- Research article
- Open Access
A meta-analysis of comparison of proximal gastrectomy with double-tract reconstruction and total gastrectomy for proximal early gastric cancer
BMC Surgery volume 19, Article number: 117 (2019)
In theory, proximal gastrectomy with double-tract reconstruction (PG-DT) was superior to total gastrectomy (TG) in hematologic and nutritional outcomes. However, its clinical effects in proximal early gastric cancer (EGC) have been controversial.
The purpose of this study was to investigate the outcomes of laparoscopic proximal gastrectomy with double-tract reconstruction (LPG-DT) for proximal EGC. For this systematic review and meta-analysis, we searched for articles published before December of 2018 in the following databases: PubMed, Web of Science, EBSCO, Medline, and Cochrane Library.
The results showed no significant difference in the anastomotic stenosis (OR = 0.91, 95%CI = 0.33–2.50, p = 0.85) and reflux esophagitis (OR = 1.87, 95%CI = 0.62–5.65, p = 0.27) between LPG-DT and laparoscopic total gastrectomy (LTG). The vitamin B12 supplementation rate in the LPG-DT group was lower than the LTG group (OR = 0.06, 95%Cl = 0.01–0.59, p = 0.02).
Due to comparable clinical effect, PG-DT is comparable to TG for patients with proximal EGC. In addition, LPG-DT not only appears superior to TG in terms of preventing vitamin B12 deficiency, but also does not increase the risk of anastomotic stricture and reflux esophagitis.
Recently, with the prevalence of endoscopic techniques, the incidence of proximal gastric cancer (lesion located in the upper third of the stomach), especially proximal early gastric cancer (EGC) has been increasing in worldwide . So far, for patients with proximal EGC who have lesions unsuitable for endoscopic treatment, total gastrectomy (TG) is the most major surgical procedure for the radical treatment. However, TG has many potential disadvantages, especially in hematological and nutritional status . Thus, some researchers have suggested the proximal gastrectomy (PG) as an alternative to TG for proximal EGC . Unfortunately, severe reflux esophagitis and anastomotic stenosis are the major factors that limit the clinical application of this surgery. Besides, the operation procedure needs to be further standardized [4, 5].
Some scholars suggested that patients with proximal EGC could be treated with proximal gastrectomy with double-tract reconstruction (PG-DT), to avoid anastomotic complications [6, 7]. It was reported that the incidences of reflux symptoms, usage of proton pump inhibitors, and anastomotic strictures were significantly lower in the double-tract anastomosis group as compared to the esophagogastrostomy group . However, a recent multicenter study from the western experience showed that patients who underwent PG have an increased mortality rate and a higher risk of reflux esophagitis and anastomotic stricture .
In addition, in view of the prognosis of EGC is excellent, the improvement of postoperative quality of life and the safe application of minimally invasive surgery have become the research hotspot in recent years. There is no doubt that laparoscopic proximal gastrectomy (LPG) is one of the most promising treatments for patients with proximal EGC . But LPG has remained controversial mainly due to a lack of evidence from large-scale studies. And there were few meta-analyses about this problem in comparison of laparoscopic proximal gastrectomy with double-tract reconstruction (LPG-DT) and laparoscopic total gastrectomy (LTG) for treatment effects. So, this meta-analysis is a comparison of the short-term and long-term outcomes of LPG-DT and LTG for proximal EGC through comprehensive retrieval and pooled analysis.
In the electronic databases of PubMed, Web of science, EBSCO and the Cochrane library, a comprehensive literature search strategy was performed by retrieving the keywords “proximal gastrectomy” and “total gastrectomy” until December 2018. To avoid omitting any potential studies, we manually reviewed the references of included literature. Non-English studies will be excluded. Institutional review board approval of our hospital was obtained for this study.
Two authors individually conducted the search and independently reviewed and extracted data from each study. The search results were compared, and any disagreement in opinions were resolved by further discussion. This meta-analysis included studies that met the following criteria: (1) studies focusing on patients with early gastric cancer; (2) comparative studies between PG-DT and TG; (3) having reported detailed/available data of the surgical results, including short- and/or long-term outcomes. But these studies were excluded if they were (1) non-original articles; (2) not comparing PG-DT and TG; (3) not relevant outcome or detailed data.
Data extracted included study characteristics (such as author, region, study period, design, case number), patient demographics (such as age, gender, body mass index), tumor stage, surgical results (such as operation time, the number of retrieved lymph nodes, perioperative complication and resection margin), long-term outcomes (hematological and nutritional outcomes), and oncological outcome. Corresponding authors were contacted if further information was needed.
Evaluation of quality of the studies
This meta-analysis was conducted on the recommendation of guidelines of the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) 2009 Checklist (Additional file 1: Table S1) . Two authors independently assessed the quality of the included researches, according to the Newcastle-Ottawa Quality Assessment Scale (NOS) checklist, which consisted of eight items, divided into three aspects (selection, comparability and outcome) with a maximum number of 9 stars .
RevMan 5.3.5 software for Windows® was used to analyze the data. According to data characteristics, dichotomous variables and continuous variables were pooled analyzed using estimation of odds ratios (OR) and weighted mean difference (WMD) with a 95% Confidence interval (CI), respectively. Heterogeneity across studies was evaluated by Cochrane Q-test and p-values. We considered heterogeneity to be present if the p < 0.1. The fixed-effect model was used for meta-analysis in cases of nonsignificant heterogeneity. On the contrary, if there was a significant heterogeneity, the random-effect model was used. Publication bias was evaluated by Egger’s test. Egger’s test was not suitable for subgroup analysis, if less than ten studies were included due to low sensitivity of qualitative and quantitative tests. All statistical tests were performed two-sided, and p < 0.05 was considered statistically significant.
A total of 1451 studies were identified after the initial search. After deletion of 631 duplicates, 771 studies were additionally excluded by careful review of the title and/or abstract. After screening the title and abstract, 49 studies were evaluated via full-text articles. At last, seven articles [7, 12,13,14,15,16,17] published were included for quantitative synthesis from 2016 to 2018. The flow diagram were summarized is shown in Fig. 1.
Based on the inclusion and exclusion criteria, seven retrospective studies were included for this review. The characteristics of each study were shown in Table 1. The seven studies included a total of 592 patients: PG-DT was performed in 347 patients and TG was performed in 245 patients. The sample size of each study varied from 30 to 248 patients. All patients received laparoscopic or robotic surgery, of which 533 cases (90.0%) of belonged to stage I proximal gastric cancer. In the PG-DT group, 331 patients (95.4%) were stage I proximal gastric cancer, and in the TG group, 202 cases (82.4%) were stage I proximal gastric cancer.
Patient’s clinicopathologic features
In the analysis of patients’ basic conditions, there were differences in gender (OR = 1.89,95% CI = 1.26–2.84, p = 0.002, fixed-effects model) and American Society of Anesthesiologist (ASA) (OR = 0.43, 95%CI = 0.22–0.83, p = 0.01, fixed-effects model) between both groups of patients underwent surgical treatment (LPG-DT vs. LTG). In terms of tumor lesion, patients with LPG-DT had smaller tumor sizes than those with LTG (WMD = -0.94, 95%CI = -1.26-(− 0.62), p < 0.001, fixed-effects model). The T stage (OR = 2.21, 95% CI = 1.17–4.17, p = 0.01, fixed-effects model) and tumor stage (OR = 2.70, 95%CI = 1.35–5.39, p = 0.005, fixed-effects model) were earlier in the LPG-DT group. However, there was no significant difference in N Stage between both groups (OR = 0.77, 95%CI = 0.34–1.71, p = 0.52, fixed-effects model) (Table 2).
Surgical conditions and short-term outcomes
In terms of surgical conditions, patients in the LTG group had longer proximal (WMD = -0.97, 95%CI = -1.80-(− 0.14), p = 0.02, random-effects model) and distal resection margins (WMD = -8.30, 95%CI = -9.57-(− 7.03), p < 0.001, random-effects model) and more retrieved lymph nodes (WMD = -11.28, 95%CI = -13.52-(− 9.04), p < 0.001, fixed-effects model). However, there was no significant difference in operative time (WMD = -10.43, 95%CI = -25.64–4.77, p = 0.18, random-effects model) and intraoperative blood loss (WMD = 3.74, 95%CI = − 57.37-64.84, p = 0.90, random-effects model) between both groups (Table 2).
Besides, there was no significant difference in short-term outcomes between both groups, including postoperative the length of hospital stay (WMD = -0.21, 95%CI = -1.21–0.80, p = 0.68, fixed-effects model), all complications (Clavien-Dindo Grade I or more) (OR = 0.87, 95%CI = 0.36–2.13, p = 0.76, random-effects model), severe complications (Clavien-Dindo Grade III or more) (OR = 0.35, 95%CI = 0.12–1.07, p = 0.07, fixed-effects model), and anastomotic leakage (OR = 0.81, 95%CI = 0.34–1.94, p = 0.64, fixed-effects model) (Table 2).
The long-term results including anastomotic stenosis, reflux, hematological status, vitamin B12, and oncological outcomes were analyzed. There was also no statistically significant difference between anastomotic stenosis (OR = 0.91, 95%CI = 0.33–2.50, p = 0.85, fixed-effects model) and reflux (OR = 1.87, 95%CI = 0.62–5.65, p = 0.27, fixed-effects model) (Fig. 2). By comparing the hematological and nutritional outcomes between both groups, body mass index (BMI) was mentioned in five studies, among which three showed statistical difference and two showed no statistical difference. Hemoglobin was investigated in six studies, among which only one showed statistical difference, while the other five showed no statistical difference. Ferritin was mentioned in two studies, they all showed no statistical difference. In addition, there were many studies investigated total protein, albumin, total cholesterol and total lymphocyte count, none of the results were statistically significant (Additional file 2: Table S2). Four of these studies reported postoperative vitamin B12. The vitamin B12 supplementation rate in the LPG-DT group was lower than the LTG group (OR = 0.06, 95%Cl = 0.01–0.59, p = 0.02, random-effects model) (Fig. 2). At the end of follow-up, no patients underwent LPG-DT had recurrence or death. In the LTG group, a total of 4 patients relapsed.
PG is theoretically the ideal treatment option for proximal EGC . However, the risk of reflux esophagitis and anastomotic stenosis is a huge challenge for the widespread use of PG. To improvement these disadvantages, several modified reconstruction procedures, including jejunal interposition, jejunal pounch interposition, double-flap, and double-tract anastomosis, have been attempted [6, 19,20,21]. According to previous studies, PG-DT is one of the most promising procedures, in reducing anastomotic complications (reflux esophagitis and anastomotic stenosis) and improving operative quality of life [7, 12]. Thus, the purpose of this meta-analysis is to compare the safety and feasibility of LPG-DT with LTG for patients with clinical stage I proximal gastric cancer.
In this study, the tumor size of the LTG group was significantly larger than that of the LPG-DT group. Although tumor depth and tumor staging was significantly earlier in the LPG-DT group than in the LTG group, there was no difference in lymph node metastasis. It seems that the size and depth of the tumor are factors in the choice of surgical procedure. Masuzawa et al.  reported that tumor size and histology could influence the size of the remnant stomach, which was an important factor in choosing the procedure. So, we believed that LPG-DT was appropriate for proximal EGC, and the tumor size was small. In terms of operation time and blood loss, no significant difference was found between the two groups. Thus, LPG-DT is not a complicated procedure, compared LTG. Although resection margins were shorter for LPG-DT, intraoperative frozen biopsies confirm disease-free resection margins (R0 resection). In other words, PG can maximize the retention of gastric stump. In addition, consistent with previous findings [20, 23], this study showed that fewer lymph nodes were retrieved every patient in the LPG-DT group because of different lymph node metastasis dissection extent. The TNM staging system recommends that no less than 16 lymph nodes should be resected for radical gastrectomy . And several studies have shown that the number of lymph nodes retrieved is closely associated with postoperative pathologic staging and prognostic assessment [24, 25]. Gholami et al. . demonstrated that dissection of 16 or more lymph nodes was associated with better survival in all patients. However, some studies suggested that dissection of more than 16 LNs did not show improvement in the prognosis in stage I patients [27, 28]. In our previous study , there was a low incidence of lymph node metastasis in EGC. So, we believed that LPG-DT with less than D2 lymph node dissection appears to be reasonable.
An et al.  and Rosa et al.  reported that PG with esophagogastrostomy resulted in a higher complication rate than TG and that PG with esophagogastrostomy led to a higher frequency of stenosis and reflux than did TG. Nishigori et al.  also demonstrated that PG with esophagogastrostomy had a higher probability of anastomotic stenosis. There was no significant difference in the short-term outcomes between the two groups (LPG-DT versus LTG) in this article. Whether in all complications or severe complications, the present study showed that LPG-DT was a feasible and safe technique. Most importantly, the results of this study showed that LPG-DT did not increase the incidences of reflux esophagitis and anastomotic stenosis, compared LTG. Besides, Aburatani et al.  suggested that the incidence of both reflux esophagitis and anastomotic stenosis was lower in the PG-DT group than in the PG with esophagogastrostomy group. We could conclude that LPG-DT was a good alternative to LTG, because of similar complication rate.
There is no doubt that the long-term quality of life is one of the important factors to evaluate the value of surgery, especially for patients with EGC. Several previous studies had reported hematological and nutritional outcomes in patients underwent PG. Cho et al.  reported that postoperative hematologic indexes, including hemoglobin, ferritin, transferrin saturation, and anemia, showed no significant difference between minimally invasive PG-DT and minimally invasive TG. Protein, albumin, cholesterol, and other nutritional parameters were also comparable between the two groups. They also concluded that although the proportion of patients who requiring vitamin B12 supplements was smaller in the PG-DT group, the cumulative incidence of vitamin B12 deficiency after PG-DT was similar to that after TG. Jung et al.  thought that the change rate of body weight in LPG-DT group was significantly lower than in LTG group. The serum vitamin B12 level in the LPG-DT group was significantly higher than in the LTG group. Research by Kim and his colleagues  observed that LPG-DT was beneficial with regards to the absorption of iron and vitamin B12 compared to LTG. A recent study has shown that body weight and skeletal muscle index reduction rates were lower in the LPG-DT group than in the LTG group .
In this present study, a significantly smaller proportion of the LPG-DT patients required vitamin B12 supplementation compared to the LTG group. PG-DT preserves the gastric antrum and part of the gastric body, allowing for food reserve, which indicates that these areas of the stomach are potential sources of intrinsic factors. TG is known to have a risk of leading to vitamin B12 deficiency compared to distal gastrectomy . Because the main source of intrinsic factors in the stomach is parietal cells, which are mainly located in the body and fundus, the ability of PG to prevent vitamin B12 deficiency is questionable. Our analysis showed that retention of the distal stomach assists in the absorption of the vitamin B12, possibly due to retention of a partial gastric body.
This systematic review and meta-analysis incorporated seven articles that compared the long-term hematological and nutritional indicators, including postoperative BMI, hemoglobin, ferritin, total protein, albumin, to patients with LPG-DT and LTG. Unfortunately, the analysis of forest plots with related indicators could not be obtained due to the inability to obtain the original data. However, no study showed that the hematological and nutritional status of patients who underwent LPG-DT was worse than that of patients underwent LTG.
Finally, in terms of oncology prognosis, the two groups had similar outcomes. Yoo et al.  reported that PG might increase the likelihood of local recurrence, although it would not affect long-terms in terms of survival and mortality. But the study included many patients with advanced gastric cancer. In this study, almost all the patients included had EGC. There was no recurrence or death in the patients with confirmed stage I proximal gastric cancer after LPG-DT. Therefore, we believed that LPG did not negatively influence the prognosis compared to LTG in EGC.
To our knowledge, this is the first meta-analysis investigates the short-term and long-term results of LPG-DT versus LTG. Some limitations of this study need to be emphasized. All included articles were the small sample retrospective studies, which inevitably led to a decline in the level of evidence in this paper. No prospective studies or clinical trials were found through systematic and comprehensive retrieval. Meanwhile, Egger’s test of publication bias was not performed on this analysis due to the insufficient number of included studies. Finally, the participants were all from Asian countries with high incidence of gastric cancer (South Korea and Japan). The conclusions of this study cannot be directly applied to other countries. Thus, a prospective randomized trial that compare LPG-DT with LTG should be performed to confirm these observations.
This review showed that due to comparable clinical effect, LPG-DT is comparable to LTG for patients with proximal EGC. In addition, LPG-DT not only appears superior in preventing vitamin B12 deficiency, but also does not increase a risk of anastomotic stricture and reflux esophagitis compared to LTG.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional files.
American Society of Anesthesiologist
early gastric cancer
laparoscopic proximal gastrectomy
laparoscopic proximal gastrectomy with double-tract reconstruction
laparoscopic total gastrectomy
Newcastle-Ottawa Quality Assessment Scale
proximal gastrectomy with double-tract reconstruction
Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols
weighted mean difference
Ahn HS, Lee HJ, Yoo MW, Jeong SH, Park DJ, Kim HH, Kim WH, Lee KU, Yang HK. Changes in clinicopathological features and survival after gastrectomy for gastric cancer over a 20-year period. Br J Surg. 2011;98:255–60. https://0-doi-org.brum.beds.ac.uk/10.1002/bjs.7310.
Lee SS, Chung HY, Kwon OK, Yu W. Long-term quality of life after distal subtotal and Total gastrectomy: symptom- and behavior-oriented consequences. Ann Surg. 2016;263:738–44. https://0-doi-org.brum.beds.ac.uk/10.1097/sla.0000000000001481.
Japanese gastric cancer treatment guidelines 2014 (ver. 4). Gastric Cancer. 2017;20:1–19. https://0-doi-org.brum.beds.ac.uk/10.1007/s10120-016-0622-4.
Yoo CH, Sohn BH, Han WK, Pae WK. Long-term results of proximal and total gastrectomy for adenocarcinoma of the upper third of the stomach. Cancer Res Treat. 2004;36:50–5. https://0-doi-org.brum.beds.ac.uk/10.4143/crt.2004.36.1.50.
Hosoda K, Yamashita K, Katada N, Moriya H, Mieno H, Shibata T, Sakuramoto S, Kikuchi S, Watanabe M. Potential benefits of laparoscopy-assisted proximal gastrectomy with esophagogastrostomy for cT1 upper-third gastric cancer. Surg Endosc. 2016;30:3426–36. https://0-doi-org.brum.beds.ac.uk/10.1007/s00464-015-4625-8.
Aburatani T, Kojima K, Otsuki S, Murase H, Okuno K, Gokita K, Tomii C, Tanioka T, Inokuchi M. Double-tract reconstruction after laparoscopic proximal gastrectomy using detachable ENDO-PSD. Surg Endosc. 2017;31:4848–56. https://0-doi-org.brum.beds.ac.uk/10.1007/s00464-017-5539-4.
Nomura E, Kayano H, Lee SW, Kawai M, Machida T, Yamamoto S, Nabeshima K, Nakamura K, Mukai M, Uchiyama K. Functional evaluations comparing the double-tract method and the jejunal interposition method following laparoscopic proximal gastrectomy for gastric cancer: an investigation including laparoscopic total gastrectomy. Surg Today. 2019;49:38–48. https://0-doi-org.brum.beds.ac.uk/10.1007/s00595-018-1699-7.
Rosa F, Quero G, Fiorillo C, Bissolati M, Cipollari C, Rausei S, Chiari D, Ruspi L, de Manzoni G, Costamagna G, Doglietto GB, Alfieri S. Total vs proximal gastrectomy for adenocarcinoma of the upper third of the stomach: a propensity-score-matched analysis of a multicenter western experience (on behalf of the Italian research Group for Gastric Cancer-GIRCG). Gastric Cancer. 2018;21:845–52. https://0-doi-org.brum.beds.ac.uk/10.1007/s10120-018-0804-3.
Katai H, Mizusawa J, Katayama H, Kunisaki C, Sakuramoto S, Inaki N, Kinoshita T, Iwasaki Y, Misawa K, Takiguchi N, Kaji M, Okitsu H, Yoshikawa T, Terashima M. Single-arm confirmatory trial of laparoscopy-assisted total or proximal gastrectomy with nodal dissection for clinical stage I gastric cancer: Japan clinical oncology group study JCOG1401. Gastric Cancer. 2019;22:999–1008. https://0-doi-org.brum.beds.ac.uk/10.1007/s10120-019-00929-9.
Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pmed1000097.
Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25:603–5. https://0-doi-org.brum.beds.ac.uk/10.1007/s10654-010-9491-z.
Cho M, Son T, Kim HI, Noh SH, Choi S, Seo WJ, Roh CK, Hyung WJ. Similar hematologic and nutritional outcomes after proximal gastrectomy with double-tract reconstruction in comparison to total gastrectomy for early upper gastric cancer. 2019;33:1757–68. https://0-doi-org.brum.beds.ac.uk/10.1007/s00464-018-6448-x.
Furukawa H, Kurokawa Y, Takiguchi S, Tanaka K, Miyazaki Y, Makino T, Takahashi T, Yamasaki M, Nakajima K, Mori M, Doki Y. Short-term outcomes and nutritional status after laparoscopic subtotal gastrectomy with a very small remnant stomach for cStage I proximal gastric carcinoma. Gastric Cancer. 2018;21:500–7. https://0-doi-org.brum.beds.ac.uk/10.1007/s10120-017-0755-0.
Jung DH, Lee Y, Kim DW, Park YS, Ahn SH, Park DJ, Kim HH. Laparoscopic proximal gastrectomy with double tract reconstruction is superior to laparoscopic total gastrectomy for proximal early gastric cancer. Surg Endosc. 2017;31:3961–9. https://0-doi-org.brum.beds.ac.uk/10.1007/s00464-017-5429-9.
Kim DJ, Kim W. Laparoscopy-assisted proximal gastrectomy with double tract anastomosis is beneficial for vitamin B12 and Iron absorption. Anticancer Res. 2016;36:4753–8. https://0-doi-org.brum.beds.ac.uk/10.21873/anticanres.11031.
Park JY, Park KB, Kwon OK, Yu W. Comparison of laparoscopic proximal gastrectomy with double-tract reconstruction and laparoscopic total gastrectomy in terms of nutritional status or quality of life in early gastric cancer patients. Eur J Surg Oncol. 2018;44:1963–70. https://0-doi-org.brum.beds.ac.uk/10.1016/j.ejso.2018.08.014.
Sugiyama M, Oki E, Ando K, Nakashima Y, Saeki H, Maehara Y. Laparoscopic proximal gastrectomy maintains body weight and skeletal muscle better than Total gastrectomy. World J Surg. 2018;42:3270–6. https://0-doi-org.brum.beds.ac.uk/10.1007/s00268-018-4625-7.
Nakamura M, Nakamori M, Ojima T, Katsuda M, Iida T, Hayata K, Matsumura S, Kato T, Kitadani J, Iwahashi M, Yamaue H. Reconstruction after proximal gastrectomy for early gastric cancer in the upper third of the stomach: an analysis of our 13-year experience. Surgery. 2014;156:57–63. https://0-doi-org.brum.beds.ac.uk/10.1016/j.surg.2014.02.015.
Nozaki I, Hato S, Kobatake T, Ohta K, Kubo Y, Kurita A. Long-term outcome after proximal gastrectomy with jejunal interposition for gastric cancer compared with total gastrectomy. World J Surg. 2013;37:558–64. https://0-doi-org.brum.beds.ac.uk/10.1007/s00268-012-1894-4.
Hayami M, Hiki N, Nunobe S, Mine S, Ohashi M, Kumagai K, Ida S, Watanabe M, Sano T, Yamaguchi T. Clinical outcomes and evaluation of laparoscopic proximal gastrectomy with double-flap technique for early gastric Cancer in the upper third of the stomach. Ann Surg Oncol. 2017;24:1635–42. https://0-doi-org.brum.beds.ac.uk/10.1245/s10434-017-5782-x.
Ichikura T, Chochi K, Sugasawa H, Mochizuki H. Antireflux contrivance in jejunal pouch reconstruction after total and proximal gastrectomies. Dig Surg. 2006;23:381–6. https://0-doi-org.brum.beds.ac.uk/10.1159/000097898.
Masuzawa T, Takiguchi S, Hirao M, Imamura H, Kimura Y, Fujita J, Miyashiro I, Tamura S, Hiratsuka M, Kobayashi K, Fujiwara Y, Mori M, Doki Y. Comparison of perioperative and long-term outcomes of total and proximal gastrectomy for early gastric cancer: a multi-institutional retrospective study. World J Surg. 2014;38:1100–6. https://0-doi-org.brum.beds.ac.uk/10.1007/s00268-013-2370-5.
Nishigori T, Okabe H, Tsunoda S, Shinohara H, Obama K, Hosogi H, Hisamori S, Miyazaki K, Nakayama T, Sakai Y. Superiority of laparoscopic proximal gastrectomy with hand-sewn esophagogastrostomy over total gastrectomy in improving postoperative body weight loss and quality of life. Surg Endosc. 2017;31:3664–72. https://0-doi-org.brum.beds.ac.uk/10.1007/s00464-016-5403-y.
Yoon SS, Yang HK. Lymphadenectomy for gastric adenocarcinoma: should west meet east? Oncologist. 2009;14:871–82. https://0-doi-org.brum.beds.ac.uk/10.1634/theoncologist.2009-0070.
Strong VE, Song KY, Park CH, Jacks LM, Gonen M, Shah M, Coit DG, Brennan MF. Comparison of gastric cancer survival following R0 resection in the United States and Korea using an internationally validated nomogram. Ann Surg. 2010;251:640–6. https://0-doi-org.brum.beds.ac.uk/10.1097/SLA.0b013e3181d3d29b.
Gholami S, Janson L, Worhunsky DJ, Tran TB, Squires MH 3rd, Jin LX, Spolverato G, Votanopoulos KI, Schmidt C, Weber SM, Bloomston M, Cho CS, Levine EA, Fields RC, Pawlik TM, Maithel SK, Efron B, Norton JA, Poultsides GA. Number of lymph nodes removed and survival after gastric Cancer resection: An analysis from the US gastric Cancer collaborative. J Am Coll Surg. 2015;221:291–9. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jamcollsurg.2015.04.024.
Hsu JT, Lin CJ, Sung CM, Yeh HC, Chen TH, Chen TC, Chiang KC, Yeh TS, Hwang TL, Jan YY. Prognostic significance of the number of examined lymph nodes in node-negative gastric adenocarcinoma. Eur J Surg Oncol. 2013;39:1287–93. https://0-doi-org.brum.beds.ac.uk/10.1016/j.ejso.2013.07.183.
Okajima W, Komatsu S, Ichikawa D, Kosuga T, Kubota T, Okamoto K, Konishi H, Shiozaki A, Fujiwara H, Otsuji E. Prognostic impact of the number of retrieved lymph nodes in patients with gastric cancer. J Gastroenterol Hepatol. 2016;31:1566–71. https://0-doi-org.brum.beds.ac.uk/10.1111/jgh.13306.
Gu L, Chen M, Khadaroo PA, Ma X, Kong L, Li X, Zhu H, Zhong X, Pan J, Wang X. A risk-scoring model for predicting lymph node metastasis in early gastric Cancer patients: a retrospective study and external validation. J Gastrointest Surg. 2018;22:1508–15. https://0-doi-org.brum.beds.ac.uk/10.1007/s11605-018-3816-8.
An JY, Youn HG, Choi MG, Noh JH, Sohn TS, Kim S. The difficult choice between total and proximal gastrectomy in proximal early gastric cancer. Am J Surg. 2008;196:587–91. https://0-doi-org.brum.beds.ac.uk/10.1016/j.amjsurg.2007.09.040.
Hu Y, Kim HI, Hyung WJ, Song KJ, Lee JH, Kim YM, Noh SH. Vitamin B (12) deficiency after gastrectomy for gastric cancer: an analysis of clinical patterns and risk factors. Ann Surg. 2013;258:970–5. https://0-doi-org.brum.beds.ac.uk/10.1097/sla.0000000000000214.
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Li, S., Gu, L., Shen, Z. et al. A meta-analysis of comparison of proximal gastrectomy with double-tract reconstruction and total gastrectomy for proximal early gastric cancer. BMC Surg 19, 117 (2019). https://0-doi-org.brum.beds.ac.uk/10.1186/s12893-019-0584-7
- Proximal gastrectomy
- Total gastrectomy
- Early gastric cancer