Laparoscopic versus open left hemihepatectomy for hepatocellular carcinoma: a propensity score matching analysis
Original Article

Laparoscopic versus open left hemihepatectomy for hepatocellular carcinoma: a propensity score matching analysis

Yong Yi1,2#, Jialei Weng1,2#, Chenhao Zhou1,2#, Gao Liu1,2, Ning Ren1,2,3

1Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China; 2Key Laboratory of Carcinogenesis and Cancer Invasion of Ministry of Education, Shanghai, China; 3Institute of Fudan Minhang Academic Health System, and Key Laboratory of Whole-period Monitoring and Precise Intervention of Digestive Cancer (SMHC), Minhang Hospital & AHS, Fudan University, Shanghai, China

Contributions: (I) Conception and design: N Ren; Y Yi; (II) Administrative support: N Ren; (III) Provision of study materials or patients: Y Yi; C Zhou; (IV) Collection and assembly of data: J Weng; G Liu; (V) Data analysis and interpretation: J Weng; C Zhou; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

#These authors contributed equally to this work.

Correspondence to: Ning Ren. Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, 180 Fenglin Road, Xuhui District, Shanghai 200032, China. Email: ren.ning@zs-hospital.sh.cn.

Background: Despite the increasing application of laparoscopic hepatectomy (LH) for hepatocellular carcinoma (HCC), laparoscopic left hemihepatectomy (LLH) remains a relatively rare surgery and comparison of perioperative and oncological outcomes between LLH and open left hemihepatectomy (OLH) is lacking.

Methods: A total of 276 HCC patients who underwent either LLH or OLH between January 2008 and November 2019 were enrolled in this retrospective observational study and a 1:2 propensity score matching (PSM) was performed between LLH and OLH groups.

Results: Patients in LLH group had smaller tumor size (P=0.001) and earlier TNM staging (P=0.022) before matching. Despite the similar transfusion rate after matching, patients undergoing LLH (n=27) experienced less intraoperative blood loss (100.0 versus 200.0 mL; P=0.034) and application of hepatic portal occlusion (11.1% versus 63.5%; P<0.001) compared to those in OLH group (n=52). There were no statistical differences of resection margin and incidence of complications between the groups. The overall survival (OS) and disease-free survival (DFS) of patients in LLH group were comparable to OLH group (3-year OS rate: 75.0% versus 84.9%; 1-year DFS rate: 92.3% versus 92.2%).

Conclusions: LLH may be a feasible and safe alternative to OLH for selected HCC cases, providing potential short-term benefits without compromising oncologic adequacy and prognosis.

Keywords: Laparoscopic left hemihepatectomy (LLH); hepatocellular carcinoma (HCC); perioperative outcomes


Submitted Mar 18, 2020. Accepted for publication Aug 07, 2020.

doi: 10.21037/tcr-20-1573


Introduction

With the development of instruments, innovation of technology and accumulation of experience, past decades have seen an evolution of laparoscopic hepatectomy (LH) in hepatocellular carcinoma (HCC) treatment from local resection towards segmentectomy and even hemihepatectomy. Furthermore, increasing evidence has indicated the technical feasibility and operation safety of LH in HCC, as well as better perioperative benefits in comparison with conventional laparotomy (1-10). Although there is a trend of LH to replace open liver resection in some experienced institutes (11), the long-term survival benefit of LH is lack of sufficient supports and thus more follow-up studies and randomized controlled trials (RCT) are warranted.

HCC is the sixth most common cancer and the fourth leading cause of cancer death worldwide (12). Liver resection is considered as one of the most effective treatments for HCC (13,14). With the development of minimally invasive surgery, laparoscopic left lateral segmentectomy has also been regarded as the standard procedure and performed routinely in HCC (15). However, laparoscopic hemihepatectomy remains a relatively rare surgery because of rigorous technical demands, complicated operational procedures and potentially huge risk. In this case, there are only a few studies reporting the superior outcomes like less intraoperative blood loss and postoperative complications of laparoscopic hemihepatectomy compared to open approach (16-18). However, these studies, with a small cohort of patients recruited, either focus on right hepatectomy or fail to adopt matching design. Given that major hepatectomy is an optimal choice for HCC patients with large tumors or better liver function reserve (18), it is imperative to further authenticate the feasibility, safety and real survival benefits of laparoscopic hemihepatectomy, especially left hepatectomy, in HCC.

Hence, in this study, we aimed to compare the perioperative and long-term outcomes of laparoscopic left hepatectomy (LLH) and open left hepatectomy (OLH) in HCC. We present the following article in accordance with the STROBE reporting checklist (available at http://dx.doi.org/10.21037/tcr-20-1573).


Methods

Patients and data

This is a retrospective observational study with a matching analysis. A total of 276 patients who received left hemihepatectomy for HCC with either a laparoscopic or an open approach at Zhongshan Hospital of Fudan University, Shanghai, China between January 2008 and November 2019 were included. The inclusion and exclusion criteria of patients were as following: (I) All patients underwent primary curative LLH or OLH; (II) clinical diagnosis of HCC was confirmed by postoperative pathology; (III) no history of other malignancy; (IV) with Child-Pugh class A or early B liver function; (V) no evidence of extra-hepatic metastasis or portal vein or inferior vena cava cancer embolus; (VI) open conversion cases were excluded; (VII) emergency operation due to tumor rupture was also excluded. LLH and OLH were performed by the same team of professional liver surgeons and selection of surgical approach was surgeon dependent. Among these patients, 35 individuals underwent LLH and other 241 patients were operated with OLH. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). A written informed consent for operation was obtained from each patient and this study was approved by the Clinical Research Ethics Committee of Zhongshan Hospital, Fudan University (ID: Y2018-115).

Demographic characteristics, preoperative imaging and laboratory, operative record, and pathologic report of all patients were collected from electrical medical record system. Postoperative complications were graded according to the Clavien-Dindo classification (19). Postoperative follow-up, mainly encompassing abdominal ultrasound and serological tumor biomarkers, was conducted every 3 months. Recurrence was confirmed by enhanced computed tomography (CT) or magnetic resonance imaging (MRI). The interval between the time of surgery and the date of either death or the last follow-up time was considered as overall survival (OS). Disease-free survival (DFS) was defined as the time from the date of operation to the point of the recurrence during the follow-up period. For patients without recurrence, DFS was censored on the date of death or the last follow-up time.

Propensity score matching (PSM)

To minimize selection bias in this nonrandomized observational study, PSM analysis was employed to balance the distribution of covariates between two groups (20). The following variables were considered seriously and finally enrolled into PSM model: age, gender, alpha-fetoprotein (AFP) level, Tumor Node Metastasis (TNM) staging, presence of cirrhosis or ascites, tumor size and differentiation, and micro-vascular invasion (MVI). A propensity score of each variable was calculated by logistic regression and a 1:2 ratio matching between LLH and OLH groups was achieved by nearest neighbor method. PSM analysis was performed by the “MatchIt” package of R software (version 3.6.1).

Surgical procedure

In an LLH, the patient lay in the French position under general anesthesia. Pneumoperitoneum was established after the insertion of a 12-mm port into a supraumbilical cutdown and was maintained at around 15 mmHg. Generally, four working ports were applied as follows: three 5-mm ports in the right upper, left upper and right flank quadrants and a 10-mm port in the left flank quadrant.

First, the hepatic artery and the portal vein were well exposed by meticulous blunt dissection. The left branches of these two main vessels were then clamped with absorbable clips to achieve selective left inflow occlusion. Left hepatic parenchymal transection was performed using a Harmonic scalpel and hemostasis was conducted by hem-o-lock clips and bipolar electrocoagulation. Finally, after ligation of left hepatic vein, the specimen was put into a plastic bag and retrieved through an extended abdominal incision.

In an OLH, the patient was placed in the supine position and a subcostal incision was performed routinely. The procedures of surgery were similar to LLH. Briefly, parenchymal transection was performed after occlusion of left hepatic artery and left portal vein. Fibrin glue was also applied to ensure the hemostasis. An abdominal drainage tube was placed after LLH or OLH.

Statistical analysis

Data was expressed as mean ± standard deviation (SD), median with range or count with percentage. Statistical analyses were performed by SPSS software (22.0; IBM, Armonk, NY, USA). Student’s t-test or Mann-Whitney U test was chosen based on the data distribution for comparison of continuous variables. Pearson Chi-square test and Fisher’s exact test were employed to compare discrete variables. The survival curves of OS and DFS were plotted using Kaplan-Meier method and difference of survival between LLH and OLH group was tested by log-rank test. A two-tailed P value <0.05 was considered as statistical significance.


Results

Baseline and pathologic characteristics

A total of 276 patients were enrolled in the study with 35 individuals in LLH group and 241 in OLH group. As listed in Table 1, there were significant differences of several baseline characteristics between the two groups such as previous abdominal surgery (P=0.043), albumin (P<0.001), prothrombin time (PT) (P=0.024) and AFP (P=0.009). Other demographic variables, like age, gender, comorbidity, hepatitis, other laboratory indexes, hepatitis B virus (HBV), and ascites did not meet the statistical significance. PSM analysis was then performed and well-balanced baseline characteristics except albumin (P=0.015) between LLH (n=27) and OLH (n=52) groups were observed after matching. Similarly, LLH and OLH groups differed before PSM in terms of tumor size (P=0.001), cell differentiation (P=0.020), MVI (P=0.001), and TNM staging (P=0.022) (Table 2). Subsequent matching successfully eliminated the statistical difference of these pathological features between the two groups. No significant difference was found in tumor number, tumor border, tumor encapsulation, tumor necrosis and hemorrhage, and liver cirrhosis before and after PSM.

Table 1

Comparison of baseline characteristics between LLH and OLH groups before and after PSM

Characteristics Before matching After matching
LLH (n=35) OLH (n=241) P LLH (n=27) OLH (n=52) P
Age (years) 56.3±14.2 56.2±11.8 0.967* 58.0±12.1 57.4±10.8 0.824*
Gender, n (%) 0.436 0.366
   Male 27 (77.1) 199 (82.6) 20 (74.1) 43 (82.7)
   Female 8 (22.9) 42 (17.4) 7 (25.9) 9 (17.3)
Comorbidity, n (%) 0.281 0.146
   Hypertension 9 (25.7) 42 (17.4) 6 (22.2) 9 (17.3)
   Diabetes 6 (17.1) 18 (7.5) 5 (18.5) 3 (5.8)
   CVA 0 (0.0) 6 (2.5) 0 (0.0) 3 (5.8)
   CD 1 (2.9) 7 (2.9) 0 (0.0) 3 (5.8)
Hepatitis, n (%) 23 (65.7) 158 (65.6) 0.986 17 (63.0) 30 (57.7) 0.651
PAS, n (%) 10 (28.6) 36 (14.9) 0.043 7 (25.9) 6 (11.5) 0.188
Laboratory index
   TB (μmol/L) 11.5 (5.2–34.7) 11.2 (3.8–192.0) 0.684 11.5 (5.2–29.9) 10.2 (4.9–38.3) 0.249
   DB (μmol/L) 4.0 (1.1–8.6) 4.4 (0.2–90.1) 0.302 4.0 (1.1–8.6) 4.4 (1.9–16.4) 0.377
   Albumin (g/L) 44.0 (34.0–58.0) 41.0 (21.0–50.0) <0.001 44.0 (34.0–49.0) 41.0 (30.0–50.0) 0.015
   ALT (U/L) 27.0 (8.0–86.0) 31.0 (6.0–625.0) 0.303 29.0 (8.0–86.0) 29.0 (9.0–625.0) 0.934
   AST (U/L) 27.0 (16.0–50.0) 31.0 (12.0–656.0) 0.152 27.0 (16.0–50.0) 28.5 (15.0–656.0) 0.860
   Hb (g/L) 145.5±16.3 141.0±15.3 0.105* 147.4±14.9 140.7±16.6 0.086*
   WBC (109/L) 5.09 (2.64–12.39) 5.70 (2.16–15.87) 0.197 5.14 (2.64–12.39) 5.55 (2.73–9.28) 0.840
   Platelet (109/L) 159.0 (92.0–277.0) 170.0 (45.0–542.0) 0.530 160.0 (92.0–262.0) 167.0 (45.0–542.0) 0.996
   PT (s) 11.5 (9.9–12.7) 11.7 (9.4–19.2) 0.024 11.5 (9.9–12.7) 11.5 (9.4–14.3) 0.511
   AFP (ng/mL) 10.0 (1.0–1,717.0) 59.2 (1.0–60,500.0) 0.009 8.5 (1.0–1717.0) 10.5 (1.0–1,580.0) 0.804
HBV (+), n (%) 28 (80.0) 183 (75.9) 0.596 21 (77.8) 42 (80.8) 0.754
Ascites, n (%) 0 (0.0) 7 (2.9) 0.601† 0 (0.0) 2 (3.8) 0.544

*, Student’s t-test; , Fisher’s exact test. AFP, indicates alpha-fetoprotein; ALT, alanine transaminase; AST, aspartate transaminase; CD, coronary disease; CVA, cerebrovascular accident; DB, direct bilirubin; Hb, hemoglobin; HBV, hepatitis B virus; LLH, laparoscopic left hemihepatectomy; OLH, open left hemihepatectomy; PAS, previous abdominal surgery; PSM, propensity score matching; PT, prothrombin time; TB, total bilirubin; WBC, white blood cells.

Table 2

Comparison of pathologic characteristics between LLH and OLH groups before and after PSM

Characteristics Before matching After matching
LLH (n=35) OLH (n=241) P LLH (n=27) OLH (n=52) P
Tumor size (cm) 5.2±2.2 6.7±3.8 0.001* 5.1±2.3 5.3±2.9 0.785*
Tumor number, n (%) 1.000 0.114
   Solitary 33 (94.3) 224 (92.9) 25 (92.6) 52 (100.0)
   Multiple 2 (5.7) 17 (7.1) 2 (7.4) 0 (0.0)
Tumor border, n (%) 0.155 0.514
   Clear 35 (100.0) 221 (91.7) 27 (100.0) 49 (94.2)
   Unclear 0 (0.0) 20 (8.3) 0 (0.0) 3 (5.8)
Encapsulation, n (%) 0.115 0.246
   Complete 28 (80.0) 152 (63.1) 23 (85.2) 37 (71.2)
   Incomplete 2 (5.7) 14 (5.8) 1 (3.7) 1 (1.9)
   None 5 (14.3) 75 (31.1) 3 (11.1) 14 (26.9)
Differentiation, n (%) 0.020 0.659
   Grade I 1 (2.9) 9 (3.7) 1 (3.7) 4 (7.7)
   Grade II 21 (60.0) 194 (80.5) 19 (70.4) 38 (73.1)
   Grade III 13 (37.1) 37 (15.4) 7 (25.9) 10 (19.2)
   Grade IV 0 (0.0) 1 (0.4) 0 (0.0) 0 (0.0)
Tumor necrosis, n (%) 8 (22.9) 61 (25.3) 0.754 5 (18.5) 13 (25.0) 0.515
Tumor hemorrhage, n (%) 1 (2.9) 2 (0.8) 0.335 1 (3.7) 0 (0.0) 0.342
Micro-vascular invasion, n (%) 14 (40.0) 39 (16.2) 0.001 6 (22.2) 15 (28.8) 0.527
TNM staging, n (%) 0.022 0.438
   I 26 (74.3) 111 (46.1) 18 (66.7) 30 (57.7)
   II 9 (25.7) 112 (46.5) 9 (33.3) 22 (42.3)
   IIIA 0 (0.0) 11 (4.5) 0 (0.0) 0 (0.0)
   IIIB 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
   IIIC 0 (0.0) 7 (2.9) 0 (0.0) 0 (0.0)
Cirrhosis, n (%) 24 (68.6) 159 (66.0) 0.761 18 (66.7) 34 (65.4) 0.909

*, Student’s t-test; , Fisher’s exact test. LLH, indicates laparoscopic left hemihepatectomy; OLH, open left hemihepatectomy; PSM, propensity score matching; TNM, Tumor Node Metastasis.

Difference of surgical outcomes between LLH and OLH groups after PSM

We further retrospectively compared the surgery details between LLH and OLH groups after PSM. As shown in Table 3, the median intraoperative blood loss was significantly less in LLH group compared to OLH group (100.0 versus 200.0 mL; P=0.034). There was no significant difference between the two groups regarding the transfusion rate (0.0% versus 3.8%; P=0.544). In addition, the rate of hepatic portal occlusion in LLH group was significantly lower than OLH group (11.1% versus 63.5%; P<0.001). Resection margin, determined by pathology, was defined as the closest distance of surgical margin to tumor. It showed that the mean resection margin was comparable between the groups (1.2 versus 1.0 cm; P=0.597). None of the patients in LLH group developed complications greater than Clavien-Dindo classification II, while there was atrial fibrillation (n=1), infection (n=2), delirium (n=1), jaundice (n=1), and the need for blood transfusion (n=1) or thoracentesis (n=1) in OLH group (P=0.116).

Table 3

Comparison of surgical outcomes between LLH and OLH groups after PSM

Outcomes LLH (n=27) OLH (n=52) P
Blood loss (mL) 100.0 (10.0–800.0) 200.0 (10.0–1,000.0) 0.034
Blood transfusion, n (%) 0 (0.0) 2 (3.8) 0.544
Hepatic portal occlusion 3 (11.1) 33 (63.5) <0.001
Resection margin (cm) 1.2±1.0 1.0±0.7 0.597
Clavien-Dindo grade, n (%) 0.116
   I 27 (100.0) 45 (86.6)
   II 0 (0.0) 6 (11.5)
   IIIa 0 (0.0) 1 (1.9)

, Fisher’s exact test. LLH, indicates laparoscopic left hemihepatectomy; OLH, open left hemihepatectomy; PSM, propensity score matching.

Difference of long-term survival between LLH and OLH groups after PSM

The median follow-up was 12.40 months (range, 1.43 to 46.40 months) in LLH group and 32.78 months (range, 9.77 to 128.80 months) in OLH group. HCC recurrences were observed in four patients undergoing LLH and 12 patients in OLH group. One patient (3.70%) in LLH group and three patients (5.77%) in OLH group succumbed to tumor recurrence or metastasis. The OS and DFS of patients receiving LLH were comparable to those in OLH group (P=0.8401; P=0.3655, respectively) (Figure 1).

Figure 1 Kaplan-Meier overall survival (OS) (A) and disease-free survival (DFS) (B) curves of HCC patients in LLH and OLH group. Survival difference was analyzed using log-rank test. LLH, laparoscopic left hemihepatectomy; OLH, open left hemihepatectomy.

Discussion

Since the first report of laparoscopic liver resection by Reich et al. in 1991 (21), past decades have witnessed the increasing application of laparoscopic surgery in liver disease, including HCC. After the course of technique innovation and procedure exploration in the first 10 years of 21st century, recent attentions have been focused on evaluation of the performance of laparoscopic liver resection over conventional laparotomy (11). Several advantages of laparoscopic minor hepatic resection, sectionectomy, and segmentectomy over open approach, like less intraoperative blood loss (1,5,22-26), shorter postoperative hospital stay (1,5,22-28), have been widely reported by surgeons. Nevertheless, there is no strong evidence like RCT supporting these conclusions and replacement of open liver resection by LH is still challenging.

An important challenge is to achieve anatomical resection of HCC through laparoscopy. Anatomic resection, such as major hepatectomy and hemihepatectomy, is preferred considering the malignancy of the disease and the intention of curative resection (29). Some studies have indicated that laparoscopic anatomic hepatectomy is feasible in selected patients with the premise of rich experience, committed practice and proper coaching (30,31). However, this technology is limited to a few advanced medical centers because of the technically demanding procedure and thus relevant studies are lacking.

Here, this study enrolled 276 patients who received left hemihepatectomy for HCC in our hospital. We noticed that some patients undergoing LLH had cirrhosis or a tumor size larger than 5 cm. Cirrhosis can increases the risk of intraoperative bleeding and postoperative liver failure (32). The successful operation for these patients suggests that the presence of cirrhosis or large tumor may be not a limiting factor or contraindication for LLH. In addition, it is imperative to perform a PSM analysis in this observational study as we found that patients in LLH group tended to have smaller tumor size (P=0.001) and earlier TNM staging (P=0.022). This may reflect the preference of surgeons in selecting patients for LLH. As we wished, the different distributions of covariates between LLH and OLH groups, especially like AFP, tumor size, cell differentiation, MVI, and TNM staging, were well balanced after PSM.

There was a tendency of less intraoperative blood loss and lower hepatic portal occlusion rate in patients undergoing LLH in comparison with those in OLH group. Besides, we found that the transfusion rate was not significantly different between the two groups after matching. Similar results were reported in previous studies on anatomic hepatectomy (17,18,29). The control of bleeding is an important part of surgery and thus sometimes hepatic inflow occlusion like Pringle maneuver is necessary during the parenchymal transection. During the operation of LLH, our team generally use the Glissonean pedicle approach of left hepatic artery and portal vein for inflow control, which can reduce the incidence of ischemia-reperfusion injury and gastrointestinal congestion. At the same time, ultrasound and intraoperative indocyanine green-fluorescence imaging technique are used for identification of the Glissonean system and margin of liver segments, respectively. For parenchymal transection, ultrasonic dissection and stapler are most commonly used and the middle hepatic vein should be exposed on the cutting plane for better blood control. In case of uncontrollable bleeding, conversion to the open surgery should be performed without hesitation. These experiences in LLH help us effectively control intraoperative blood loss. The reduction of bleeding in LLH is believed to be derived from some additional advantages of laparoscopy. For example, the establishment of pneumoperitoneum could lead to a lower central venous pressure (1,23) and the magnification of laparoscopy allows for a more meticulous dissection of liver parenchyma (1). The less application of hepatic portal occlusion in LLH group indicated a decreased risk of liver ischemia-reperfusion injury and dysfunction during the laparoscopic surgery.

Resection margin is an important factor that could influence long-term survival (23). Although it was initially considered that LH would compromise the resection margin due to the lack of palpation (29), the magnification of laparoscopy, the anatomical resection, and the routine application of laparoscopic ultrasound may compensate the deficiency of palpation. In this study, consistent with other researches (7,24,25,28,29), no significant difference in surgical margin was observed between the two groups.

The frequency and severity of postoperative complications are considered as important evaluations of surgical quality. Although the rate of complications (Clavien-Dindo classification II or above) in LLH group was lower than that in OLH group (0.0% versus 13.3%), no statistical difference was presented in this study. However, another study reported a significantly lower postoperative morbidity of LLH group (17). Different results may be attributed to the small cohorts of patients and variances in surgical operations across teams in different studies.

Finally, we found that patients in LLH group experienced comparable OS and DFS to those in the OLH group. The long-term postoperative prognosis is the major controversy of LH for HCC treatment (11). According to the results of our and other studies (18,33,34), the surgical method appears not to have an obvious influence on oncological outcomes of HCC patients. It may be partially explained by the similar surgical details like resection margin and rate of complications between LLH and OLH groups. Nevertheless, more supportive evidence is warranted to get the final conclusion.

There are some limitations in this study. First, the design of retrospective observation in a single surgical center makes it necessary to conduct prospective, multicenter studies in the future. Nevertheless, the operation of LLH is generally restricted to specific tertiary hospitals, which makes the external validation of our study findings challenging. Second, due to the complicated procedures and a steep learning curve, the number of patients undergoing LLH is limited. The small sample size has an adverse impact on statistical reliability and validity, which may affect the validity of our findings like the incidence of postoperative complications mentioned earlier. Though PSM analysis is performed to reduce selection bias as much as possible, results of study with a large cohort of patients will be more convincing. Third, the follow-up period should be longer.


Conclusions

In conclusion, this study is valuable in view that research on the application of LLH for HCC patients is relatively lacking. Despite the limited sample size and need for further research, the current study demonstrates the potential benefit of LLH on short-term outcomes of HCC patients without compromising the oncological prognosis. LLH may be a feasible and safe alternative to OLH for selected HCC patients, even in those with cirrhosis and large tumors.


Acknowledgments

Funding: This work was supported by the Shanghai International Science and Technology Collaboration Program (18410721900), the Shanghai Science and Innovation Action Plan Program (19511121304), the National Natural Science Foundation of China (81472672).


Footnote

Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/tcr-20-1573

Data Sharing Statement: Available at http://dx.doi.org/10.21037/tcr-20-1573

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr-20-1573). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). A written informed consent for operation was obtained from each patient and this study was approved by the Clinical Research Ethics Committee of Zhongshan Hospital, Fudan University (ID: Y2018-115).

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Yi Y, Weng J, Zhou C, Liu G, Ren N. Laparoscopic versus open left hemihepatectomy for hepatocellular carcinoma: a propensity score matching analysis. Transl Cancer Res 2020;9(9):5484-5492. doi: 10.21037/tcr-20-1573

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