|Year : 2021 | Volume
| Issue : 4 | Page : 423-434
Long-term and short-term outcomes after laparoscopic versus open surgery for advanced gastric cancer: An updated meta-analysis
Wei Zhang1, Zhangkan Huang2, Jianwei Zhang1, Xu Che3
1 Department of Pancreatic and Gastric Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Chaoyang District, Beijing, China
2 Department of Hepatobiliary and Pancreatic Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China
3 Department of Pancreatic and Gastric Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Chaoyang District, Beijing; Department of Hepatobiliary and Pancreatic Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China
|Date of Submission||12-Sep-2020|
|Date of Acceptance||19-Jan-2021|
|Date of Web Publication||06-May-2021|
Dr. Xu Che
Department of Pancreatic and Gastric Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 17 Panjiayuan Nanli, Chaoyang District, Beijing 100021; Department of Hepatobiliary and Pancreatic Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518116
Source of Support: None, Conflict of Interest: None
Background: The efficacy of laparoscopy for advanced gastric cancer (AGC) remains controversial.
Materials and Methods: We conducted a literature search on the EMBASE, PubMed and Cochrane Library databases to identify relevant available articles published between the time of the databases' inception and July 2020.
Results: A total of 14,689 patients were included in the 41 studies identified. A total of 6976 patients were in an laparoscopic approach group (LG) and 7713 patients were in an open approach group (OG). The meta-analysis showed that in randomized control trials (RCTs), LG were better than OG in terms of estimated blood loss, time to oral intake and time to first flatus while the operation time and proximal resection margin (PRM) were significantly worse in LG than in OG. In the non-RCTs, LG had shorter hospital stays, less blood loss, less intraoperative transfusion, less time to oral intake, time to first flatus, time to ambulation; less overall or serious complications; and better 3-year and 5-year overall or disease-free survival (DFS). Operation times and PRM were significantly worse for LGs.
Conclusion: The safety and effectiveness of laparoscopic surgery for AGC is not inferior to that of traditional open surgery, and to a certain extent, can reduce trauma, facilitate recovery, and be validated in RCTs and non-RCTs. In the real-world cohort, laparoscopic surgery for gastric cancer achieved a better survival rate and DFS rate. However, to evaluate the efficacy of these two methods more comprehensively, high-quality randomized controlled trials and longer follow-up times are still needed.
Keywords: Advanced gastric cancer, D2 lymph node dissection, gastrectomy, laparoscopy, meta-analysis, open
|How to cite this article:|
Zhang W, Huang Z, Zhang J, Che X. Long-term and short-term outcomes after laparoscopic versus open surgery for advanced gastric cancer: An updated meta-analysis. J Min Access Surg 2021;17:423-34
|How to cite this URL:|
Zhang W, Huang Z, Zhang J, Che X. Long-term and short-term outcomes after laparoscopic versus open surgery for advanced gastric cancer: An updated meta-analysis. J Min Access Surg [serial online] 2021 [cited 2021 Dec 5];17:423-34. Available from: https://www.journalofmas.com/text.asp?2021/17/4/423/315526
| ¤ Introduction|| |
Gastric cancer is a common malignant tumour of the digestive system that has a high incidence rate. Due to the lack of typical symptoms in the early stage, the diagnosis of gastric cancer often occurs in the advanced stage or even the late stage, typically with a poor prognosis. Advanced gastric cancer (AGC) is a subtype of gastric cancer. It mainly refers to the infiltration of cancer cells into the muscular layer and the serous layer of the gastric wall, but without distant metastasis occurring. At this stage, the risk of cancer cell metastasis is high, and can easily develop into a disseminated (or metastatic) cancer. Therefore, patients with AGC need to be actively treated. Radical gastrectomy and local lymph node dissection are the main methods used to treat gastric cancer. In 1994, Kitano et al. reported the first case of early gastric cancer (EGC) undergoing laparoscopic gastrectomy and a Billroth reconstruction. In the following 10 years, a large number of studies reported that laparoscopic radical surgery has obvious advantages of being minimally invasive, and achieved similar short-term and long-term results compared with traditional open radical surgery for EGC. Most of the current guidelines regard laparoscopic gastrectomy as the standard operation for EGC. In the past 10 years, since more and more minimally invasive surgeries for EGC have been performed, and the learning curve for laparoscopy is short, a large number of researchers have tried to use laparoscopy for the treatment of AGC. However, there is still no consensus on whether laparoscopic radical surgery can be performed for AGC. Controversies surrounding this idea focus on whether laparoscopic lymphadenectomy is safe and can meet the requirements of radical surgery. In this article, we systematically reviewed the literature on laparoscopic and open radical surgery in patients with AGC, and discussed the feasibility, safety and long effect of laparoscopic radical surgery for AGC through a cohort study in the real world, and with randomised control trials (RCTs) in the ideal environment.
| ¤ Materials and methods|| |
This meta-analysis was reported according to the preferred reporting items for systematic reviews and meta-analyses.
We conducted a literature search on the EMBASE, PubMed, and Cochrane Library databases to identify relevant available articles published between the time of the databases' inception and July 2020. Keywords searched for included laparoscopy, laparoscopy-assisted, open, laparotomy, AGC; the search strategy is ((Advanced gastric cancer) AND (Laparoscop*)) AND (open). We also reviewed the reference lists of the included studies for relevant studies we may have missed. We contacted the original authors to obtain extra information if necessary. If multiple studies were included from the same author or research centre, and the sample size was repeated, only the latest one with the largest sample size and the highest quality was selected. Studies with overlapping cases but no overlap in the reported outcome indicators were still included in the analysis as an independent study. The detailed steps of our literature search are shown in [Figure 1].
|Figure 1: Preferred reporting items for systematic reviews and meta-analyses 2009 flow diagram|
Click here to view
(1) Participants: AGC was diagnosed and a radical operation was performed; (2) The original data were published in the literature, in which there were independent reports on the relative efficacy of laparoscopic approach group (LG) compared to that of open approach group (OG) in the treatment of AGC, including a randomised-controlled, prospective or retrospective cohort study. (3) Study sample size: Unlimited; (4) follow-up time: Unlimited; (5) language of the published literature: Unlimited; research type: Human research.
Exclusion criteria and quality assessment
(1) Incomplete information, no extractable valid data, the author could not be reached, or the author was unresponsive; re-published or unpublished research. (2) Studies reported outcomes from LG or OG alone, without comparisons. (3) AGC treatment without surgery or non-radical surgery. (4) Robot researches, reviews, case reports and animal experiments.
Randomised controlled trials (RCTs), retrospective cohort studies and prospective cohort studies are included in this meta-analysis. The characteristics of these studies are presented in [Table 1]. In all the included studies, the RCTs conducted a risk assessment according to the 'risk assessment tool' recommended by the Cochrane Collaboration Network. The results from these assessments are attached in [Figure 2]. Quality evaluation of cohort studies are based on the Newcastle-Ottawa Scale (NOS).Details are shown in [Table 2].
|Figure 2: Review authors' judgements about all cohort studies according to the “risk assessment tool” recommended by the Cochrane Collaboration Network|
Click here to view
|Table 1: Basic characteristics and quality assessment of enrolled documents|
Click here to view
|Table 2: The risk of bias in the included retrospective cohort studies (by the Newcastle-Ottawa quality assessment tool)|
Click here to view
This meta-analysis used Review Manager 5.3 (The Cochrane Collaboration, Oxford, UK) for statistical analysis. The Haenszel method was used to estimate the effects from the merging binaries (relative risk, [RR]), and the inverse variance method was used to merge the effects from continuous data (weighted mean difference, [WMD]). RRs and WMDs with a 95% confidence interval (CI) were calculated to compare the incidence of postoperative indicators between the LG and OG groups. Heterogeneity among the included studies was qualitatively evaluated using a Chi-squared-based Q test. P < 0.10 showed statistically significant heterogeneity across the studies. The level of heterogeneity between studies was evaluated using I2 statistics. I2 < 30% was considered to have low heterogeneity, and a fixed-effects model was applied; 30%≤I2≤50% was considered to have moderate heterogeneity, and I2>50% represented high heterogeneity. When calculating the combined effect amount of a certain outcome index, only when the heterogeneity test in RCT and cohort study was I2 < 30% was the fixed effect model was used; otherwise, the random effect model was used to combine the amounts of the effects. Funnel charts were used for the qualitative evaluation of the publication bias. Stata software (version SE12.0) (Stata Corp., College Station, TX, USA) was used to calculate Begg's test and Egger's test for quantitative evaluation of publication bias of the included studies, with a significant level limited to 0.05.
| ¤ Results|| |
Search results and study selection
A total of 376 articles were retrieved by searching electronic databases and manually searching through relevant reference lists. We then excluded reviews, case reports, systematic reviews and meta-analyses, as well as studies that were clearly irrelevant based on their title or abstract. And after duplicates were identified and excluded, 51 articles remained. But because some studies come from the same authors or research centers, some of their results are from the same patients. If they are included again, the conclusions may be distorted. Therefore, we eliminated some studies with duplicate cases. Following these exclusions, only 42 articles (41 studies) remained. A total of 41 studies with a total of 14,689 patients were included in the final analysis. In total, 6976 patients (47.5%) received a laparoscopic approach, and 7713 (52.5%) patients received an open approach.
Results from the meta-analysis
We analysed 18 post-operative efficacy indexes of LGs and OGs in the treatment of AGC. The summary is shown in [Table 3]. The forest plots of recurrence rate, 3-year disease-free survival, 3-year disease-free survival, 5-year disease-free survival, and 5-year overall survival are respectively shown in [Figure 3][Figure 4][Figure 5][Figure 6][Figure 7].
|Table 3: Meta-analysis results of all outcome indicators in the available studies|
Click here to view
Sensitivity analysis and publication bias
A sensitivity analysis was conducted by excluding each study in each set's analysis. The sensitivity analysis of almost all outcome indicators showed that the combined effects between the RCT and cohort studies were stable, and a reversal of the cumulative analysis results did not been found. Funnel plots were used to evaluate publication biases [Figure 8]. The funnel diagram is a symmetrical distribution without an obvious extreme distribution value. No publication bias was detected by Begg's test and Egger's test in RCTs and RCSs. As shown in [Table 4].
|Figure 8: Funnel plot of (a) postoperative complications (b) recurrence (c) 5--year disease--free survival (d) 5--year overall survival|
Click here to view
| ¤ Discussion|| |
Laparoscopic treatment of EGC has been confirmed and recommended by the JGCA, CSCO and other clinical guidelines. However, its application in AGC remains controversial. AGC is usually accompanied by infiltration of the surrounding tissue and metastasis into surrounding lymph nodes. Surgical treatment requires not only resection of main cancer but also the implementation of an expanded radical operation in the surrounding tissue and lymph nodes, which is technically more difficult. In 1997, Goh et al. used laparoscopic surgery for the first time to treat four patients with AGC and achieved good results, initially demonstrating the feasibility of laparoscopic surgery for AGC. With the completion of several prospective, multicentre, high-quality, randomised controlled trials in Japan, Korea and China, the safety and effectiveness of laparoscopic surgery for AGC have been further verified. However, the application of laparoscopy in AGC in the real world is quite different in different countries and regions. A non-randomized study can reflect the effect of laparoscopy and laparotomy on locally AGC in a real environment. Therefore, this article systematically reviews the RCT and non-RCT literature, comparing the effects of laparoscopy on locally AGC with those of laparotomy, and systematically evaluates the advantages and disadvantages of laparoscopic treatments for late gastric cancer.
As the included research covers hospitals at all levels, in different regions, in different years; the quality of literature is uneven, and a specific literature quality assessment is shown in [Table 1]. For each observation outcome, a sensitivity analysis of the participating studies was conducted. The results of the meta-analysis showed that regardless whether the study was an RCT or a cohort study, the patients in the laparoscopic approach group had less estimated blood loss, less time to oral intake (d) (d) and less time to first flatus (d) after their operation. The operative time and PRM for the LGs were significantly worse than in the OGs. The distances of the distal margins, R0 rates, lymph node dissection and recurrence rates between the LG and OG were not statistically different. There was a higher frequency of hospital stays (d), intra-operative blood transfusions, overall/serious complications, 3-year OS, 3-year DFS, 5-year OS, 5-year DFS and in the LG compared to the OG in non-randomised controlled studies, and there were no significant differences in these frequencies in randomised controlled trials (RCTs). In the ideal RCT environment, there was no significant difference between the LG and the OG, but in the real world, the LGs had better outcomes than the OGs.
The number of lymph nodes removed was used to assess tumour adequacy. According to the International Union for Cancer Control, pathological examination of at least 15 lymph nodes is beneficial. In our review, most of the studies were conducted in Eastern countries, while most Asian surgeons preferred D2 dissections. The number of lymph nodes retrieved in the literature is sufficient. The meta-analysis showed that there was no significant difference in RCT between the two types of procedures. Some studies have shown that surgeons need to have 30–50 cases of laparoscopies with D1 removed to overcome the learning curve.,,, The anatomy of gastric tissues and organs is complex, the distribution of blood vessels is dense, and there will be variation in the process of operation. AGC requires D2 lymph node dissection, which is difficult and complex to operate on. Therefore, it is difficult for less experienced surgeons. AGC is not recommended in hospitals with fewer patients.
The scope of a laparoscopic radical resection follows the principle of open surgery. The operation scope of local AGC should include the resection of more than two-thirds of the stomach, as well as a D2 lymph node dissection. Most of the existing data are limited to the distal part of the stomach, most of which are performed with a distal resection, and few have undergone total gastrectomy. The distance between the cut edges for gastric cancer and tumours should be >3 cm for local gastric cancer and 5 cm for invasive gastric cancer. The meta-analysis showed that in both RCTs and RCSs, there was no significant difference in the distance between the distal margins and the tumour, while the distance between the proximal margin and the tumour for laparoscopies was significantly smaller than for open approaches. However, there was no significant difference in the rate of R0 between RCTs and retrospective studies. The recurrence rates for different literature follow-up times were different, as were the statistical recurrence time intervals. The recurrence rate of the combination had greater heterogeneity, but the meta-analysis results show that LG and the OG recurrence rates had no significant differences.
The meta-analysis of long-term oncology results showed that in the cohort study, OS and DFS at 3 and 5 years was better in the LG than in the OG. Most patients with AGC underwent adjuvant chemotherapy. However, in terms of evidence-based medicine, this study verified that laparoscopy has the advantages of small trauma and fast functional recovery (short hospitalisation time, less blood loss, less blood loss during the operation; shorter time for getting out of bed for the first time, for drinking water through the mouth for the first time, and shorter time for flatus and defecation to occur after the first operation). This advantage is likely to translate into better compliance with adjuvant chemotherapy in gastric cancer patients, where LGs can obtain earlier chemotherapy and complete more postoperative chemotherapy cycles. LGs are less likely to terminate chemotherapy due to adverse reactions, improving their post-operative survival rate., This phenomenon also occurs in colorectal cancer.
| ¤ Conclusion|| |
The safety and effectiveness of laparoscopic surgery for AGC are not inferior to that of traditional open surgery, and to a certain extent, reduces trauma, is conducive to recovery and has been verified on RCT. In the real-world cohort, laparoscopic radical gastrectomy can achieve a better survival rate and DFS rate. This may be related to the minimally invasive advantages brought by laparoscopy, which improve patient tolerance and completion of subsequent treatment. However, to evaluate the efficacy of these two methods more comprehensively, high quality, randomised controlled trials, and longer follow-up times are still needed.
This study has the following limitations. 1. Due to the inclusion of almost all studies on laparoscopic and open access methods for AGC, there is high heterogeneity in these articles, which limits the interpretation of individual research results. 2. Most of the included studies are retrospective studies, which cannot avoid selection biases.
Financial support and sponsorship
This research is supported by the Sanming Project of Medicine in Shenzhen (No.SZSM 201911008).
Conflicts of interest
Wei Zhang and Zhangkan Huang contributed equally to this work.
There is no conflict of interest among the authors.
| ¤ References|| |
Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines 2014 (ver. 4). Gastric Cancer 2017;20:1-9.
Kitano S, Iso Y, Moriyama M, Sugimachi K. Laparoscopy-assisted Billroth I gastrectomy. Surg Laparosc Endosc 2013;23:480.
Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JP, et al
. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: Explanation and elaboration. Ann Intern Med 2009;151:W65-94.
Cai J, Wei D, Gao CF, Zhang CS, Zhang H, Zhao T. A prospective randomized study comparing open versus laparoscopy-assisted D2 radical gastrectomy in advanced gastric cancer. Dig Surg 2011;28:331-7.
Chen QY, Huang CM, Lin JX, Zheng CH, Li P, Xie JW, et al
. Laparoscopy-assisted versus open D2 radical gastrectomy for advanced gastric cancer without serosal invasion: A case control study. World J Surg Oncol 2012;10:248.
Chen XZ, Wang SY, Wang YS, Jiang ZH, Zhang WH, Liu K, et al
. Comparisons of short-term and survival outcomes of laparoscopy-assisted versus open total gastrectomy for gastric cancer patients. Oncotarget 2017;8:52366-80.
DU XH, Li R, Chen L, Shen D, Li SY, Guo Q. Laparoscopy-assisted D2 radical distal gastrectomy for advanced gastric cancer: Initial experience. Chin Med J (Engl) 2009;122:1404-7.
Hamabe A, Omori T, Tanaka K, Nishida T. Comparison of long-term results between laparoscopy-assisted gastrectomy and open gastrectomy with D2 lymph node dissection for advanced gastric cancer. Surg Endosc 2012;26:1702-9.
Hu Y, Huang C, Sun Y, Su X, Cao H, Hu J, et al
. Morbidity and mortality of laparoscopic versus open D2 distal gastrectomy for advanced gastric cancer: A randomized controlled trial. J Clin Oncol 2016;34:1350-7.
Huang JL, Wei HB, Zheng ZH, Wei B, Chen TF, Huang Y, et al
. Laparoscopy-assisted D2 radical distal gastrectomy for advanced gastric cancer. Dig Surg 2010;27:291-6.
Huang X, Du H, Aihemaiti M, Liu T, Chen N, Yu W, et al
. Laparoscopic-assisted versus open D2 gastrectomy for advanced gastric cancer in highly selective patients: Short-term surgical and chemotherapy outcomes of a prospective cohort study. Am J Clin Oncol 2019;42:459-65.
Hwang SI, Kim HO, Yoo CH, Shin JH, Son BH. Laparoscopic-assisted distal gastrectomy versus open distal gastrectomy for advanced gastric cancer. Surg Endosc 2009;23:1252-8.
Kim KH, Kim MC, Jung GJ, Choi HJ, Jang JS, Kwon HC. Comparative analysis of five-year survival results of laparoscopy-assisted gastrectomy versus open gastrectomy for advanced gastric cancer: A case-control study using a propensity score method. Dig Surg 2012;29:165-71.
Kim SH, Chung Y, Kim YH, Choi SI. Oncologic outcomes after laparoscopic and open distal gastrectomy for advanced gastric cancer: Propensity score matching analysis. J Gastric Cancer 2019;19:83-91.
Kinoshita T, Uyama I, Terashima M, Noshiro H, Nagai E, Obama K, et al
. Long-term outcomes of laparoscopic versus open surgery for clinical stage II/III gastric cancer: A multicenter cohort study in Japan (LOC-A Study). Ann Surg 2019;269:887-94.
Lee HJ, Hyung WJ, Yang HK, Han SU, Park YK, An JY, et al
. Short-term outcomes of a multicenter randomized controlled trial comparing laparoscopic distal gastrectomy with D2 lymphadenectomy to open distal gastrectomy for locally advanced gastric cancer (KLASS-02-RCT). Ann Surg 2019;270:983-91.
Li Q, Wang J, Zhang G, Wang J, Yang B, Zhang Z. Feasibility and safety comparison of laparoscopy-assisted versus open gastrectomy for advanced gastric carcinoma with D2 lymphadenectomy. Jpn J Clin Oncol 2016;46:323-8.
Li Z, Shan F, Wang Y, Li S, Jia Y, Zhang L, et al
. Laparoscopic versus open distal gastrectomy for locally advanced gastric cancer after neoadjuvant chemotherapy: Safety and short-term oncologic results. Surg Endosc 2016;30:4265-71.
Li Z, Shan F, Ying X, Zhang Y, E JY, Wang Y, et al
. Assessment of laparoscopic distal gastrectomy after neoadjuvant chemotherapy for locally advanced gastric cancer: A randomized clinical trial. JAMA Surg 2019;154:1093-101.
Lin JX, Huang CM, Zheng CH, Li P, Xie JW, Wang JB, et al
. Laparoscopy-assisted gastrectomy with D2 lymph node dissection for advanced gastric cancer without serosa invasion: A matched cohort study from South China. World J Surg Oncol 2013;11:4.
Park YK, Yoon HM, Kim YW, Park JY, Ryu KW, Lee YJ, et al
. Laparoscopy-assisted versus Open D2 Distal Gastrectomy for Advanced Gastric Cancer: Results From a Randomized Phase II Multicenter Clinical Trial (COACT 1001). Ann Surg 2018;267:638-45.
Sato H, Shimada M, Kurita N, Iwata T, Nishioka M, Morimoto S, et al
. Comparison of long-term prognosis of laparoscopy-assisted gastrectomy and conventional open gastrectomy with special reference to D2 lymph node dissection. Surg Endosc 2012;26:2240-6.
Shi Y, Xu X, Zhao Y, Qian F, Tang B, Hao Y, et al
. Short-term surgical outcomes of a randomized controlled trial comparing laparoscopic versus open gastrectomy with D2 lymph node dissection for advanced gastric cancer. Surg Endosc 2018;32:2427-33.
Shinohara T, Satoh S, Kanaya S, Ishida Y, Taniguchi K, Isogaki J, et al
. Laparoscopic versus open D2 gastrectomy for advanced gastric cancer: A retrospective cohort study. Surg Endosc 2013;27:286-94.
Son T, Hyung WJ, Lee JH, Kim YM, Noh SH. Minimally invasive surgery for serosa-positive gastric cancer (pT4a) in patients with preoperative diagnosis of cancer without serosal invasion. Surg Endosc 2014;28:866-74.
Wang Z, Xing J, Cai J, Zhang Z, Li F, Zhang N, et al
. Short-term surgical outcomes of laparoscopy-assisted versus open D2 distal gastrectomy for locally advanced gastric cancer in North China: A multicenter randomized controlled trial. Surg Endosc 2019;33:33-45.
Wu LM, Jiang XJ, Lin QF, Jian CX. Comparative study of clinical efficacy of laparoscopy-assisted radical gastrectomy versus open radical gastrectomy for advanced gastric cancer. Genet Mol Res 2015;14:3459-65.
Zhao XF, Jeong O, Jung MR, Ryu SY, Park YK. A propensity score-matched case-control comparative study of laparoscopic and open extended (D2) lymph node dissection for distal gastric carcinoma. Surg Endosc 2013;27:2792-800.
Zhao Y, Yu P, Hao Y, Qian F, Tang B, Shi Y, et al
. Comparison of outcomes for laparoscopically assisted and open radical distal gastrectomy with lymphadenectomy for advanced gastric cancer. Surg Endosc 2011;25:2960-6.
Shibuya K, Kawamura H, Takahashi S, Ohno Y, Ichikawa N, Yoshida T, et al
. Short-term and Long-term Outcomes Following Laparoscopic Gastrectomy for Advanced Gastric Cancer Compared With Open Gastrectomy. Surg Laparosc Endosc Percutan Tech 2019;29:297-303.
Wang JB, Zhong Q, Chen QY, Lin GT, Liu ZY, Huang XB, et al
. Well-designed retrospective study versus small-sample prospective study in research based on laparoscopic and open radical distal gastrectomy for advanced gastric cancer. Surg Endosc 2020;34:4504-15.
Xu Y, Hua J, Li J, Shi L, Xue H, Shuang J, et al
. Long-term outcomes of laparoscopic versus open gastrectomy for advanced gastric cancer: A large cohort study. Am J Surg 2019;217:750-6.
Wang N, Zhou A, Jin J, Huang H, Zhang Y, Chen Y, et al
. Open vs. laparoscopic surgery for locally advanced gastric cancer after neoadjuvant therapy: Short-term and long-term survival outcomes. Oncol Lett 2020;20:861-7.
Wang H, Mou T, Chen H, Hu Y, Lin T, Li T, et al
. Long-term outcomes of laparoscopy-assisted distal gastrectomy versus open distal gastrectomy for gastric cancer: A 10-year single-institution experience. Surg Endosc 2019;33:135-44.
Inokuchi M, Nakagawa M, Tanioka T, Okuno K, Gokita K, Kojima K. Long- and short-term outcomes of laparoscopic gastrectomy versus open gastrectomy in patients with clinically and pathological locally advanced gastric cancer: A propensity-score matching analysis. Surg Endosc 2018;32:735-42.
Ludwig K, Schneider-Koriath S, Scharlau U, Steffen H, Möller D, Bernhardt J. Totally laparoscopic versus open gastrectomy for gastric cancer: A matched pair analysis. Zentralbl Chir 2018;143:145-54.
Zhang X, Sun F, Li S, Gao W, Wang Y, Hu SY. A propensity score-matched case-control comparative study of laparoscopic and open gastrectomy for locally advanced gastric carcinoma. J BUON 2016;21:118-24.
Zhang Y, Qi F, Jiang Y, Zhai H, Ji Y. Long-term follow-up after laparoscopic versus open distal gastrectomy for advanced gastric cancer. Int J Clin Exp Med 2015;8:13564-70.
Chan BYO, Yau KKW, Chan CKO. Totally laparoscopic versus open gastrectomy for advanced gastric cancer: A matched retrospective cohort study. Hong Kong Med J 2019;25:30-7.
Shi Y, Xu X, Zhao Y, Qian F, Tang B, Hao Y, et al
. Long-term oncologic outcomes of a randomized controlled trial comparing laparoscopic versus open gastrectomy with D2 lymph node dissection for advanced gastric cancer. Surgery 2019;165:1211-6.
Sica GS, Iaculli E, Biancone L, Di Carlo S, Scaramuzzo R, Fiorani C, et al
. Comparative study of laparoscopic vs open gastrectomy in gastric cancer management. World J Gastroenterol 2011;17:4602-6.
Yu J, Huang C, Sun Y, Su X, Cao H, Hu J, et al
. Effect of Laparoscopic vs Open Distal Gastrectomy on 3-Year Disease-Free Survival in Patients With Locally Advanced Gastric Cancer: The CLASS-01 Randomized Clinical Trial. JAMA 2019;321:1983-92.
Hur H, Jeon HM, Kim W. Laparoscopy-assisted distal gastrectomy with D2 lymphadenectomy for T2b advanced gastric cancers: Three years' experience. J Surg Oncol 2008;98:515-9.
Li Z, Li B, Bai B, Yu P, Lian B, Zhao Q. Long-term outcomes of laparoscopic versus open D2 gastrectomy for advanced gastric cancer. Surg Oncol 2018;27:441-8.
Lin JX, Huang CM, Zheng CH, Li P, Xie JW, Wang JB, et al
. Is all advanced gastric cancer suitable for laparoscopy-assisted gastrectomy with extended lymphadenectomy? A case-control study using a propensity score method. Ann Surg Oncol 2016;23:1252-60.
Goh PM, Khan AZ, So JB, Lomanto D, Cheah WK, Muthiah R, et al
. Early experience with laparoscopic radical gastrectomy for advanced gastric cancer. Surg Laparosc Endosc Percutan Tech 2001;11:83-7.
Yoo CH, Kim HO, Hwang SI, Son BH, Shin JH, Kim H. Short-term outcomes of laparoscopic-assisted distal gastrectomy for gastric cancer during a surgeon's learning curve period. Surg Endosc 2009;23:2250-7.
Jin SH, Kim DY, Kim H, Jeong IH, Kim MW, Cho YK, et al
. Multidimensional learning curve in laparoscopy-assisted gastrectomy for early gastric cancer. Surg Endosc 2007;21:28-33.
Kim MC, Jung GJ, Kim HH. Learning curve of laparoscopy-assisted distal gastrectomy with systemic lymphadenectomy for early gastric cancer. World J Gastroenterol 2005;11:7508-11.
Kunisaki C, Makino H, Yamamoto N, Sato T, Oshima T, Nagano Y, et al
. Learning curve for laparoscopy-assisted distal gastrectomy with regional lymph node dissection for early gastric cancer. Surg Laparosc Endosc Percutan Tech 2008;18:236-41.
Bao H, Xu N, Li Z, Ren H, Xia H, Li N, et al
. Effect of laparoscopic gastrectomy on compliance with adjuvant chemotherapy in patients with gastric cancer. Medicine (Baltimore) 2017;96:e6839.
Kim RH, Kavanaugh MM, Caldito GC. Laparoscopic colectomy for cancer: Improved compliance with guidelines for chemotherapy and survival. Surgery 2017;161:1633-41.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8]
[Table 1], [Table 2], [Table 3], [Table 4]
|This article has been cited by|
||Comparison of short-term results of open and laparoscopic surgery in gastric cancer at a new regional hospital: a single surgeon experience
| ||Beslen GOKSOY, Mevlut KIYAK, Gökhan YILMAZ, Ibrahim AZAMAT, Didem ERTORUL, Ömer INANÇ, Çigdem ARICAN, Ibrahim CIL, Mehmet BITIRIM |
| ||Journal of Health Sciences and Medicine. 2021; 4(5): 569 |
|[Pubmed] | [DOI]|