McKeown or Ivor Lewis minimally invasive esophagectomy: a systematic review and meta-analysis
Original Article

McKeown or Ivor Lewis minimally invasive esophagectomy: a systematic review and meta-analysis

Jingpu Wang1, Jingfeng Hu1, Dengyan Zhu1, Kankan Wang2, Chunzhi Gao3, Tingting Shan1, Yang Yang1

1Department of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, China; 2Department of Nephrology, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, China; 3Department of Spinal Orthopedics, General Hospital of Pingmei Shenma Medical Group, Pingdingshan 467000, China

Contributions: (I) Conception and design: J Wang; (II) Administrative support: Y Yang, D Zhu; (III) Provision of study materials or patients: J Wang, J Hu, T Shan; (IV) Collection and assembly of data: J Wang, J Hu; (V) Data analysis and interpretation: K Wang, C Gao; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Yang Yang, PhD. The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, No.1 East Jianshe Road, Zhengzhou 450052, China. Email: fccyangy1@zzu.edu.cn.

Background: Minimally invasive esophagectomy (MIE) is increasingly accepted in many countries. McKeown esophagectomy and Ivor Lewis esophagectomy are two protocols commonly used for MIE, but which one provides more benefit to the patients remains matter of controversy.

Methods: All records in PubMed, Embase, Medline, The Cochrane Library, Wanfang Database, China National Knowledge Infrastructure (CNKI) and Chinese VIP Information till May 2019 were systematically retrieved to compare the cohort studies of McKeown esophagectomy and Ivor Lewis esophagectomy. A meta-analysis of the extracted data was performed using the Review Manager 5.3 and Stata 15 software.

Results: The meta-analysis included 23 cohort studies in which a total of 4,933 patients were enrolled. The results revealed that minimally invasive McKeown esophagectomy (MIME) was superior to minimally invasive Ivor Lewis esophagectomy (MILE) in hospital cost, but inferior to it in operating time, length of hospital stay, in-hospital mortality, 30-day mortality, 90-day mortality, anastomotic leakage, anastomotic leakage requiring surgery, anastomotic stenosis, recurrent laryngeal nerve (RLN) injury, chylothorax, pulmonary complications and total complications. There were no statistical differences between MIME and MILE in blood loss, detected number of lymph nodes, blood transfusion rate, R0 resection rate, re-operation rate, drainage duration, length of the stay in intensive care unit (ICU), 1-year mortality, lung infection, cardiac arrhythmia and delayed gastric emptying.

Conclusions: Except for the cost, MILE is superior to MIME in several aspects, and may represent a better choice for MIE. The results of the present study should be interpreted with caution since the meta-analysis is based on nonrandom cohort studies which may have a selection bias.

Keywords: Minimally invasive esophagectomy (MIE); Ivor Lewis esophagectomy; McKeown esophagectomy; cervical anastomosis; intrathoracic anastomosis


Submitted Sep 26, 2019. Accepted for publication Jan 06, 2020.

doi: 10.21037/tcr.2020.01.45


Introduction

Esophageal cancer is one of the most common cancers worldwide, with the highest incidence in the middle- and low-income countries (1). Esophageal cancer related mortality continues to increase (2), and in 2016 there were approximately 455,800 cases of this tumor and 400,200 deaths (1). Although considerable progress has been made in the diagnosis and treatment of esophageal cancer, globally, the overall 5-year survival rate is only 15–20% (3). Currently, esophageal resection and systematic lymph node dissection regarded as the best treatment methods for this type of cancer (4).

With the development of minimally invasive techniques and related devices, a growing body of evidence indicates that minimally invasive esophagectomy (MIE) has clear advantages over open esophagectomy. It is being increasingly accepted in many countries and has become the standard method for esophageal resection (5). Transhiatal esophagectomy, McKeown esophagectomy and Ivor Lewis esophagectomy are the top three procedures for MIE (6). Minimally invasive McKeown esophagectomy (MIME) and minimally invasive Ivor Lewis esophagectomy (MILE) are becoming more frequently utilized by surgeons since they allow a more thorough dissection of the thoracic lymph node (7). However, whether MIME of MILE has more clinical advantages and should become the recommended procedure remains a matter of controversy (8).

To identify the differences in short-term outcomes between the two procedures, meta-analyses have been conducted using intraoperative data, primary postoperative complications, and short-term mortality. Despite the high value of this research and the inclusion of several Chinese studies, data available from Chinese databases were not utilized. This is an important omission since according to World Health Organization, there were 572,034 new cases of esophageal cancer worldwide in 2018 and 307,359 of them were in China, accounting for 53.73% of global incidence. Therefore, it is critical to include the Chinese database in the meta-analysis. Additionally, the secondary endpoints considered in the previous studies have their limitations and the differences between two surgical procedures were not analyzed in a comprehensive way.

This report presents a systematic review and meta-analyses of the outcomes of MIME and MILE, utilizing both Chinese and English-language databases. The inclusion of the Chinese database allowed collecting a greater abundance of research data, resulting in a more comprehensive evaluation of the differences between the two surgical procedures.


Methods

This meta-analysis adheres to the requirements of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The systematic review and meta-analysis have been registered in the PROSPERO database (registration number: CRD42019128884). An IRB approval and informed consent of the patients were not required for this systematic review.

Literature search strategy

All results pertinent to the use of MIME and MILE available from PubMed, Embase, Medline, The Cochrane Library, Wanfang Database, China National Knowledge Infrastructure (CNKI), and Chinese VIP Information, deposited on or before May 2019, were retrieved using the search strategies designed by the authors (Supplementary file 1). Only studies published in Chinese and English were included, regardless of the language of the country where the study was performed. To ensure that the retrieval is as comprehensive as possible, and to reduce the selection bias, all references listed in the included studies were retrieved and analyzed manually.

Study selection

The literature retrieval was carried out independently by two assessors (J Wang and J Hu) and the cohort studies that did not fulfill the inclusion criteria were screened out. First, studies that based on the title and the abstract were evidently unrelated to MIME or MILE were disregarded. Subsequently, the considered studies were downloaded in full-text format and assessed according to inclusion criteria. Inclusion criteria were as follows: (I) research type: cohort studies (including prospective cohort studies and retrospective cohort studies); (II) surgical procedures: clear description of the surgical procedures, ensuring that the surgical protocol complied with the criteria of minimally invasive surgery; and (II) research results: presence of the data on anastomotic leakage. Any disagreement during the retrieval and screening process was discussed with and resolved by the third assessor (Y Yang).

Data extraction

The data were extracted and exchanged for examination by two assessors (J Wang and J Hu) independently. Any disagreement was discussed with and resolved by the third assessor (Y Yang). The extracted information included: (I) paper information: name of the first author, publication year, duration of the study, study design, and country; (II) patient information: number of enrolled patients, age, gender, and tumor site; and (III) the outcome parameters. The primary outcome parameter was the occurrence of an anastomotic leakage, while secondary outcome parameters included operating time, blood loss, number of lymph nodes obtained, R0 resection rate, drainage duration, re-operation rate, blood transfusion rate, length of stay in intensive care unit (ICU), length of hospital stay, cost, in-hospital mortality, 30-day mortality, 90-day mortality, 1-year mortality, anastomotic stenosis, recurrent laryngeal nerve injury, chylothorax, pulmonary complications, arrhythmia, delayed gastric emptying and total complications.

Quality assessment

Quality assessment was performed using the Newcastle-Ottawa quality assessment scale (NOS). The scale comprises 8 items divided into three parts: selection (maximum score, 4), comparability (maximum score, 2), and outcome (maximum score, 3) and which in total can give a maximum score of 9 points. The total score of 7 or more points was considered to indicate a high quality of the study, 6 points medium quality, and less than 6 points indicate low quality. Only studies with high and medium quality were finally enrolled. The assessment process was carried out independently by two assessors (J Wang and J Hu). Any disagreement was discussed with the third assessor until an agreement was reached.

Statistical analysis

Statistical analysis of the data was conducted using the Review Manager 5.3 software. The heterogeneity between the studies was analyzed by the I2 test, and I2>50% was considered to indicate significant heterogeneity between the studies. When significant heterogeneity was present between the studies, DerSimonian and Laird random effects model or Mantel-Haenszel fixed effect model was chosen. For binary variable results, the odds ratio (OR) and 95% confidence interval (CI) were calculated. For continuous variables, the mean difference and 95% CI were computed. P<0.05 was considered as statistically significant. Sensitivity analysis was performed on variables with significant heterogeneity using the Stata 15 statistical package to identify the source of heterogeneity. The publication bias of variables with the number of studies >10 was tested using the Egger’s test. The trim-and-fill method was used to further test the influence of publication bias on the results.


Results

Literature search and quality assessment

The retrieval and screening process of the references is shown in Figure 1. The retrieval strategy used identified 5,728 studies, of which 4,108 remained after removing duplicate publications. After reading the titles and abstracts, 4,028 studies that were evidently unrelated to the present analysis were eliminated. Full text of the remaining 80 studies was downloaded for further detailed reviews. Finally, the meta-analysis was conducted on the 23 studies that met the inclusion criteria. The characteristics and quality assessment scores of these 23 investigations are listed in Table S1. The quality assessment scores for all studies were above 6, meeting the inclusion criteria (8-30).

Figure 1 Summary of screening and selection process.

Results of meta-analysis

Primary outcome measures

Anastomotic leakage

A total of 23 publications reported the occurrence rate of anastomotic leakage. However, the report by Luketich et al. (21) provided only the incidence of anastomotic leakage requiring surgery, making it impossible to combine it with the other studies. This necessitated a separate meta-analysis of the occurrence rate of anastomotic leakage requiring surgery (see below). The 22 studies which listed the incidence of anastomotic leakage included 3,922 patients. The occurrence rate of anastomotic leakage was 14.7% in MIME, and 5.5% in MILE. The heterogeneity between the 22 studies was not statistically significant (P=0.09; I2=30%). Therefore, the fixed-effect model was adopted to compare the outcomes of the two protocols. This analysis indicated that the occurrence rate of anastomotic leakage was higher in MIME than that in MILE (OR =2.97, 95% CI: 2.34–3.77), and this difference was statistically significant (P<0.00001) (Figure 2).

Figure 2 Forest plot anastomotic leakage. CI, confidence interval; M-H, Mantel-Haenszel.

Three studies, reporting on 1,541 patients, included the data on the incidence of anastomotic leakage requiring surgery. The heterogeneity between the studies was not statistically significant (P=0.51; I2=0%); therefore, the fixed-effect model was chosen for analysis, which indicated that the occurrence rate of anastomotic leakage requiring surgery was significantly higher in MIME than in MILE (OR =1.57, 95% CI: 1.02–2.43, P=0.04) (Figure 3).

Figure 3 Forest plot anastomotic leakage requiring surgery. CI, confidence interval; M-H, Mantel-Haenszel.

Secondary outcome measures

Intraoperative data

The results of the meta-analysis of intraoperative data are shown in Table 1. The operating time was reported in 20 studies that included 3,478 patients. Meta-analysis documented that the operating time of MIME was longer than that of MILE [weighted mean difference (WMD) =23.69, 95% CI: 6.26–41.12, P=0.008]. There was no statistically significant difference between the two surgical procedures in terms of blood loss, the number of lymph nodes detected, transfusion rate, and R0 resection rate.

Table 1

Meta-analysis for intraoperative data

Outcomes No. of studies No. of patients McKeown’s events incidence (%) Ivor Lewis’s events incidence (%) WMD/OR (95% CI) Heterogeneity Test for overall effect Favors group
Operating time 20 3,478 23.69 (6.26, 41.12) I2=98%, P<0.00001 Z=2.66, P=0.008 Ivor Lewis
Blood loss 18 3,005 7.73 (−2.21, 17.59) I2=71%, P<0.00001 Z=1.54, P=0.12
Examined lymph nodes 17 4,231 0.69 (−0.62, 2.01) I2=87%, P<0.00001 Z=1.03, P=0.30
R0 resection 5 2,095 97.2% 96.8% 1.07 (0.63, 1.80) I2=0%, P=0.67 Z=0.24, P=0.81
Conversion to open 3 1,616 4.5% 3.6% 1.32 (0.80, 2.18) I2=0%, P=0.92 Z=1.08, P=0.28
Blood transfusion 5 984 3.5% 5.0% 0.79 (0.41, 1.50) I2=0%, P=0.54 Z=0.73, P=0.46

WMD, weighted mean difference; OR, odds ratio; CI, confidence interval.

Postoperative data

The results of the meta-analysis of postoperative data are listed in Table 2. In comparison with MILE, MIME was associated with a longer length of hospital stay (WMD =1.13, 95% CI: 0.45–1.82, P=0.001), higher in-hospital mortality (OR =2.83, 95% CI: 1.35–5.93, P=0.006), higher 30-day mortality (OR =2.44, 95% CI: 1.33–4.50, P=0.004), higher 90-day mortality (OR =2.85, 95% CI: 1.55–5.23, P=0.0007), but the cost of MIME was lower (WMD =−0.40, 95% CI: −0.74 to 0.07, P=0.02). The re-operation rate, drainage duration, length of stay in the ICU, and 1-year mortality were not statistically different between the two surgical procedures.

Table 2

Meta-analysis for postoperative data

Outcomes No. of studies No. of patients McKeown’s events incidence (%) Ivor Lewis’s events incidence (%) WMD/OR (95% CI) Heterogeneity Test for overall effect Favors group
Reoperations 4 836 14.0% 6.9% 1.57 (0.98, 2.53) I2=26%, P=0.25 Z=1.87, P=0.06
Drainage time 12 2,093 −0.41 (−1.33, 0.52) I2=94%, P<0.00001 Z=0.87, P=0.39
Hospital LOS 20 4,331 1.13 (0.45, 1.82) I2=82%, P<0.00001 Z=3.23, P=0.001 Ivor Lewis
ICU LOS 5 1,916 0.17 (−1.07, 1.41) I2=95%, P<0.00001 Z=0.27, P=0.79
Cost 9 1,817 −0.40 (−0.74, −0.07) I2=87%, P<0.00001 Z=2.37, P=0.02 McKeown
In-hospital mortality 10 2,316 2.4% 0.9% 2.83 (1.35, 5.93) I2=0%, P=0.80 Z=2.75, P=0.006 Ivor Lewis
30-day mortality 6 2,179 3.4% 1.2% 2.44 (1.33, 4.50) I2=2%, P=0.40 Z=2.86, P=0.004 Ivor Lewis
90-day mortality 4 919 8.9% 3.2% 2.85 (1.55, 5.23) I2=0%, P=0.97 Z=3.39, P=0.0007 Ivor Lewis
1-year mortality 3 294 9.8% 9.3% 1.04 (0.48, 2.27) I2=0%, P=0.56 Z=0.11, P=0.92

WMD, weighted mean difference; OR, odds ratio; CI, confidence interval; LOS, length of stay.

Complications

The results of the meta-analysis of complications are presented in Table 3. Patients undergoing MIME had a higher morbidity associated with anastomotic stricture (OR =2.89, 95% CI: 1.97–4.24, P<0.00001), recurrent laryngeal nerve (RLN) injury (OR =5.63, 95% CI: 3.99–7.94, P<0.00001), chylothorax (OR =1.55, 95% CI: 1.01–2.38, P=0.04), pulmonary complications (OR =1.89, 95% CI: 1.54–2.32, P<0.00001) and overall complications (OR =1.90, 95% CI: 1.34–2.71, P=0.0004). There were no statistical differences in morbidity related to lung infection, cardiac arrhythmia and delayed gastric emptying between MIME and MILE.

Table 3

Meta-analysis for complications data

Outcomes No. of studies No. of patients McKeown’s events incidence (%) Ivor Lewis’s events incidence (%) WMD/OR (95% CI) Heterogeneity Test for overall effect Favors group
Anastomotic stricture 11 2,102 10.0% 4.1% 2.89 (1.97, 4.24) I2=25%, P=0.21 Z=5.43, P<0.00001 Ivor Lewis
RLN trauma 20 4,365 9.7% 1.7% 5.63 (3.99, 7.94) I2=0%, P=0.85 Z=9.86, P<0.00001 Ivor Lewis
Chylothorax 12 2,352 4.9% 3.1% 1.55 (1.01, 2.38) I2=0%, P=0.70 Z=2.03, P=0.04 Ivor Lewis
Pulmonary complications 14 2,736 25.4% 15.1% 1.89 (1.54, 2.32) I2=36%, P=0.09 Z=6.11, P<0.00001 Ivor Lewis
Lung infection 8 971 11.9% 7.7% 1.44 (0.69, 3.00) I2=52%, P=0.04 Z=0.96, P=0.34
Cardiac arrhythmia 10 1,789 6.0% 4.3% 1.39 (0.89, 2.18) I2=0%, P=0.69 Z=1.44, P=0.15
Delayed gastric emptying 9 1,537 4.8% 3.9% 1.33 (0.80, 2.23) I2=36%, P=0.13 Z=1.09, P=0.28
Overall complications 13 2,861 43.8% 29.7% 1.90 (1.34, 2.71) I2=74%, P<0.00001 Z=3.57, P=0.0004 Ivor Lewis

WMD, weighted mean difference; OR, odds ratio; CI, confidence interval; RLN, recurrent laryngeal nerve.

Sensitivity analysis

Evident heterogeneity was present in the nine groups of studied variables, including operating time (I2=98%, P<0.00001), blood loss (I2=71%, P<0.00001), number of detected lymph nodes (I2=87%, P<0.00001), drainage duration (I2=94%, P<0.00001), length of hospital stay (I2=82%, P<0.00001), length of the stay in ICU (I2=95%, P<0.00001), cost (I2=87%, P<0.00001), lung infection (I2=52%, P=0.04), and total complications (I2=74%, P<0.00001). The sensitivity analysis for blood loss, drainage duration, length of hospital stay, length of the stay in ICU, cost and lung infection produced stable results, indicating that there was no source of heterogeneity. The sensitivity analysis of operating time showed that studies by Tang et al. (16) and van Workum et al. (18) significantly influenced the combined OR and CI. However, when these studies were removed, there was no evident change in heterogeneity (I2=98%, P<0.00001). The sensitivity analysis of the number of detected lymph nodes suggested that the study by Luketich et al. (21) significantly affected the final result. After eliminating this study, significant heterogeneity continued to be present (I2=75%, P<0.00001). Sensitivity analysis pointed to the publication of Tang et al. as the source of heterogeneity in meta-analysis of total complications. After removing this study, the heterogeneity of the results disappeared (I2=0%, P<0.66), and the results were: OR =1.55, 95% CI: 1.30–1.85, Z=4.83, P<0.00001.

Publication bias

The Egger’s test revealed that there was publication bias affecting the results of operating time, length of hospital stay, anastomotic stenosis, and anastomotic leakage. However, the trim-and-fill analysis indicated that the publication bias did not affect significantly the conclusions.


Discussion

This systematic review and meta-analysis compare the short-term effects of MIME and MILE. The present study reveals for the first time that MILE is superior to MIME in in-hospital mortality, 30-day mortality, 90-day mortality, the incidence of chylothorax, severe anastomotic leakage, and total complications, but is associated with a higher cost. The analysis confirmed previous findings that MILE provides better outcomes of operating time, length of hospital stay, anastomotic leakage, anastomotic stenosis, RLN injury, pulmonary complications.

In the comparison of intra-operative data, only identified difference between the two surgical procedures was the shorter operating time in MILE, since the neck incision is not necessary with this protocol. Among the postoperative complications, the lifted length of the tubular stomach was shorter in MILE, reducing the tension of anastomotic stoma and providing a better blood supply. Additionally, the anastomotic stoma inside the thorax was less compressed than the anastomotic stoma in the narrow cervical region, decreasing the likelihood of anastomotic leakage and anastomotic stenosis. Since the neck incision was not required for MILE, the exposure of the recurrent cervical laryngeal nerve was avoided, decreasing the morbidity associated with RLN injury. The morbidity of pulmonary complications after MILE was also lower, likely due to the shorter operating and RLN injury (31,32). MILE dissociated the proximal esophagus, which was lower than that in MIME, so it had less chance to damage the thoracic duct and reduced the morbidity of chylothorax (10). The meta-analysis of postoperative data indicated that MILE had lower morbidity associated with postoperative complications, resulting in a shorter length of hospital stay, and lower in-hospital mortality, 30-day mortality, and 90-day mortality. In MILE, anastomat was used for intrathoracic esophageal anastomosis, which may increase the cost (12). Importantly, all the relevant data were from Chinese research.

A remarkable aspect of the present analysis is the demonstration of the survival benefit of MILE. Mortality is an important indicator of the outcome of the surgery mode, highlighting the significance of the comparison of MILE and MIME. The absence of a statistically significant difference in 1-year mortality may reflect the small number of enrolled studies and cases was.

In comparison with previously published meta-analyses, more perfect improved strategies were developed, which not only enhanced the effectiveness of the search, but also retrieved the Chinese database. As a result, 23 medium and high-quality studies with 4,933 patients were enrolled in the meta-analysis. More outcome indexes were collected and analyzed, and the differences between the two procedures were analyzed in a more comprehensive way. The current meta-analysis detected also more differences between the two surgical approaches than previously published studies. Of note, a sensitivity analysis was performed for the results with significant heterogeneity, and the sources of heterogeneity were identified.

Some limitations of the present study should be acknowledged: (I) The analysis included only cohort studies so that the selection bias was unavoidable. (II) Long-term survival data were not available in the enrolled studies, making the assessment of the difference in long-term prognosis between MILE and MIME impossible. This limitation emphasized the need for new relevant clinical studies to determine the long-term survival after these two surgical protocols. (III) The homogeneity test of continuous variables demonstrated a significant heterogeneity. It may be caused by differences in experience and skills among the surgeons, and variations in the diagnosis and treatment protocols between different geographic regions. (IV) Among the 23 studies enrolled in the research, 18 were performed in China. Thus, the results of the present study may not serve as a reference for other countries and regions of the world.


Conclusions

MILE is superior to MIME in operating time, length of hospital stay, in-hospital mortality, 30-day mortality, 90-day mortality, anastomotic leakage, anastomotic leakage requiring surgery, anastomotic stenosis, RLN injury, chylothorax, pulmonary complications, total complications. However, MILE is associated with a higher cost. Therefore, MILE may represent a better option for MIE if economic conditions are not a limiting factor. It is worth noting that presented the meta-analysis is based on nonrandom cohort studies that have inherent selection bias and, therefore, should be interpreted cautiously. A large number of high-quality randomized controlled trials should be done to verify the results.

Supplementary

PubMed and Medline search strategy

#1, "Esophageal Neoplasms"[Mesh]

#2, Esophageal Neoplasm

#3, Neoplasm, Esophageal

#4, Esophagus Neoplasm

#5, Esophagus Neoplasms

#6, Neoplasm, Esophagus

#7, Neoplasms, Esophagus

#8, Neoplasms, Esophageal

#9, "Cancer of Esophagus"

#10, "Cancer of the Esophagus"

#11, Esophagus Cancer

#12, Cancer, Esophagus

#13, Cancers, Esophagus

#14, Esophagus Cancers

#15, Esophageal Cancer

#16, Cancer, Esophageal

#17, Cancers, Esophageal

#18, Esophageal Cancers

#19, "Esophagectomy"[Mesh]

#20, Esophagectomies

#21, Oesophagectomy

#22, Oesophagectomies

#23, #1 OR #2 OR #3 OR #4 OR #5 OR #6 OR #7 OR #8 OR #9 OR #10 OR #11 OR #12 OR #13 OR #14 OR #15 OR #16 OR #17 OR #18 OR #19 OR #20 OR #21 OR #22

#24, "Video-Assisted Surgery"[Mesh]

#25, Surgeries, Video-Assisted

#26, Video Assisted Surgery

#27, Video-Assisted Surgeries

#28, Surgery, Video-Assisted

#29, Surgery, Video Assisted

#30, "Thoracic Surgery, Video-Assisted"[Mesh]

#31, Surgeries, Video-Assisted Thoracic

#32, Surgery, Video-Assisted Thoracic

#33, Thoracic Surgeries, Video-Assisted

#34, Thoracic Surgery, Video Assisted

#35, Video-Assisted Thoracic Surgeries

#36, Video-Assisted Thoracoscopic Surgery

#37, Surgeries, Video-Assisted Thoracoscopic

#38, Surgery, Video-Assisted Thoracoscopic

#39, Thoracoscopic Surgeries, Video-Assisted

#40, Thoracoscopic Surgery, Video-Assisted

#41, Video Assisted Thoracoscopic Surgery

#42, Video-Assisted Thoracoscopic Surgeries

#43, Video-Assisted Thoracic Surgery

#44, Video Assisted Thoracic Surgery

#45, Surgery, Thoracic, Video-Assisted

#46, VATS

#47, VATSs

#48, "Minimally Invasive Surgical Procedures"[Mesh]

#49, Surgical Procedures, Minimal

#50, Surgical Procedures, Minimal Access

#51, Surgical Procedures, Minimally Invasive

#52, Minimal Access Surgical Procedures

#53, Minimal Surgical Procedure

#54, Procedures, Minimally Invasive Surgical

#55, Minimally Invasive Surgery

#56, Surgeries, Minimally Invasive

#57, Surgery, Minimally Invasive

#58, Procedure, Minimal Surgical

#59, Procedures, Minimal Access Surgical

#60, Procedures, Minimal Surgical

#61, Surgical Procedure, Minimal

#62, Minimal Surgical Procedures

#63, #24 OR #25 OR #26 OR #27 OR #28 OR #29 OR #30 OR #31 OR #32 OR #33 OR #34 OR #35 OR #36 OR #37 OR #38 OR #39 OR #40 OR #41 OR #42 OR #43 OR #44 OR #45 OR #46 OR #47 OR #48 OR #49 OR #50 OR #51 OR #52 OR #53 OR #54 OR #55 OR #56 OR #57 OR #58 OR #59 OR #60 OR #61 OR #62

#64, #23 AND #63

#65, #64 OR McKeown OR Ivor Lewis

#66, "Cohort Studies"[Mesh]

#67, Cohort Study

#68, Studies, Cohort

#69, Study, Cohort

#70, Concurrent Studies

#71, Studies, Concurrent

#72, Concurrent Study

#73, Study, Concurrent

#74, Closed Cohort Studies

#75, Cohort Studies, Closed

#76, Closed Cohort Study

#77, Cohort Study, Closed

#78, Study, Closed Cohort

#79, Studies, Closed Cohort

#80, Analysis, Cohort

#81, Cohort Analysis

#82, Analyses, Cohort

#83, Cohort Analyses

#84, Historical Cohort Studies

#85, Cohort Study, Historical

#86, Historical Cohort Study

#87, Study, Historical Cohort

#88, Incidence Studies

#89, Incidence Study

#90, Studies, Incidence

#91, Study, Incidence

#92, #66 OR #67 OR #68 OR #69 OR #70 OR #71 OR #72 OR #73 OR #74 OR #75 OR #76 OR #77 OR #78 OR #79 OR #80 OR #81 OR #82 OR #83 OR #84 OR #85 OR #86 OR #87 OR #88 OR #89 OR #90 OR #91

#93, #65 AND #92

Embase search strategy

#1, 'esophagus tumor'/exp

#2, 'esophageal neoplasms'

#3, 'esophageal tumor'

#4, 'esophagus tumor'

#5, 'esophagus tumour'

#6, 'oesophageal neoplasms'

#7, 'oesophageal tumor'

#8, 'oesophageal tumour'

#9, 'oesophagus tumor'

#10, 'oesophagus tumour'

#11, 'tumor, esophagus'

#12, 'tumour, esophagus'

#13, #1 OR #2 OR #3 OR #4 OR #5 OR #6 OR #7 OR #8 OR #9 OR #10 OR #11 OR #12

#14, 'endoscopic surgery'/exp

#15, 'endoscopic resection'

#16, 'endoscopic surgery'

#17, 'resection, endoscopic'

#18, 'surgery, endoscopic'

#19, 'surgery, video assisted'

#20, 'surgical procedures, endoscopic'

#21, 'video-assisted surgery'

#22, 'video assisted thoracoscopic surgery'/exp

#23, 'vats'

#24, 'thoracic surgery, video-assisted'

#25, 'video assisted thoracic surgery'

#26, 'video assisted thoracoscopic surgery'

#27, 'videothoracoscopic surgery'

#28, 'minimally invasive surgery'/exp

#29, 'mini-invasive surgery'

#30, 'mini-invasive surgical procedure'

#31, 'mini-invasive surgical procedures'

#32, 'minimally invasive surgery'

#33, 'minimally invasive surgical method'

#34, 'minimally invasive surgical methods'

#35, 'minimally invasive surgical procedure'

#36, 'minimally invasive surgical procedures'

#37, 'minimally invasive surgical technique'

#38, 'minimally invasive surgical techniques'

#39, 'surgery, minimally invasive'

#40, 'surgical procedures, minimally invasive'

#41, #14 OR #15 OR #16 OR #17 OR #18 OR #19 OR #20 OR #21 OR #22 OR #23 OR #24 OR #25 OR #26 OR #27 OR #28 OR #29 OR #30 OR #31 OR #32 OR #33 OR #34 OR #35 OR #36 OR #37 OR #38 OR #39 OR #40

#42, #13 AND #41

#43, #42 OR 'McKeown' OR 'ivor lewis'

#44, 'cohort analysis'/exp

#45, 'analysis, cohort'

#46, 'cohort analysis'

#47, 'cohort fertility'

#48, 'cohort life cycle'

#49, 'cohort studies'

#50, 'cohort study'

#51, 'fertility, cohort'

#52, #44 OR #45 OR #46 OR #47 OR #48 OR #49 OR #50 OR #51

#53, #43 AND #52

The Cochrane Library search strategy

#1, MeSH descriptor: [Esophageal Neoplasms] explode all trees

#2, MeSH descriptor: [Esophagectomy] explode all trees

#3, Oesophagectomy

#4, Oesophagectomies

#5, #1 OR #2 OR #3 OR #4

#6, MeSH descriptor: [Video-Assisted Surgery] explode all trees

#7, MeSH descriptor: [Thoracic Surgery, Video-Assisted] explode all trees

#8, MeSH descriptor: [Minimally Invasive Surgical Procedures] explode all trees

#9, #6 OR #7 OR #8

#10, #5 AND #9

#11, #10 OR McKeown OR Ivor Lewis

Wanfang Databases, China National Knowledge Infrastructure (CNKI) and Chinese VIP Information search strategy

#1, McKeown

#2, Ivor Lewis

#3, Ivor-Lewis

#4, #1 OR #2 OR #3

Table S1

The characteristics and quality assessment scores of included studies

Study Study interval Study type Country Total cases Group Number Sex (M/F) Age (mean ± SD) Location of cancer Outcome parameters Quality score
Brown et al., 2018 June 2011 to May 2016 Prospective cohort USA 110 McKeown 61 51/10 63±8.7 All segments Duration of surgery, blood loss, examined LN, examined LN positive, R0 resection, hospital length of stay, cost, in-hospital mortality, 30-day mortality, anastomotic leakage, RLN injury, chylothorax, cardiac complications, pulmonary complications, delayed gastric emptying, thromboembolism, urinary tract complications, wound infection, 90 days, 180 days of serious complications 7
Ivor Lewis 49 40/9 60.9±9.0
Chang, 2018 January to December 2015 Retrospective cohort China 53 McKeown 33 NA NA All segments Reoperations, ICU length of stay, hospital length of stay, 30-day mortality, 90-day mortality, anastomotic leakage, anastomotic stenosis, RLN injury, cardiac arrhythmia, pulmonary complications 6
Ivor Lewis 20 NA NA
Chen et al., 2017 2014–2016 Prospective cohort China 251 McKeown 51 38/13 61.4±9.1 All segments Duration of surgery, blood loss, examined LN, conversion to open, R0 resection, hospital length of stay, reoperations, 30-day mortality, ICU stay, anastomotic leakage, anastomotic stenosis, chylothorax, cardiac arrhythmia, RLN injury 7
Ivor Lewis 200 169/31 59.9±8.4
Gao, 2016 February 2012 to January 2015 Retrospective cohort China 158 McKeown 77 41/36 57.3±5.9 All segments Duration of surgery, blood loss, examined LN, drainage time, 6-month tumor recurrence, anastomotic leakage, RLN injury, cardiac arrhythmia, pulmonary infection 8
Ivor Lewis 81 44/37 59.6±6.8
Hao et al., 2014 June 2008 to June 2012 Retrospective cohort China 136 McKeown 81 NA NA All segments Duration of surgery, blood loss, examined LN, hospital length of stay, in-hospital mortality, anastomotic leakage 6
Ivor Lewis 55 NA NA
Hou et al., 2017 2014 l January to May 2016 Retrospective cohort China 185 McKeown 65 41/24 56.7±11.6 All segments Duration of surgery, blood loss, examined LN, serious intraoperative complications, conversion to open, R0 resection, hospital length of stay, cost, in-hospital mortality, anastomotic leakage, RLN injury, respiratory complications, cardiovascular complications, postoperative bleeding, other complications, postoperative pain, quality of life score 8
Ivor Lewis 120 82/38 57.2±13.0
Huang, 2017 January 2015 to December 2016 Prospective cohort China 200 McKeown 100 59/41 56.2±6.3 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, cost, in-hospital mortality, tumor recurrence, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, cardiac arrhythmia, pulmonary complications, delayed gastric emptying, esophageal reflux, incision infection 7
Ivor Lewis 100 61/39 57.5±7.1
Lin et al., 2014 December 2010 to March 2014 Retrospective cohort China 288 McKeown 185 142/43 58.3±8.7 Middle and low segments Duration of surgery, blood loss, examined LN, blood transfusion, drainage time, postoperative feeding time, ICU stay, hospital length of stay, cost, in-hospital mortality, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, cardiac arrhythmia, pulmonary complications, delayed gastric emptying, incision bleeding 8
McKeown 103 80/23 59.1±8.4
Ling, 2018 January 2014 to April 2017 Retrospective cohort China 129 McKeown 56 43/13 61.5±18.1 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, cost, 6-months tumor recurrence, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, pulmonary infection, atelectasis, delayed gastric emptying 8
Ivor Lewis 73 55/18 63.2±17.8
Luketich et al., 2012 August 1996 to March 2011 Retrospective cohort USA 1,011 McKeown 481 392/89 65 [56–72] All segments Examined LN, conversion to open, R0 resection, ICU length of stay, hospital length of stay, ICU length of stay, 30-day mortality, anastomotic leakage, RLN injury, cardiac complications, ARDS, empyema, gastric tube necrosis 7
Ivor Lewis 530 415/115 64 [56–72]
Mei, 2016 January 2012 to September 2015 Retrospective cohort China 106 McKeown 65 49/16 63.56±5.09 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, cost, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, pulmonary infection, incision infection 8
Ivor Lewis 41 32/9 62.71±5.04
Meng, 2016 March 2011 to June 2014 Retrospective cohort China 47 McKeown 26 16/10 56.8±7.2 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, in-hospital mortality, anastomotic leakage, anastomotic stenosis, RLN injury, pulmonary infection, esophageal reflux 8
Ivor Lewis 21 13/8 57.3±6.4
Nguyen et al., 2008 August 1998 to September 2007 Prospective cohort USA 98 McKeown 47 39/8 65±10 All segments Duration of surgery, blood loss, blood transfusion, ICU length of stay, hospital length of stay, 30-Day mortality, anastomotic leakage, anastomotic stenosis, major complications 6
Ivor Lewis 51 33/18 64±12
Ren, 2018 March 2013 to July 2016 Prospective cohort China 82 McKeown 41 31/10 59.0±7.5 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, cost, 1-year mortality, 1-year tumor recurrence, anastomotic leakage, RLN injury, cardiac arrhythmia, pulmonary complications, delayed gastric emptying, incision bleeding 9
Ivor Lewis 41 31/10 57.2±8.0
Rong et al., 2018 March to November 2017 Retrospective cohort China 130 McKeown 65 46/19 NA Middle segments Duration of surgery, blood loss, examined LN, R0 resection, ICU stay, hospital length of stay, cost, in-hospital mortality, anastomotic leakage, RLN injury, chylothorax, pulmonary infection 6
Ivor Lewis 65 52/13 NA
Schmidt et al., 2017 June 2011 to May 2016 Retrospective cohort Switzerland 334 McKeown 146 NA NA All segments Examined LN, R0 resection, hospital length of stay, 30-day mortality, 90-day mortality, ICU length of stay, hospital readmission, anastomotic leakage, cardiac complications, pulmonary complications 7
Ivor Lewis 188 NA NA
Sun, 2017 May 2014 to May 2015 Retrospective cohort China 92 McKeown 42 NA NA Middle and low segments Duration of surgery, blood loss, examined LN, examined LN positive, drainage time, hospital length of stay, cost, 1-year mortality, 1-year tumor metastasis, anastomotic leakage, RLN injury, pulmonary complications, cardiac arrhythmia, delayed gastric emptying, incision bleeding 8
Ivor Lewis 50 NA NA
Tang et al., 2016 December 2013 to April 2015 Retrospective cohort China 433 McKeown 278 201/77 57.1±6.9 Middle and low segments Duration of surgery, blood loss, examined LN, blood transfusion, drainage time, postoperative feeding time, hospital length of stay, cost, in-hospital mortality, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, cardiac arrhythmia, pulmonary complications, delayed gastric emptying 8
Ivor Lewis 155 103/52 55.8±7.1
Wei et al., 2016 January 2013 to June 2015 Prospective cohort China 120 McKeown 50 31/19 59.69±8.31 Middle and low segments Duration of surgery, blood loss, examined LN, conversion to open, drainage time, hospital length of stay, in-hospital mortality, 1-year mortality, anastomotic leakage, RLN injury, chylothorax, cardiac arrhythmia, pulmonary complications, delayed gastric emptying, incision bleeding, pain score 24 hours after surgery, pain score 72 hours after surgery, time to get out of bed, anal exhaust time 9
Ivor Lewis 70 47/23 55.69±6.15
Workum et al., 2018 November 2009 to April 2017 Retrospective cohort The Netherlands 420 McKeown 210 169/41 NA Low segment and gastroesophageal junction Duration of surgery, examined LN, conversion to open, R0 resection, reintervention, ICU length of stay, hospital length of stay, in-hospital mortality, 30-day mortality, 90-day mortality, anastomotic leakage, RLN injury, chylothorax, cardiac complications, pulmonary complications, jejunostomy-related complications, overall complications, 30-day hospital readmission 8
Ivor Lewis 210 176/34 NA
Wu et al., 2014 October 2011 to March 2014 Retrospective cohort China 357 McKeown 138 106/32 63.52±17.6 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, hospital length of stay, cost, In-hospital mortality, tumor recurrence, anastomotic leakage, anastomotic stenosis, RLN injury 8
Ivor Lewis 219 169/50 61.8±18.5
Zhai, 2016 January 2013 to June 2015 Retrospective cohort China 112 McKeown 62 56/6 60.8±1.3 Middle and low segments Duration of surgery, blood loss, examined LN, blood transfusion, ICU stay, hospital length of stay, reoperations, 90-day mortality, anastomotic leakage, anastomotic stenosis, RLN injury, chylothorax, pulmonary complications, delayed gastric emptying 8
Ivor Lewis 50 46/4 59.3±1.2
Zhang et al., 2018 October 2015 to September 2017 Retrospective cohort China 81 McKeown 49 26/23 49.41±9.63 Middle and low segments Duration of surgery, blood loss, examined LN, drainage time, drainage volume, hospital length of stay, anastomotic leakage, anastomotic stenosis, RLN injury, pulmonary infection, delayed gastric emptying 7
Ivor Lewis 32 17/15 51.76±6.98

NA, not available; M/F, male/female; SD, standard deviation; LN, lymph nodes; RLN, recurrent laryngeal nerve; ICU, intensive care unit.


Acknowledgments

We would like to thank Guangqi Qin, PhD and Jiao Liu, PhD, for their help with correcting the manuscript and providing valuable support and comments during our scientific research.

Funding: None.


Footnote

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2020.01.45). 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.

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/.


References

  1. Torre LA, Siegel RL, Ward EM, et al. Global Cancer Incidence and Mortality Rates and Trends--An Update. Cancer Epidemiol Biomarkers Prev 2016;25:16-27. [Crossref] [PubMed]
  2. Takahashi C, Shridhar R, Huston J, et al. Esophagectomy from then to now. J Gastrointest Oncol 2018;9:903-9. [Crossref] [PubMed]
  3. Lagergren J, Smyth E, Cunningham D, et al. Oesophageal cancer. Lancet 2017;390:2383-96. [Crossref] [PubMed]
  4. Rustgi AK, El-Serag HB. Esophageal carcinoma. N Engl J Med 2014;371:2499-509. [Crossref] [PubMed]
  5. Gisbertz SS, Hagens ERC, Ruurda JP, et al. The evolution of surgical approach for esophageal cancer. Ann N Y Acad Sci 2018;1434:149-55. [Crossref] [PubMed]
  6. Deng J, Su Q, Ren Z, et al. Comparison of short-term outcomes between minimally invasive McKeown and Ivor Lewis esophagectomy for esophageal or junctional cancer: a systematic review and meta-analysis. Onco Targets Ther 2018;11:6057-69. [Crossref] [PubMed]
  7. van Workum F, Berkelmans GH, Klarenbeek BR, et al. McKeown or Ivor Lewis totally minimally invasive esophagectomy for cancer of the esophagus and gastroesophageal junction: systematic review and meta-analysis. J Thorac Dis 2017;9:S826-33. [Crossref] [PubMed]
  8. Chen L, Liu X, Wang R, et al. Minimally invasive esophagectomy for esophageal cancer according to the location of the tumor: Experience of 251 patients. Ann Med Surg (Lond) 2017;17:54-60. [Crossref] [PubMed]
  9. Huang S. Minimally invasive Ivor-Lewis Vs McKeown esophagectomy in the treatment of lower thoracic esophageal cancer. J MED Theor Prac 2017;30:3189-91.
  10. Lin J, Kang M, Lin J, et al. Short-term efficacy comparison between Ivor-Lewis approach and McKeown approach in minimally invasive esophagectomy. Zhonghua Wei Chang Wai Ke Za Zhi 2014;17:888-91. [PubMed]
  11. Meng Q. Clinical Analysis of Minimal Invasive McKeown and Ivor-Lewis Surgery in the Treatment of Middle-Lower Section Esophageal Cancer. Medical Innovation of China 2016;13:17-20.
  12. Wu H, Xie M, Liu C, et al. A retrospective study of short-term outcomes of minimally invasive Ivor-Lewis esophagectomy and McKeown esophagectomy for thoracic middle-lower esophageal carcinoma. Chin J Thorac Cardiovasc Surg 2014;30:649-52.
  13. Hou X, Ren Z, Yang B, et al. Comparison of short-term therapeutic efficacy between minimally invasive Ivor-Lewis esophagectomy and Mckeown esophagectomy for esophageal cancer. Biomed Res 2017;28:5321-6.
  14. Rong B. Comparison of Ivor-Lewis approach and Mckeown approach in treating mid-thoracic esophageal cancer. Chin J Clin Healthc 2018;21:497-500.
  15. Wei H. The comparison of the clinical curative effect of Ivor-Lewis and McKeown operation in totally endoscopic esophagectomy. Chin J Thorac Cardiovasc Surg 2016;32:495-8.
  16. Tang X. Short-term effects of full-endoscopic Ivor-lews and Mckeown operations on treatment of thoracic middle-lower segment esophageal carcinoma. Medical Journal of National Defending Forces in Southwest China 2016;26:1173-5.
  17. Brown AM, Pucci MJ, Berger AC, et al. A standardized comparison of peri-operative complications after minimally invasive esophagectomy: Ivor Lewis versus McKeown. Surg Endosc 2018;32:204-11. [Crossref] [PubMed]
  18. van Workum F, Slaman AE, van Berge Henegouwen MI, et al. Propensity Score-Matched Analysis Comparing Minimally Invasive Ivor Lewis Versus Minimally Invasive Mckeown Esophagectomy. Ann Surg 2020;271:128-33. [Crossref] [PubMed]
  19. Sun Y. Feasibility, safety and short-term efficacy of thoracoscopy and laparoscopy combined with Ivor-Lewis surgery for middle and lower esophageal carcinoma. Hainan Med J 2017;28:576-7.
  20. Nguyen NT, Hinojosa MW, Smith BR, et al. Minimally invasive esophagectomy: lessons learned from 104 operations. Ann Surg 2008;248:1081-91. [Crossref] [PubMed]
  21. Luketich JD, Pennathur A, Awais O, et al. Outcomes after minimally invasive esophagectomy: review of over 1000 patients. Ann Surg 2012;256:95-103. [Crossref] [PubMed]
  22. Schmidt HM, Gisbertz SS, Moons J, et al. Defining Benchmarks for Transthoracic Esophagectomy: A Multicenter Analysis of Total Minimally Invasive Esophagectomy in Low Risk Patients. Ann Surg 2017;266:814-21. [Crossref] [PubMed]
  23. Hao Z, Zhenya S, Lei W. Esophageal-gastric anastomosis in radical resection of esophageal cancer under thoracoscopy combined with laparoscopy. J Coll Physicians Surg Pak 2014;24:754-6. [PubMed]
  24. Gao S, An ZY. Control study of the short-term efficacy of Ivor-Lewis and McKeown operation by thoracoscopy and laparoscopy in esophageal squamous cell carcinoma. Chinese Journal of the Frontiers of Medical Science 2016;8:57-60. (Electronic Version).
  25. Ling F. Short-term effects of full-endoscopic Ivor-lews Vs Mckeown esophagectomy on treatment of thoracic middle-lower segment esophageal carcinoma. Shandong Med J 2018;58:45-47.
  26. Zhang L, Chen M, Zhang Y. The effect of minimally invasive esophagectomy Mckeown and Ivor-Lewis on pulmonary function in patients with esophageal carcinoma. Oncology Progress 2018;16:1604-7.
  27. Ren W. Influence of Lvor-Lewis and McKeown surgery For middle and lower esophageal carcinoma in immune pain response, digestive function and prognosis. Pract J Clin Med 2018;15:246-8.
  28. Chang T, Hsiao PN, Tsai MY, et al. Perioperative management and outcomes of minimally invasive esophagectomy: case study of a high-volume tertiary center in Taiwan. J Thorac Dis 2018;10:1670-6. [Crossref] [PubMed]
  29. Zhai C. A comparison of short-term outcomes and quality of life between Ivor-Lewis and McKeown minimally invasive esophagectomy. Shandong University, 2016.
  30. Mei S. Short-term efficacy of purse sting forceps Ivor-Lewis approach and McKeown approach in minially invasive esophagectomy for middle-lower section esophageal cancer. Anhui Medical University, 2016.
  31. Inokuchi M, Kojima K, Kato K, et al. Risk factors for post-operative pulmonary complications after gastrectomy for gastric cancer. Surg Infect (Larchmt) 2014;15:314-21. [Crossref] [PubMed]
  32. Scholtemeijer MG, Seesing MFJ, Brenkman HJF, et al. Recurrent laryngeal nerve injury after esophagectomy for esophageal cancer: incidence, management, and impact on short- and long-term outcomes. J Thorac Dis 2017;9:S868-78. [Crossref] [PubMed]
Cite this article as: Wang J, Hu J, Zhu D, Wang K, Gao C, Shan T, Yang Y. McKeown or Ivor Lewis minimally invasive esophagectomy: a systematic review and meta-analysis. Transl Cancer Res 2020;9(3):1518-1527. doi: 10.21037/tcr.2020.01.45

Download Citation