hepatic resection for large or multinodular hepatocellular carcinoma justified? Results from a multi-institutional database. Ann Surg Oncol. 2005 May;12(5):364-73. doi: 10.1245/ASO.2005.06.004. Epub 2005 Mar 31.
- Background: PubMed 27632953Hao S, Fan P, Chen S, Tu C, Wan C. Anterior approach to improve the long-term outcome in patients with large-size hepatocellular carcinoma having liver resection. J Surg Oncol. 2016 Dec;114(7):872-878. doi: 10.1002/jso.24433. Epub 2016 Sep 16.
- Background: PubMed 22828986Lee KF, Cheung YS, Wong J, Chong CC, Wong JS, Lai PB. Randomized clinical trial of open hepatectomy with or without intermittent Pringle manoeuvre. Br J Surg. 2012 Sep;99(9):1203-9. doi: 10.1002/bjs.8863. Epub 2012 Jul 24.
- Background: PubMed 29091283Ng KKC, Chok KSH, Chan ACY, Cheung TT, Wong TCL, Fung JYY, Yuen J, Poon RTP, Fan ST, Lo CM. Randomized clinical trial of hepatic resection versus radiofrequency ablation for early-stage hepatocellular carcinoma. Br J Surg. 2017 Dec;104(13):1775-1784. doi: 10.1002/bjs.10677. Epub 2017 Nov 1.
- Background: PubMed 31500787Ng KK, Cheung TT, Pang HH, Wong TC, Dai JW, Ma KW, She WH, Kotewall CN, Lo CM. A simplified prediction model for early intrahepatic recurrence after hepatectomy for patients with unilobar hepatocellular carcinoma without macroscopic vascular invasion: An implication for adjuvant therapy and postoperative surveillance. Surg Oncol. 2019 Sep;30:6-12. doi: 10.1016/j.suronc.2019.05.017. Epub 2019 May 22.
- Background: PubMed 10767798Jarnagin WR, Delman K, Kooby D, Mastorides S, Zager J, Brennan MF, Blumgart LH, Federoff H, Fong Y. Neoadjuvant interleukin-12 immunogene therapy protects against cancer recurrence after liver resection in an animal model. Ann Surg. 2000 May;231(5):762-71. doi: 10.1097/00000658-200005000-00017.
- Background: PubMed 29737513Halls MC, Berardi G, Cipriani F, Barkhatov L, Lainas P, Harris S, D'Hondt M, Rotellar F, Dagher I, Aldrighetti L, Troisi RI, Edwin B, Abu Hilal M. Development and validation of a difficulty score to predict intraoperative complications during laparoscopic liver resection. Br J Surg. 2018 Aug;105(9):1182-1191. doi: 10.1002/bjs.10821. Epub 2018 May 8.
- Background: PubMed 30180140Chen K, Pan Y, Hu GY, Maher H, Zheng XY, Yan JF. Laparoscopic Versus Open Major Hepatectomy for Hepatocellular Carcinoma: A Meta-Analysis. Surg Laparosc Endosc Percutan Tech. 2018 Oct;28(5):267-274. doi: 10.1097/SLE.0000000000000567.
- 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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Open or laparoscopic surgery 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 8 inclusion and 3 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: status not confirmed, 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Kelvin.K.C Ng, MS, PhD (+852 9124 2695, kelvinng@surgery.cuhk.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
2-year recurrence-free survival (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04852211, which also lists 30 linked publications.
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.