Literature DB >> 28836986

Robotic versus laparoscopic Gastrectomy for gastric cancer: a systematic review and updated meta-analysis.

Ke Chen1, Yu Pan1, Bin Zhang1, Hendi Maher2, Xian-Fa Wang1, Xiu-Jun Cai3.   

Abstract

BACKGROUND: Advanced minimally invasive techniques including robotic surgery are being employed with increasing frequency around the world, primarily in order to improve the surgical outcomes of laparoscopic gastrectomy (LG). We conducted a systematic review and meta-analysis to evaluate the feasibility, safety and efficacy of robotic gastrectomy (RG).
METHODS: Studies, which compared surgical outcomes between LG and RG, were retrieved from medical databases before May 2017. Outcomes of interest were estimated as weighted mean difference (WMD) or risk ratio (RR) using the random-effects model. The software Review Manage version 5.1 was used for all calculations.
RESULTS: Nineteen comparative studies with 5953 patients were included in this analysis. Compared with LG, RG was associated with longer operation time (WMD = -49.05 min; 95% CI: -58.18 ~ -39.91, P < 0.01), less intraoperative blood loss (WMD = 24.38 ml; 95% CI: 12.32 ~ 36.43, P < 0.01), earlier time to oral intake (WMD = 0.23 days; 95% CI: 0.13 ~ 0.34, P < 0.01), and a higher expense (WMD = -3944.8 USD; 95% CI: -4943.5 ~ -2946.2, P < 0.01). There was no significant difference between RG and LG regarding time to flatus, hospitalization, morbidity, mortality, harvested lymph nodes, and cancer recurrence.
CONCLUSIONS: RG can be performed as safely as LG. However, it will take more effort to decrease operation time and expense.

Entities:  

Keywords:  Gastrectomy; Laparoscopy; Meta-analysis; Morbidity; Robot; Stomach neoplasms

Mesh:

Year:  2017        PMID: 28836986      PMCID: PMC5571509          DOI: 10.1186/s12893-017-0290-2

Source DB:  PubMed          Journal:  BMC Surg        ISSN: 1471-2482            Impact factor:   2.102


Background

Laparoscopic gastrectomy (LG) has been widely used for the treatment of gastric cancer and a number of other different minimally invasive procedures have been developed to date [1, 2]. There are several benefits for patients; including better cosmesis, reduced pain, early recovery of intestinal function, and shorter hospital stay, while maintaining comparable oncologic safety [1-4]. Robotic surgery was first put into practice in 2000, after being approved by the US Food and Drug Administration (FDA). It plays an essential role in ergonomics and offers advantages such as motion scaling, less fatigue, tremor filtering, seven degrees of wrist-like motion, and three-dimensional vision [5, 6]. Surgeons hoped that such innovative technology could overcome some limitations innate to traditional laparoscopic surgery. Thus, experienced laparoscopic surgeons are increasingly trying to develop new procedures that best exploit the capabilities of robotic surgery in the treatment of gastric cancer [7]. Nonetheless, the present status of robotic gastrectomy (RG) is, as of the writing of this paper, still restricted and this is in part to due to the lack of randomized controlled trials (RCTs). Several previous studies including meta-analyses have argued that RG can be a more effective and safer operation in comparison with conventional LG. In spite of these studies, many questions still need to be answered, most notably, RG’s efficacy with regard to oncologic, long-term survival outcomes and its cost-effectiveness. Moreover, a series of studies on RG for the treatments of gastric cancer have been recently published. These studies are meaningful in highlighting the status of RG in the treatment of gastric cancer. Therefore, this paper’s current research is intended to conduct a comprehensive systematic review of all the currently available literature and a meta-analysis of RG in comparison to LG in order to assess the feasibility, security and efficacy of RG.

Methods

Search strategy

A systematic search of Web of Science, Cochrane Library, Embase, and PubMed was conducted to find studies comparing RG and LG for gastric cancer treatment published up until May 2017. Search terms included “gastric carcinoma”, “gastric cancer”, “laparoscopic”, “robotic”, and “gastrectomy”. The links in search results and references were also reviewed to find the additional literature. Based on the language competencies of the reviewers, English and Chinese were the only languages of searched papers.

Eligibility criteria

The standards for research were comparative, using peer-reviewed studies of RG versus LG in gastric cancer for which the full texts were available. The most recent study or the study with the most subjects was chosen if overlapping research studies were found. Articles including any of the following were excluded: (1) Non-comparative studies such as letters, reviews, comments, posters, protocols, et al. (2) Studies including non-gastric carcinoma cases such as gastrointestinal stromal tumors, or benign gastric diseases; (3) Studies in which less than 2 of the interesting indices were reported.

Data extraction and quality assessment

Two reviewers (Chen K and Pan Y) reviewed the publications thoroughly and independently. Data extracted included the following items: author, region, operation time, intraoperative estimated blood loss (EBL), time to flatus, time to oral intake, length of hospital stay (LOS), morbidity, mortality, costs, retrieved lymph nodes (RLN), proximal and distal margin distance, and long-term oncologic outcomes. In accordance with the morbidity reporting system of Memorial Sloan-Kettering Cancer Center [8], postoperative complications were categorized into medical complications (respiratory, cardiovascular, metabolic events, deep venous thrombosis, phlebitis, et al.) or surgical complications (bleeding, any complication required reoperation, anastomotic leakage or stricture, delayed gastric emptying, et al.). The means and standard deviations (SDs) were estimated as described by Hozo et al. [9] if the research offered medians and ranges. The choice of the articles included in this review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement (PRISMA). The Newcastle-Ottawa Quality Assessment Scale (NOS) was utilized to evaluate the research quality (http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp). The scale ranges from 0 to 9 stars: research with a score higher than or equal to 6 could be deemed as methodologically sound.

Subgroup analysis

The uneven distribution of the surgical extension between the groups could affect the outcomes. Therefore, to eliminate the bias, a subgroup analysis of total or distal gastrectomy was conducted. It has been reported that robotic surgery may benefit obese patients, because of improved visualization, instrumentation, and ergonomics [10]. Therefore, we conducted a subgroup analysis to analyze the impact of operation-related factors on body mass index (BMI).

Statistical analysis

The risk ratio (RR) was utilized to analyze the dichotomous variables and the weighted mean difference (WMD) was utilized to assess the continuous variables. Based on DerSimonian and Laird’s approach, the random-effects model was utilized to account for clinical heterogeneity, which refers to diversity in a sense that is relevant for clinical situations. According to the overall complication, the potential publication bias was determined by carrying out an informal visual inspection of funnel plots. The software of Review Manager version 5.1 (RevMan 5.1) was used to conduct data analysis. P < 0.05 was considered statistically significant.

Results

Studies selected

A total of 378 potential articles, which were published from 1996 to 2017, were found. 37 articles were chosen based on the titles and abstracts, and then a thorough check of each text was conducted. Seven of them failed to meet our standards and were excluded. A further eleven papers were excluded due to overlapping patient cohorts (one from Hospital Niguarda Ca Granda, Italy [11]; one from Fujita Health University, Japan [12]; one from Taipei Veterans General Hospital, Taiwan [13]; four from Yonsei University, Korea [14-17]; four from National Cancer Center, Korea [18-21]). Finally, a total of nineteen studies were included for final meta-analysis [22-40]. A flow chart of the search strategies, which contains reasons for the exclusion of studies, is elucidated in Fig. 1.
Fig. 1

Flow chart of literature search strategies

Flow chart of literature search strategies

Study characteristics and quality

A total of 5953 patients were included in the analysis with 4123 undergoing LG (69.3%) and 1830 undergoing RG (30.7%). Most of the studies came from East Asia (10 Korea, 2 Japan, 4 China, 1 Taiwan) and 2 research studies came from Italy. The baseline features of the included studies are shown in Table 1; the evaluation of quality according to the NOS is shown in Table 2. NOS shows that four out of the 19 studies observed had 9 stars, one had 8 stars, seven had 7 stars and the remaining seven had 6 stars.
Table 1

Summary of studies included in the meta-analysis

AuthorRegionStudy designYearStudyperiodSample sizeLevel of lymphadenectomySurgical extensionReconstructionConversion (%)
LGRGLGRG
PuglieseItalyOCS (R)20102000–20094816D2DR-Y3(6)2(12)
Kim MCKoreaOCS (P)20102007–20081116D1 + β, D2DB-I, B-II00
Kim KMKoreaOCS (P)20122005–2010861436D1 + α/β, D2D, TB-I, B-II, R-YNRNR
Son SYKoreaOCS (R)20122007–20114221D1 + β, D2D, P, TB-I, B-II, R-YNRNR
KangKoreaOCS (P)20122008–2011282100D1 + α/β, D2D, TB-I, B-II, R-YE0
ZhangChinaOCS (R)20122009–20117097D2D, P, TB-I, B-II, R-Y00
HyunKoreaOCS (P)20132009–20108338D1 + α/β, D2D, TB-I, B-II, R-Y00
Son TKoreaOCS (R)20142003–20105851D2TR-Y00
NoshiroJapanOCS (P)20142010–201216021D1 + α/β, D2DB-I, B-II, R-Y00
HuangTaiwanOCS (P)20142008–20147372D1 + α/β, D2D, TB-I, R-YNRNR
ZhouChinaOCS (R)20142010–2013394120D1 + α/β, D2D, P, TB-I, B-II, R-YEE
LiuChinaOCS (R)20142012–2013100100D2D, P, TB-I, B-II, R-Y1(1)0
LeeKoreaOCS (P)20152003–2010267133D2DB-I, B-II, R-YNRNR
HanKoreaOCS (R)20152008–20136868D1 + βPPGGG00
ParkKoreaOCS (P)20152009–2011612145D1 + α/βD, TB-I, B-II, R-Y10(1.6)3(2.0)
SudaJapanOCS (R)20152009–201243888D1 + α/β, D2D, TB-I, B-II, R-Y00
Kim HIKoreaOCS (P)20162011–2012185185D1 + α/β, D2D, TB-I, B-II, R-Y2(1.1)1(0.5)
ShenChinaOCS (R)20162011–201433093D1 + α/β, D2D, TB-I, B-II, R-Y00
CianchiItalyOCS (R)20162008–20154130D1 + α/β, D2DB-II, R-Y00

OCS observational clinical study, P prospectively collected data, R retrospectively collected data, D distal gastrectomy, P proximal gastrectomy, T total gastrectomy, PPG pylorus-preserving gastrectomy, B-I Billroth-I, B-II Billroth-II, R-Y Roux-en-Y, GG gastro-gastro anastomosis, E exclude, NR not reported

Table 2

Quality assessment based on the NOS for observational studies

AuthorSelection (Out of 4)Comparability (Out of 2)Outcomes (Out of 3)Total (Out of 9)
Pugliese*********9
Kim MC******6
Kim KM******6
Son SY*******7
Kang******6
Zhang*******7
Hyun******6
Son T*********9
Noshiro*******7
Huang*******7
Zhou*********9
Liu*******7
Lee********8
Han*********9
Park******6
Suda*******7
Kim HI******6
Shen*******7
Cianchi******6

①representativeness of exposed cohort

②selection of nonexposed cohort

③ascertainment of exposure

④outcome not present at the start of the study

⑤assessment of outcomes

⑥length of follow-up

⑦adequacy of follow-up

Summary of studies included in the meta-analysis OCS observational clinical study, P prospectively collected data, R retrospectively collected data, D distal gastrectomy, P proximal gastrectomy, T total gastrectomy, PPG pylorus-preserving gastrectomy, B-I Billroth-I, B-II Billroth-II, R-Y Roux-en-Y, GG gastro-gastro anastomosis, E exclude, NR not reported Quality assessment based on the NOS for observational studies ①representativeness of exposed cohort ②selection of nonexposed cohort ③ascertainment of exposure ④outcome not present at the start of the study ⑤assessment of outcomes ⑥length of follow-up ⑦adequacy of follow-up

Intraoperative effects and postoperative recovery

As shown in Table 1, three studies did not report the information of conversion; two studies excluded the conversion cases, whereas another nine research studies had no conversion. The pooled data based on four studies, which reported conversion cases, showed similar conversion rates between groups (RR = 0.88, 95% CI: 0.36 ~ 2.17, P = 0.78). A longer operation time for RG than for LG was reported in the majority of research and meta-analysis revealed that the average operation time of LG was 49.05 min shorter than RG (WMD = −49.05 min; 95% CI: -58.18 ~ −39.91, P < 0.01) (Fig. 2a). Intraoperative EBL was reported in eighteen of the research studies, which was lower in RG than LG (WMD = 24.38 ml; 95% CI: 12.32 ~ 36.43, P < 0.01) (Fig. 2b).
Fig. 2

Forest plot of the meta-analysis for intraoperative effects and postoperative recovery. a Operation time. b Estimated blood loss. c Time to first flatus. d Time to restart oral intake. e Length of postoperative hospital stay

Forest plot of the meta-analysis for intraoperative effects and postoperative recovery. a Operation time. b Estimated blood loss. c Time to first flatus. d Time to restart oral intake. e Length of postoperative hospital stay The pooled mean time to first flatus indicated no significant difference between the two groups (WMD = 0.09 days; 95% CI: -0.10 ~ 0.27, P = 0.36) (Fig. 2c). Nonetheless, according to the meta-analysis, the mean time to restart oral intake was longer in LG than in RG (WMD = 0.23 days; 95% CI: 0.13 ~ 0.34, P < 0.01) (Fig. 2d). All studies reported the LOS. According to the pooled data, a significant difference did not exist between the two groups with regard to LOS (WMD = 0.35 days; 95% CI: -0.25 ~ 0.95, P = 0.25) (Fig. 2e). All intraoperative effects and postoperative recovery outcomes are summarized in Table 3.
Table 3

Results of the meta-analysis

OutcomesNo. of studiesSample sizeHeterogeneity (P, I 2)Overall effect size95% CI of overall effect P
LGRG
Conversion41660.68, 0%RR =0.880.36 ~ 2.170.78
Operation time (min)1941231830<0.001, 88%WMD = −49.05-58.18 ~ −39.91<0.01
Blood loss (mL)1840551762<0.001, 93%WMD =24.3812.32 ~ 36.43<0.01
Time to first flatus (days)91231713<0.001, 74%WMD =0.09-0.10 ~ 0.270.36
Time to oral intake (days)9205510960.67, 0%WMD =0.230.13 ~ 0.34<0.01
Hospital stay (days)1941231830<0.001, 82%WMD =0.35-0.25 ~ 0.950.25
Overall complications19412318300.82, 0%RR =0.960.82 ~ 1.130.65
Surgical complications17323415520.52, 0%RR =0.870.72 ~ 1.050.15
Medical complications1221379070.82, 0%RR =1.340.75 ~ 2.400.32
Reoperation717967890.35, 11%RR =0.690.29 ~ 1.620.39
Mortality721318380.91, 0%RR =0.670.26 ~ 1.740.41
Retrieved lymph nodes1732291585<0.001, 86%WMD = −1.44-3.26 ~ 0.370.12
Proximal margin (cm)9200610240.21, 26%WMD = −0.14-0.36 ~ 0.070.18
Distal margin (cm)81948973<0.001, 81%WMD =0.09-0.46 ~ 0.650.74
Recurrence35001870.39, 0%RR =1.090.57 ~ 2.050.80
Cost (USD)4390384<0.001, 93%WMD = −3944.8-4943.5 ~ −2946.2<0.01
Results of the meta-analysis

Morbidity and mortality

All studies reported adverse incidents ranging from 0% to 47.4% in RG and from 4.3% to 38.6% in LG. No significant difference in the rate of overall postoperative complications was identified between the groups of RG and LG (RR = 0.96, 95% CI: 0.82 ~ 1.13, P = 0.65) (Fig. 3a). Symmetry was shown in the visual inspection of the funnel plot, showing no severe publication bias (Fig. 4). After further analysis, surgical complications were similar between groups (RR = 0.87, 95% CI: 0.72 ~ 1.05, P = 0.15) (Fig. 3b), as were the medical complications (RR = 1.34, 95% CI: 0.75 ~ 2.40, P = 0.32) (Fig. 3c). Reoperation cases were reported in seven studies, and there was no significant difference in the reoperation rates (RR = 0.69, 95% CI: 0.29 ~ 1.62, P = 0.39) (Fig. 3d). Also, seven studies reported mortality and no significant difference could be found in postoperative mortality (RR = 0.67, 95% CI: 0.26 ~ 1.74, P = 0.41) (Fig. 3e). The specific reoperation and causes of mortality reported in the studies are summarized in Table 4. The meta-analysis results on morbidity and mortality are outlined in Table 3.
Fig. 3

Forest plot of the meta-analysis for morbidity and mortality. a Overall postoperative complications. b Surgical complications. c Medical complications. d Reoperation. e Mortality

Fig. 4

Funnel plot of the overall postoperative complications

Table 4

Systematic review of the specific reoperation and death reasons

AuthorGroupReoperationDeath
PuglieseLGEnterocutaneous leak (n = 1)Severe bleeding due to hepatic failure (n = 1)
RGNCHemorrhagic stroke (n = 1)
Kim KMLGLeak-related (n = 4)a Leak-related (n = 2)a
RGLeak-related (n = 6)a NC
RGLeakage and obstruction (n = 5)NC
LeeLGAnastomotic leakage (n = 1)NC
RGAnastomotic leakage (n = 1), anastomotic bleeding (n = 1)Anastomotic bleeding (n = 1)
HuangLGNCDuodenal stump leakage (n = 1)
RGNCGastrojejunostomy leakage (n = 1)
HanLGIntra-abdominal bleeding due to liver capsular injury (n = 1)NC
ParkLGNCImmediate postoperative bleeding (n = 1), mesenteric infarction (n = 1), septic shock caused by afferent loop syndrome (n = 1)
CianchiLGNCDuodenal stump leakage with peritonitis and sepsis (n = 1), acute myocardial infarction (n = 1)
RGIntestinal occlusion (n = 1)Cerebral vascular accident (n = 1)

NC no case

a: included anastomotic leakage and duodenal stump leakage

Forest plot of the meta-analysis for morbidity and mortality. a Overall postoperative complications. b Surgical complications. c Medical complications. d Reoperation. e Mortality Funnel plot of the overall postoperative complications Systematic review of the specific reoperation and death reasons NC no case a: included anastomotic leakage and duodenal stump leakage

Oncologic outcomes and long-term survival

The differences in the average number of RLNs were not considerable in the pooled statistics with a tendency towards a reduction in the LG group when compared to the RG group (WMD = −1.44; 95% CI: -3.26 ~ 0.37, P = 0.12) (Fig. 5a). The distal or proximal margin distances were described in nine studies. Meta-analysis of the proximal margin distances showed no significant difference between the two groups (WMD = −0.14 cm; 95% CI: -0.36 ~ 0.07, P = 0.18) (Fig. 5b), the same applies to the distal margin distance (WMD = 0.09 cm; 95% CI: -0.46 ~ 0.65, P = 0.74) (Fig. 5c). Cancer recurrence was reported in three research studies and the pooled data indicated that the difference between RG and LG was not significant (RR = 1.09, 95% CI: 0.57 ~ 2.05, P = 0.80). Long-term survival rates were reported in three research studies, and no considerable difference in the survival rates between the LG group and RG group could be found. In addition, during the follow-up time, no significant difference in the survival rates between both of the groups could be found in the studies of Lee et al. [34] and Han et al. [35] though they failed to report the particular survival rates. The meta-analysis of survival rates cannot be done due to the limited data. The systematic review outcomes of follow-up time, recurrence patterns and sites, and long-term survival rates are summarized in Table 5.
Fig. 5

Forest plot of the meta-analysis for oncologic outcomes. a Number of retrieved lymph nodes. b Proximal margin distances. c Distal margin distance. d Cancer recurrence

Table 5

Systematic Review of Recurrence and Long-term Survivals

AuthorGroupStageChemotherapyFollow-up (mo)RecurrenceSurvival (%)
PuglieseLGAny TNM0 T3 or any TN+ 53 (3–112)8a 3y–OS: 85; 5y–OS: 83&
RG28 (2–44)4a 3y–OS: 78&
Son TLGAny TNM0 NR703b 5y–DFS: 91.2; 5y–OS: 91.1
RG3b 5y–DFS: 90.2; 5y–OS: 89.5
ZhouLGAny TNM0 Routinely# 17(3–41)281, 2, 3-OS: 87.3, 77.1, 69.93y–OS N:82.6, 3y–OS N+:60.3
RG51, 2, 3-OS: 90.2, 78.1, 67.83y–OS N: 84.4, 3y–OS N+: 57.5
LeeLGAny TNM0 NR75NRNSD
RG
HanLGcT1-2N0M0 3 cases (4.4%)$ 19.30NSD
RG3 cases (4.4%)$ 22.70

Follow-up time were shown as median (range) or median only

DFS disease-free survival, OS overall survival, y year, N − negative nodal metastasis, N positive nodal metastasis, NR not report, NSD only reported no significant difference between two groups without specific survival rate

asome patients had mixed tumor recurrence, identified recurrence in LG: local (n = 2), peritoneum (n = 2), liver (n = 1), lung (n = 2), bone (n = 1); identified recurrence in RG: peritoneum (n = 1), liver (n = 1), bone (n = 1). &: for overall patients, 5y–OS N−: 97%, 5y–OS N+: 52%

bLG, peritoneum (n = 2), lung (n = 1); RG, breast (n = 1), splenic hilum (n = 1), ovary (n = 1). #: 5-fluorouracil + oxaliplatin intravenous chemotherapy. $: because of advanced disease status after surgery

Forest plot of the meta-analysis for oncologic outcomes. a Number of retrieved lymph nodes. b Proximal margin distances. c Distal margin distance. d Cancer recurrence Systematic Review of Recurrence and Long-term Survivals Follow-up time were shown as median (range) or median only DFS disease-free survival, OS overall survival, y year, N − negative nodal metastasis, N positive nodal metastasis, NR not report, NSD only reported no significant difference between two groups without specific survival rate asome patients had mixed tumor recurrence, identified recurrence in LG: local (n = 2), peritoneum (n = 2), liver (n = 1), lung (n = 2), bone (n = 1); identified recurrence in RG: peritoneum (n = 1), liver (n = 1), bone (n = 1). &: for overall patients, 5y–OS N−: 97%, 5y–OS N+: 52% bLG, peritoneum (n = 2), lung (n = 1); RG, breast (n = 1), splenic hilum (n = 1), ovary (n = 1). #: 5-fluorouracil + oxaliplatin intravenous chemotherapy. $: because of advanced disease status after surgery

Total cost

Only four studies recorded their total cost and they all reported a higher cost for RG than LG. The meta-analysis demonstrated that the total cost of RG groups was significantly higher than LG groups (WMD = −3944.8 USD; 95% CI: -4943.5 ~ −2946.2, P < 0.01) (Fig. 6).
Fig. 6

Forest plot of the meta-analysis for total cost

Forest plot of the meta-analysis for total cost

Subgroup analysis of distal or total gastrectomy

For the subgroup analysis of distal gastrectomy (DG), the RG group still holds the longer operation time (P < 0.01), lower EBL (P < 0.05) and with similar LOS, overall complications, mortality as well as RLN (P > 0.05). However, there was a reduced time to oral intake for RG, but with only a marginal difference compared to the LG group (P = 0.05). As for total gastrectomy (TG), there is no large difference between the outcomes of operation time, EBL, time to oral intake, LOS, overall complications and mortality against DG subgroup analysis, the number of RLNs of RG was more than that of LG with a significant difference (P = 0.03). The subgroup analysis results of surgical extension are summarized in Table 6. Generally speaking, the difference in surgical extension had little effect on the overall meta-analysis results.
Table 6

Results of the subgroup analysis of distal or total gastrectomy

OutcomesNo. of studiesSample sizeHeterogeneity (P, I 2)Overall effect size95% CI of overall effect P
LGRG
Operation time (min)
 DG81635453<0.001, 78%WMD = −57.08−68.62 ~ −45.54<0.01
 TG54481660.004, 74%WMD = −42.62−66.72 ~ −18.52<0.01
Blood loss (mL)
 DG81635453<0.001, 77%WMD =19.273.86 ~ 34.680.01
 TG54481660.54, 0%WMD =23.771.97 ~ 45.560.03
Time to oral intake (days)
 DG33441160.49, 0%WMD =0.180.00 ~ 0.360.05
 TG32511000.71, 0%WMD = −0.18−0.55 ~ 0.200.36
Hospital stay (days)
 DG81635453<0.001, 92%WMD =0.52−0.69 ~ 1.740.40
 TG54481660.75, 0%WMD =0.28−0.80 ~ 1.360.61
Overall complications
 DG816354530.86, 0%RR =1.190.83 ~ 1.710.34
 TG43301400.49, 0%RR =1.320.80 ~ 2.180.27
Mortality
 DG49422130.84, 0%RR =0.840.21 ~ 3.300.80
 TG2194810.55, 0%RR =0.150.02 ~ 1.410.10
Retrieved lymph nodes
 DG81635453<0.001, 92%WMD = −2.10−5.90 ~ 1.700.28
 TG54481660.63, 0%WMD = −2.51−4.83 ~ −0.190.03

DG distal gastrectomy, TG total gastrectomy

Results of the subgroup analysis of distal or total gastrectomy DG distal gastrectomy, TG total gastrectomy

Subgroup analysis of weight influence

Only two studies had data for subgroup analysis based on weight [28, 34]. The patients were divided based on preoperative BMI into non-overweight (BMI < 25 kg/m2) and overweight (BMI >25 kg/m2) groups. In the non-overweight subgroup, the RG group still had a longer operation time (P < 0.01), while in the overweight subgroup; the operation time was similar between groups (P = 0.27). In addition, there was no significant difference between LG and RG for the outcomes of EBL and RLNs regardless of overweight or non-overweight subgroup. Other perioperative outcomes cannot be analyzed due to the limited data. The subgroup analysis results based on weight are summarized in Table 7.
Table 7

Results of the subgroup analysis of weight

OutcomesNo. of studiesSample sizeHeterogeneity (P, I 2)Overall effect size95% CI of overall effect P
LGRG
Operation time (min)
 non-overweight22321270.06, 72%WMD = −37.63−62.82 ~ −12.43<0.01
 overweight2118440.008, 86%WMD = −28.58−79.11 ~ 21.940.27
Blood loss (mL)
 non-overweight22321270.11, 60%WMD =0.90−13.44 ~ 15.250.90
 overweight2118440.03, 80%WMD =39.84−41.71 ~ 121.390.34
Retrieved lymph nodes
 non-overweight22321270.34, 0%WMD = −1.88−4.78 ~ 1.010.20
 overweight2118440.03, 79%WMD =4.32−4.10 ~ 12.740.31
Results of the subgroup analysis of weight

Discussion

The cost-effectiveness and definite advantages of RG have not been well documented, which is different when compared to the evolution of LG versus conventional open surgery [20]. However, the number of publications on RG has gradually increased in recent years. The oncologic outcomes, postoperative outcome, intraoperative effects and costs of a total of 1830 patients who underwent RG for gastric cancer treatment in 19 studies were reviewed as we believe such research would contribute to a more objective and comprehensive assessment of the current RG surgical status. In spite of the considerable heterogeneity, the prolonged operating time in RG was shown in almost all the included research studies. The prolonged exposure time to pneumoperitoneum and the associated increased time of anesthesia is a major concern. Few publications describe the effect of longer operation times during RG. However, previous research of LG in senior patients has shown that longer operation time did not result in detrimental effects with regard to surgical results [41]. Therefore, a prolonged operating time should not affect surgeons directly on conducting research on RG’s new utility. Inevitably, the docking time was considered as an essential factor, which enhanced the operating time. The docking time was between 20 min to 60 min as reported in our study [7, 13, 15, 31], We found RG had longer operation times than LG by 49 min, which suggested the ‘true’ time spent on operations was similar or even shorter than LG. Furthermore, with the increased utilization of the new robotic surgical system, operation times are expected to shorten. Several studies have reported that the da Vinci Xi robotic platform is more user-friendly and is easier to install in rectal and nephritic surgery [42, 43]. As a result, we believed that RG is technically feasible with regard to operation time. Surgeons have to go through a learning curve to master a technique. The surgical results, such as operation time, oncological outcomes and postoperative complications can be affected by surgeon’s familiarity with the instrument, experience and assistant compliance. In general, before stabilization, LG should be conducted on around 40 to 60 cases [44]. The learning curve for RG was shorter for experienced surgeon who had performed LG, which is forecasted to be only 10 to 20 cases [12, 13, 18, 26]. A surgeon experienced in laparoscopic surgery can conduct robotic surgery securely even in their first case [16]. Several studies investigated in this meta-analysis compared the initial and later experiences of robotic surgery [12, 13, 18, 26]. The later cases performed by the same surgical team could progress toward shortening operation times. Postoperative morbidity is the main indicator for assessing the safety and feasibility of one procedure. It is widely accepted that laparoscopic surgery for gastric cancer is safer and could have fewer complications than open surgery [45]. Our meta-analysis demonstrated a comparable complication rate in RG versus LG group, and the low heterogeneity regardless of overall, surgical or medical complications encourages us to believe that RG indeed is as safe as LG. Improvements such as three-dimension images and tremor filtering could theoretically contribute to safer implementations of the robotic system for gastrectomy and lymphadenectomy. According to the multivariate analyses in the Suda study, the application of RG was an important independent protective factor in regards to the postoperative complication [37]. Tokunaga et al. [46, 47] reported the incidences of overall adverse events after RG which were 14.2% and 22.2% based on their two-phase II studies, which are comparable to the rates of 19–27% in previous studies of LG [48, 49]. Obesity is one of the most significant health problems today and rates are still increasing around the world. Some studies claim obesity causes increased blood loss, operation time, and wound infection rate et al. [50, 51], whereas others did not observe any negative effect on surgical outcomes [52]. Recently, Harr et al. [10] showed that the benefits of robotic methods were more evident in high versus normal BMI patients when performing a colostomy. The authors concluded that robotic surgery might overcome the difficulties associated with thick abdominal walls and excessive intra-abdominal fat, thanks to improved visualization, instrumentation, and ergonomics [10]. However, compared to other operations such as the colorectal or prostatic surgeries, which are in relatively narrow regions, the superiority of da Vinci over the laparoscopy may not be obvious, in that gastric surgery is conducted in the upper abdomen of a relatively spacious location. In our study, the overall mean operation time of RG and LG were similar in the overweight subgroups, contrasting with those in the non-overweight subgroups, which implied RG to be superior to LG when used on overweight patients. However, the sample size of the overweight subgroups was not large enough to be conclusive. The traditional straight forceps in LG fail to enable surgeons to reach deep-seated vessels and other areas, like the supra pancreatic one, in which the dissection of lymph nodes around the splenic hilum, splenic artery, and hepatic artery areas is deemed extremely hard. The tremor filtering, wristed instruments, as well as stable exposure and high-solution image can help surgeons thoroughly retrieve the lymph nodes around the delicate areas [21]. According to one included study, the amount of RLNs was considerably higher with robotic surgery in the splenic hilum and splenic artery areas [29]. Our meta-analysis shows adequate RLNs with means of 35.4 and 36.1 in the LG and RG groups, respectively. The mean number of RLNs of RG was more than that of LG with a marginal difference observed in the pooled data, even though most studies had been done during initial implementation of the robotic technique. Therefore, we believe that robotic technique could be superior to the conventional laparoscopic technique for lymphadenectomy. Since the history of the clinical application of RG is a short one, few reports have compared long-term survival outcomes with other methods. Coratti et al. [53] demonstrated that the 5-year survival rate after RG stratified with Stage IA, IB, II, and III was 100%, 84.6%, 76.9%, and 21.5%, respectively. Pugliese et al. [11] reported a cumulative overall 5-year survival rate of 78% with a mean follow up of 30 months (range 2–86) after RG for gastric cancer. The application of robotic surgery remains controversial, mainly due to the considerable expense. The total difference in cost between the LG and RG groups has been predicted to be around 3900 USD [18, 31, 38], which is mainly derived from the robotic system itself. According to the opinions of some investigators, the higher cost of robotic surgery is not enough to justify the theoretical advantages of this technology [54]. If RG can reduce complications and shorten hospital stay, the higher costs of the robotic system would be partially offset. Based on this, it is essential for robotic operators to inspect whether the potential advantages of the robotic approach justifies its high cost in the treatment of gastric cancer. Our research has the following limitations: (1) Selection bias: As no RCT was available to be included in the meta-analysis due to the higher cost of robotic surgery, selection biases are inevitable in surgical abstention which should be carefully interpreted. (2) Clinical heterogeneity: The homogeneity test for the continuous variables exhibited substantial heterogeneity due to the inherent flaws of a retrospective study, the uneven surgical skills of the different surgeons, as well as regional differences, etc. More importantly, for surgeons in the East, radical distal gastrectomy for middle and distal gastric cancer is popular [55], while the distal subtotal is preferred in the West [56]. Thus we cataloged distal gastrectomy and subtotal gastrectomy as a subgroup. Though it brings some interesting results due to the expansion of sample size, such a combination would result in clinical heterogeneity. (3) Regional difference: The majority of the included studies came from East Asia, because East Asia has the highest prevalence of gastric cancer, while gastric cancer is relatively uncommon in Western countries. Besides, in East Asia, particularly Korea, Japan and some areas of China, the proportion of early gastric cancer has increased as a result of the improved surveillance of gastric cancer in these regions [57, 58]. On the other hand, although increasing evidence continues to show no difference between patients undergoing open or laparoscopic surgery for oncologic outcomes, the Japanese Gastric Cancer Association still classifies minimal invasive surgery as investigational treatment and only recommends minimal invasive surgery for early stage gastric cancer patients [55]. Therefore, the cases in our studies, especially those from East Asia, were mainly early stage cases. All of the above limitations must be kept in mind when interpreting the results of our study.

Conclusions

Except for the longer operation time and higher costs, RG for the patients with gastric cancer was not inferior to LG. Besides; RG holds the potential benefits for larger numbers of lymph node dissection and reduced intraoperative blood loss. Further prospective studies are needed in order to confirm these advantages. In addition, long-term results are needed, particularly for the oncological adequacy of robotic gastric cancer resections.
  57 in total

1.  Comparison of Surgical Outcomes of Robot-Assisted and Laparoscopy-Assisted Pylorus-Preserving Gastrectomy for Gastric Cancer: A Propensity Score Matching Analysis.

Authors:  Dong-Seok Han; Yun-Suhk Suh; Hye Seong Ahn; Seong-Ho Kong; Hyuk-Joon Lee; Woo-Ho Kim; Han-Kwang Yang
Journal:  Ann Surg Oncol       Date:  2014-11-01       Impact factor: 5.344

2.  Robot-assisted gastrectomy with lymph node dissection for gastric cancer: lessons learned from an initial 100 consecutive procedures.

Authors:  Jyewon Song; Sung Jin Oh; Wook Ho Kang; Woo Jin Hyung; Seung Ho Choi; Sung Hoon Noh
Journal:  Ann Surg       Date:  2009-06       Impact factor: 12.969

3.  [Comparative study on da Vince robotic and laparoscopic radical gastrectomy for gastric cancer].

Authors:  Jiang Liu; Hu Ruan; Kun Zhao; Gang Wang; Min Li; Zhiwei Jiang
Journal:  Zhonghua Wei Chang Wai Ke Za Zhi       Date:  2014-05

4.  Laparoscopic versus open distal gastrectomy for gastric cancer: a meta-analysis of randomized controlled trials and high-quality nonrandomized studies.

Authors:  Eduardo F Viñuela; Mithat Gonen; Murray F Brennan; Daniel G Coit; Vivian E Strong
Journal:  Ann Surg       Date:  2012-03       Impact factor: 12.969

5.  Major early complications following open, laparoscopic and robotic gastrectomy.

Authors:  K M Kim; J Y An; H I Kim; J H Cheong; W J Hyung; S H Noh
Journal:  Br J Surg       Date:  2012-10-03       Impact factor: 6.939

Review 6.  Comparison of short-term surgical outcomes between totally laparoscopic and laparoscopic-assisted distal gastrectomy for gastric cancer: a 10-y single-center experience with meta-analysis.

Authors:  Ke Chen; Yi-Ping Mou; Xiao-Wu Xu; Yu Pan; Yu-Cheng Zhou; Jia-Qin Cai; Chao-Jie Huang
Journal:  J Surg Res       Date:  2014-10-22       Impact factor: 2.192

7.  Outcomes and survival after laparoscopic gastrectomy for adenocarcinoma. Analysis on 65 patients operated on by conventional or robot-assisted minimal access procedures.

Authors:  R Pugliese; D Maggioni; F Sansonna; G C Ferrari; A Forgione; A Costanzi; C Magistro; J Pauna; S Di Lernia; D Citterio; C Brambilla
Journal:  Eur J Surg Oncol       Date:  2008-03-14       Impact factor: 4.424

8.  Use of the new da Vinci Xi® during robotic rectal resection for cancer: a pilot matched-case comparison with the da Vinci Si®.

Authors:  Luca Morelli; Simone Guadagni; Gregorio Di Franco; Matteo Palmeri; Giovanni Caprili; Cristiano D'Isidoro; Luigi Cobuccio; Emanuele Marciano; Giulio Di Candio; Franco Mosca
Journal:  Int J Med Robot       Date:  2016-01-25       Impact factor: 2.547

9.  Clinicopathological features and surgical treatment of gastric cancer in South Korea: the results of 2009 nationwide survey on surgically treated gastric cancer patients.

Authors:  Oh Jeong; Young-Kyu Park
Journal:  J Gastric Cancer       Date:  2011-06-30       Impact factor: 3.720

10.  Comparison of the operative outcomes and learning curves between laparoscopic and robotic gastrectomy for gastric cancer.

Authors:  Kuo-Hung Huang; Yuan-Tzu Lan; Wen-Liang Fang; Jen-Hao Chen; Su-Shun Lo; Anna Fen-Yau Li; Shih-Hwa Chiou; Chew-Wun Wu; Yi-Ming Shyr
Journal:  PLoS One       Date:  2014-10-31       Impact factor: 3.240

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  28 in total

1.  What are the reasons for a longer operation time in robotic gastrectomy than in laparoscopic gastrectomy for stomach cancer?

Authors:  Heli Liu; Takahiro Kinoshita; Akiko Tonouchi; Akio Kaito; Masanori Tokunaga
Journal:  Surg Endosc       Date:  2018-06-25       Impact factor: 4.584

Review 2.  Clinical efficacy and safety of robotic distal gastrectomy for gastric cancer: a systematic review and meta-analysis.

Authors:  Shiyi Gong; Xiong Li; Hongwei Tian; Shaoming Song; Tingting Lu; Wutang Jing; Xianbin Huang; Yongcheng Xu; Xingqiang Wang; Kaixuan Zhao; Kehu Yang; Tiankang Guo
Journal:  Surg Endosc       Date:  2022-01-12       Impact factor: 4.584

3.  Effectiveness and safety of robotic gastrectomy versus laparoscopic gastrectomy for gastric cancer: a meta-analysis of 12,401 gastric cancer patients.

Authors:  Tao Jin; Han-Dong Liu; Kun Yang; Ze-Hua Chen; Yue-Xin Zhang; Jian-Kun Hu
Journal:  Updates Surg       Date:  2021-10-16

4.  Comparison of robotic gastrectomy and laparoscopic gastrectomy for gastric cancer: a propensity score-matched analysis.

Authors:  Takeshi Omori; Kazuyoshi Yamamoto; Hisashi Hara; Naoki Shinno; Masaaki Yamamoto; Kohei Fujita; Takashi Kanemura; Tomohira Takeoka; Hirofumi Akita; Hiroshi Wada; Masayoshi Yasui; Chu Matsuda; Junichi Nishimura; Yoshiyuki Fujiwara; Hiroshi Miyata; Masayuki Ohue; Masato Sakon
Journal:  Surg Endosc       Date:  2022-02-28       Impact factor: 3.453

5.  Robotic versus laparoscopic gastrectomy with lymph node dissection for gastric cancer: study protocol for a randomized controlled trial.

Authors:  Toshiyasu Ojima; Masaki Nakamura; Mikihito Nakamori; Keiji Hayata; Masahiro Katsuda; Junya Kitadani; Shimpei Maruoka; Toshio Shimokawa; Hiroki Yamaue
Journal:  Trials       Date:  2018-07-31       Impact factor: 2.279

6.  Short-term outcomes of robotic- versus laparoscopic-assisted Total Gastrectomy for advanced gastric Cancer: a propensity score matching study.

Authors:  Changdong Yang; Yan Shi; Shaohui Xie; Jun Chen; Yongliang Zhao; Feng Qian; Yingxue Hao; Bo Tang; Peiwu Yu
Journal:  BMC Cancer       Date:  2020-07-17       Impact factor: 4.430

7.  Comparison of short-term surgical outcomes using da Vinci S, Si and Xi Surgical System for robotic gastric cancer surgery.

Authors:  Toshiyasu Ojima; Masaki Nakamura; Keiji Hayata; Junya Kitadani; Akihiro Takeuchi; Hiroki Yamaue
Journal:  Sci Rep       Date:  2021-05-26       Impact factor: 4.379

Review 8.  The 140 years' journey of gastric cancer surgery: From the two hands of Billroth to the multiple hands of the robot.

Authors:  Masanori Terashima
Journal:  Ann Gastroenterol Surg       Date:  2021-02-12

9.  Robotic versus laparoscopic gastrectomy with D2 lymph node dissection for advanced gastric cancer: a propensity score-matched analysis.

Authors:  Zhengyan Li; Jipeng Li; Bofei Li; Bin Bai; Yezhou Liu; Bo Lian; Qingchuan Zhao
Journal:  Cancer Manag Res       Date:  2018-04-10       Impact factor: 3.989

Review 10.  Between evidence and new perspectives on the current state of the multimodal approach to gastric cancer: Is there still a role for radiation therapy?

Authors:  Linda Agolli; Luca Nicosia
Journal:  World J Gastrointest Oncol       Date:  2018-09-15
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