Journal of Minimally Invasive Surgery 2018; 21(4): 141-147
Function-Preserving Surgery in Gastric Cancer
Jan Andrew D. Bueno1,2, Young-Suk Park1, Sang-Hoon Ahn1, Do Joong Park1, and Hyung-Ho Kim1
1Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea, 2Department of Surgery, University of Santo Tomas Hospital, Philippines
Correspondence to: Do Joong Park, Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, 166 Gumi-ro, Bundang-gu, Seongnam 13620, Korea, Tel: +82-31-787-7097, Fax: +82-31-787-4078, E-mail:, ORCID:
Received: July 6, 2018; Revised: September 11, 2018; Accepted: September 12, 2018; Published online: December 15, 2018.
© Journal of Minimally Invasive Surgery. All rights reserved.

cc This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

The rising incidence of early gastric cancer has enabled the development of function-preserving gastrectomy with the focus on post gastrectomy quality of life and adherence to sound oncologic principles. It is concurrent with the growing popularity of minimally invasive surgery; and both are commonly used together. The different kinds of function-preserving gastrectomy included in this review are: pylorus-preserving and proximal gastrectomy, vagus nerve preservation, sentinel node navigation, and various endoscopic & minimally-invasive techniques. In this article the indications, techniques, oncologic safety, functional benefit, and outcomes of each kind of function-preserving gastrectomy are discussed.

Keywords: Function-preserving gastrectomy (FPG), Early gastric cancer (EGC), Pylorus-preserving gastrectomy (PPG), Proximal gastrectomy (PG), Laparoscopic gastrectomy

The proportion of early gastric cancer (EGC) in East Asia has been increasing due to the implementation of screening programs in South Korea and Japan. In 2014, Stage I gastric cancers comprised 63.9% of all patients who received surgical treatment for gastric cancer in South Korea.1 This made the prognosis for majority of gastric cancer patients favorable and thus the shift of focus on quality of life post gastrectomy is inevitable.

Function-preserving gastrectomy (FPG) was developed to prevent post-gastrectomy syndromes experienced after conventional radical gastrectomy. It is characterized by a less radical but curative resection that maintains the reservoir and mixing/grinding functions of the stomach, as well as its endocrine and metabolic function. It is concurrent with the popularity of laparoscopic surgery and thus are used in combination in some centers.

In this review article, the various types of FPG will be discussed which are: pylorus-preserving gastrectomy, proximal gastrectomy, vagus nerve-preserving gastrectomy, sentinel node navigation surgery, and endoscopic resection (EMR, ESD, LECS, CLEAN-NET, NEWS).


PPG was initially developed by Maki et al. for the treatment of benign ulcers in the middle third of the stomach and has then been adapted for treatment in EGC. Essential features of the procedure include: preservation of the sphincteric function of the pylorus and retaining of the storage function of the prepyloric antrum. With this technique, the physiological gastric emptying is theoretically maintained; hence, alkaline reflux, dumping syndrome, disturbed bowel habits, and weight loss may be reduced in contrast to the standard distal gastrectomy (DG) with Billroth I reconstruction.2

According to the Japanese gastric cancer treatment guidelines, 3 PPG can be considered for the treatment of clinical T1 N0 M0 gastric cancers in the middle portion of the stomach with distal tumor border at least 4 cm proximal to the pylorus.

The standard technique of pylorus preservation is comprised of preservation of the hepatic branch of the vagus nerve and the infra-pyloric vessels, with some minor variation among surgeons.4 This maintains the innervation, blood supply, and venous drainage of the pylorus.

D1/D1+ lymphadenectomy is recommended for cT1N0 gastric cancer patients according to the Japanese Gastric Cancer Guidelines, which for PPG, comprises dissection of lymph nodes station 1, 3, 4sb, 4sd, 6, & 7 for D1 and inclusion of 8a & 9 for D1+.3 Suprapyloric lymph node dissection is omitted to preserve the right gastric vessels and hepatic branch of the vagus, which has been considered a pitfall of PPG.5 However, a Japanese study reported a 0.2% rate of metastases to the suprapyloric lymph nodes in T1 cancers in the middle one–third of the stomach.6 CT scan and endoscopic ultrasound are commonly used pre-operatively to ascertain accuracy of the diagnosis of cT1N0 cases who are candidates for PPG.


In a study using quality-of-life questionnaires PPG was found-out to have significantly lower scores in diarrhea and dumping syndrome compared to DG.7 A meta-analysis8 involving 1,213 patients found PPG to be a preventive factor of dumping syndrome, bile reflux, gastritits, and gallstone formation, while proving to be beneficial in weight regain.

Delayed gastric emptying is one of the most common complications after PPG. Incidence of gastric stasis was 6.2%~7.8% in patients who underwent laparoscopy-assisted PPG.5 Postoperative edema and neurologic dysfunction have been theorized to cause such complication, therefore preservation of the vagal innervation and right gastric & infrapyloric veins for blood flow drainage are advocated in PPG.9 Nakane et al.10 reported a 35% incidence in delayed gastric emptying in patients with a 1.5 cm antral cuff length vs. 10% in patients with a 2.5 cm antral cuff length. The optimum antral cuff length is not yet established, but has tended to become longer in more recent studies.5

The 5-year survival rate of patients who underwent PPG was 98% in a study by Hiki et al.11 Comparing laparoscopy–assisted PPG to laparoscopy-assisted DG, Suh et al.12 reported a similar 3-year recurrence-free survival rate of 98.2% vs 98.8%, respectively. A meta-analysis by Xiao et al.8 showed a similar 5-year survival rate of PPG vs DG.

Laparoscopy in PPG

The use of laparoscopy in function-preserving gastrectomy has gained interest and popularity in the recent years. Laparoscopy-assisted PPG has been established as a feasible and safe procedure with reduced blood loss, pain, and faster recovery compared with open PPG.13 Anastomosis can be easily performed from a small upper abdominal incision directly above the anastomosis site (Fig. 1).

A multicenter randomized controlled trial comparing laparoscopic PPG vs laparoscopic DG (KLASS 04-Korean laparoscopic Gastrointestinal Surgery Study) is on-going in South Korea. It will primarily investigate the incidence of dumping syndrome, as well as the relapse-free & overall survival, morbidity, mortality, QOL, and other secondary outcome measures.

Totally laparoscopic PPG has also been reported, although a longer operative time is required compared to laparoscopy-assisted PPG.14 Anastomosis is done using intracorporeal delta-shaped anastomosis and a combination of stapler & handsewn procedures.2 Confirming the tumor location by use of pre-operative placement of marking clips and intraoperative gastroscopy has ensured the oncologic safety of this procedure.

Robotic gastrectomy has not been proven to be superior than laparoscopic gastrectomy.15 Although it may provide a superior operating environment, as it eliminates surgeon tremor and provides a highly magnified imaging with a steady fixed camera.5 Robot assisted PPG has been reported but has not shown any difference in terms of patient outcomes when compared to laparoscopy assisted PPG.16


The incidence of cancer in the upper third of the stomach is steadily rising. In 2014, there were 2,365 (16%) cases of cancers in the upper third of the stomach treated with surgery in South Korea, a 2.6% increase from 2009.1 In congruence with the growth of the proportion of EGC, laparoscopic PG is the best theoretical treatment option for proximal EGC and outweighs open PG, open total gastrectomy (TG), and laparoscopic TG.17 Quality of life may be improved with PG due to the preservation of the function of the distal stomach along with the pyloric ring.9 However, PG is not a popular surgical choice, with only 1.1% (168) of all gastrectomy cases done in South Korea at 2014.1 This is probably due to three main concerns with PG: functional benefits, oncological safety, and anastomosis-related complications. These will be discussed in the succeeding text.

The Japanese gastric cancer treatment guidelines 2014 (ver 4) recommends that PG can be considered for cT1N0 proximal gastric tumors where more than half of the distal stomach can be preserved; and D1/D1+ lymphadenectomy for cT1N0 tumors comprising lymph nodes 1, 2, 3a, 4sa, 4sb, & 7 for D1; with the inclusion of 8a, 9, & 11p for D1+.3 The distal stomach is preserved along with its blood supply (right gastric and right gastroepiploic vessels) and innervation (distal branches of the vagus nerve).


Many studies report conflicting benefit of PG compared to TG in terms of nutrition status (serum protein, albumin, and cholesterol), body weight, and anemia.1821 However, long-term follow-up data have shown that hemoglobin levels in PG are significantly higher than in TG, which is reflected in the lower requirement for vitamin B12 supplementation after PG compared to TG.22 Takiguchi et al.23 reported improved quality of life in terms of weight loss, necessity of additional meals, diarrhea, and dumping in patients who underwent open PG vs open TG.

The oncologic safety of PG is questioned due to the omission of dissection of lymph node stations 5 and 6 plus the potential of remnant stomach cancer. However, lymph node metastasis in EGC are estimated to be at 10~20%. Additionally, Kong et al.24 reported that proximal EGC only metastasize to LN stations 2, 3, and 7. And Kitamura et al.25 did not observe LN metastasis on the lower stomach among proximal gastric cancers confined to the muscularis propia (T2).

In a meta-analysis comprising 1,364 patients, the 5-year survival rate in PG was not statistically different with TG (60.9% vs 64.4%). But recurrence is expectedly higher in PG compared to TG (38.7% vs 24.4%).26

Remnant gastric cancer is higher after open PG (3.6~9.1%) than after open DG (0.4~2.5%).2 Endoscopic surveillance after surgery is an important tool for detection of recurrence. Although intubation of the endoscope can be difficult in PG with an esophagojejunostomy (EJ) reconstruction, especially with a greater than 10 cm interposed jejunal length.27

Esophagogastrostomy (EG) and EJ are the most frequently used reconstruction technique for PG. EG only involves one anastomosis, lesser operative time, and blood loss but has a higher frequency of postoperative reflux esophagitis and anastomotic stricture. Various modifications have been tried (gastropexy, fundoplication, gastric tube, lower esophageal sphincter preserving, etc.) but the anastomosis-related late complications were significantly higher in EG after PG compared to Roux-en-Y EJ after TG in various studies (27.4~67.4% vs 7.4~8.7%).18,19,26,28

EJ has been used to prevent the anastomosis-related complications of EG. Jejunal interposition, jejunal pouch, and double tract reconstruction (DTR) are among the EJ procedures done. EJ after PG is similar to Roux-en-Y EJ after TG in terms of anastomosis-related late complications (0~10.2% vs 1.8~8.7%).18,2931 Although abdominal fullness, discomfort rumbling, and hiccups are more frequently found after EJ in PG due to the disturbance of food passage by the interposed bowel.9

Laparoscopy in PG

Few studies have compared laparoscopic PG to open PG. Kinoshita et al.32 reported that laparoscopic PG has a longer operative time but decreased blood loss, and similar complication rates compared to open PG. The most important technical challenge in laparoscopic PG is the reconstruction method, which is still not well established.33 Ahn et al.33 reported a case series on laparoscopic PG using DTR and showed that it is a feasible, simple, and useful reconstruction method with excellent postoperative outcomes in terms of reflux symptoms (Fig. 2).

An on-going multicenter, prospective Phase III trial (KLASS 05) in South Korea aims to compare laparoscopic PG with DTR and laparoscopic TG, with hemoglobin change at 2 years post-gastrectomy and vitamin B12 cumulative supplement quantity as the primary endpoint.

Single-port laparoscopic PG with DTR has been reported by Lee et al.34 Despite the technical challenge caused by poor ergonomics, it provided cosmetic benefit and a good quality of life for the patient. The use of Robotics in a few cases of PG has been reported as part of general use of robotics in gastrectomy.15 There are no specific reports on the benefit of robotics in PG.


In conventional D2 gastrectomy for gastric cancer, the celiac and hepatic branches of the vagus are removed en bloc with the left gastric artery and the whole of the lesser omentum.35 Vagus nerve preservation in open gastrectomy was introduced in 1991 at Japan, for early gastric cancer cases to decrease postgastrectomy syndrome. In this procedure, the hepatic branches of the anterior vagal trunk that innervates the liver and biliary tract are preserved, as well as the celiac branches of the posterior vagal trunk which innervates the small intestines.36 It is an integral part of PPG and has been described in numerous articles. But is also used in early gastric cancers with distal, total, and proximal gastrectomy.35

For preservation of the hepatic branch, the lesser omentum should be divided below the nerve. During dissection of the common hepatic artery lymph nodes, the hepatic nerve plexus should be identified and preserved.36 The posterior trunk of the vagus nerve and its branches lie within the gastropancreatic peritoneal fold. Ando et al.35 identified three types of variations in the course of the celiac branch depending on its relationship to the left gastric artery, and found that 81.8% had the celiac branch lay closer to the artery than to the crus. Preservation of the celiac branch entails meticulous dissection when isolating the left gastric artery (Fig. 3).


The benefits of VNPG are seen in the superior recovery of body weight and reduction in the incidence of gallstone development.35 A randomized controlled trial37 in South Korea comparing vagus nerve-preserving distal gastrectomy to conventional gastrectomy showed significantly less diarrhea and appetite loss at 12 months with vagus nerve preservation. There was no difference in the long-term clinical complications, recurrence, and survival.

Laparoscopy in VNPG

Laparoscopic VNPG has been reported mostly in articles on laparoscopic PPG. Under the laparoscopic view, fine vessels and nerves are seen more clearly because of the magnification and thus might be more reliable than open techniques.36


The sentinel node (SN) is defined as the first lymph node to receive lymphatic drainage from the primary tumor, and lymph node metastasis is assumed to initially occur at this site.38 The principle of SNNS is to identify and check the SNs for metastasis so that excessive lymphadenectomy for non-pathologic nodes may be prevented and extent of gastric resection be minimized. This concept has been applied to breast cancer and melanoma treatment and has led to less morbidity and improved quality of life in patients.3941

But due to the multidirectional lymphatic drainage of the stomach and the possibility of skip metastasis, the application of SNNS in gastric cancer has been a challenge.38 Other issues with SNNS is the use of the appropriate tracer, how to identify & examine the SNs, options for primary tumor control, and which subgroup of patients will SNNS be applicable for.42

A combination of dye-based and radioisotope-based techniques are the most commonly used method for sentinel node mapping and identification. Peritumoral submucosal endoscopic injection of the dye is usually done and infrared fluorescence imaging of the surgical field has been used for better visualization. Hematoxylin and eosin has been the most commonly used technique for intraoperative diagnosis of metastasis in sentinel nodes and accuracy ranges from 74~100% in the literature.42 Other techniques include immunohistological staining and reverse transcriptase polymerase chain reaction, which seem promising especially with concerns on micrometastasis.42 For primary tumor control; the other function preserving gastrectomy methods such as PG & PPG have been used, as well as less extensive resections such as wedge resection, segmental resection, and various endoscopic full-thickness & local resection techniques,43 however there is no consensus on the optimal method.44 The studies from East Asia have used SNNS mostly in T1 and some in T2 tumors. Some Western studies included up to T3 tumors.42

The Japanese Society of Sentinel Node Navigation Surgery45 analyzed 397 patients with cT1-2N0M0 gastric cancers with <4 cm tumor size. They perfomed SN mapping and identification followed by standard gastrectomy with D2 lymphadenectomy. The detection rate, sensitivity, and accuracy of SN examination were 97.5% (387/397), 93% (53/57), and 99% (383/387), respectively. False-negative rate was only 1% (four patients). Their work also suggested that lymphatic basin based surgery (sentinel lymph node and downstream lymphatic flow) may be recommended due to findings of metastatic nodes in only the lymphatic basin of some cases with negative SNs.

The SENORITA trial (SEntinel Node ORIented Tailored Approach) in South Korea will evaluate stomach preserving surgery with sentinel basin dissection versus standard gastrectomy in terms of disease-free survival, morbidity, mortality, and quality of life in patients with early gastric cancer.38,44


Endoscopic resection is considered for tumors that have a very low possibility of lymph node metastasis and are suitable for en-bloc resection. Some are used as primary tumor control for SNNS. The two most frequently used methods of endoscopic resection are Endoscopic mucosal resection (EMR) and Endoscopic submucosal dissection (ESD). The Japanese gastric cancer treatment guidelines3 state that EMR or ESD is indicated as a standard treatment for gastric adenocarcinoma of the differentiated-type without ulcerative findings, of which the depth of invasion is clinically diagnosed as T1a and the diameter is ≤2 cm. Expanded indications have also been described but are considered investigational.

In EMR, the lesion, together with the surrounding mucosa, is lifted by submucosal injection of saline and removed using a high-frequency steel snare.3 A major limitation of EMR is incomplete resection of lesions >2 cm due to size limitation of the instruments used.46

While in ESD, the mucosa surrounding the lesion is circumferentially incised using a high-frequency electric knife and the submucosal layer is dissected from the proper muscle layer.3 The size limitation in EMR is addressed by ESD and is considered superior to EMR because it enables precise pathologic T staging for large EGC.46 In a recent metaanalysis,47 ESD was shown to have advantages in en bloc resection, histologically complete resection, and local recurrence rate compared to EMR. Although mean operation time and complications such as perforation was higher in the ESD technique.

Hahn et al.48 found that ESD had lower acute complication rates compared to surgery (8.1% vs 18.1%) but had similar 5 year-overall survival (96.4% vs 97.2%) and disease-specific survival rate (99.6% vs 99.2%). However, the annual incidence of recurrence was 2.18% in ESD and 0.19% in the surgery group.

Hybrid surgery or the concept of laparoscopic and endoscopic cooperative surgery (LECS) for early gastric cancer has been reported. Endoscopic full-thickness resection (EFTR) is usually done with laparoscopic assistance to facilitate safe resection of the lesion, repair of the ensuing defect, and even limited lymph node dissection.49 Dissection is done intraluminally with submucosal injection and circumferential endoscopic mucosal incision, followed by intentional perforation to facilitate complete full thickness resection under laparoscopic countertraction.50 Iatrogenic tumor seeding is a concern with this procedure since there is a possibility of tumor cells in the gastric juice to spread by spillage or by contact of exposed surface of the lesion with the peritoneum or laparoscopic instruments.49

Non-exposure techniques for full-thickness resection have been developed to prevent iatrogenic seeding such as wedge resection, combination of laparoscopic and endoscopic approaches to neoplasia with non-exposure technique (CLEAN-NET), and non-exposed endoscopic wall-inversion surgery (NEWS).49


Function-preserving gastrectomy has revolutionized treatment for early gastric cancer. The more popular types and techniques have been discussed in this review article and quite a few more are currently being developed with the advancement of skills & technology. There are important matters that have to be addressed in function-preserving gastrectomy, which are: oncologic safety, actual functional benefit for patients, proper selection of patients, availability and expertise in the use of new technique and equipment including laparoscopy and robotics.

Fig. 1. Gastro-gastric anastomosis after laparoscopic pylorus-preserving gastrectomy.
Fig. 2. Laparoscopic proximal gastrectomy with double tract reconstruction which comprises esophago-jejunostomy, gastro-jejunostomy and jejunojejunostomy.
Fig. 3. Vagus nerve-preserving gastrectomy. Hepatic and celiac branches are identified and preserved during the surgery.
  1. Information Committee of Korean Gastric Cancer Association (2016). Korean Gastric Cancer Association Nationwide Survey on Gastric Cancer in 2014. J Gastric Cancer. 16, 131-140.
    Pubmed KoreaMed CrossRef
  2. Nunobe, S, and Hiki, N (2017). Function-preserving surgery for gastric cancer: current status and future perspectives. Transl Gastroenterol Hepatol. 2, 77.
    Pubmed KoreaMed CrossRef
  3. Japanese Gastric Cancer Association (2017). Japanese gastric cancer treatment guidelines 2014 (ver. 4). Gastric Cancer. 20, 1-19.
    Pubmed KoreaMed CrossRef
  4. Shibata, C, Saijo, F, and Kakyo, M (2012). Current status of pylorus-preserving gastrectomy for the treatment of gastric cancer: a questionnaire survey and review of literatures. World J Surg. 36, 858-863.
    Pubmed CrossRef
  5. Oh, SY, Lee, HJ, and Yang, HK (2016). Pylorus-Preserving Gastrectomy for Gastric Cancer. J Gastric Cancer. 16, 63-71.
    Pubmed KoreaMed CrossRef
  6. Nakajima, T, and Yamaguchi, T (2006). Gastric Cancer Data Base in Cancer Institute, Japan; 1946–2004. Tokyo: Kanehara & Co, Ltd
  7. Fujita, J, Takahashi, M, and Urushihara, T (2016). Assessment of postoperative quality of life following pylorus-preserving gastrectomy and Billroth-I distal gastrectomy in gastric cancer patients: results of the nationwide postgastrectomy syndrome assessment study. Gastric Cancer. 19, 302-311.
    Pubmed CrossRef
  8. Xiao, XM, Gaol, C, Yin, W, Yu, WH, Qi, F, and Liu, T (2014). Pylorus-Preserving versus Distal Subtotal Gastrectomy for Surgical Treatment of Early Gastric Cancer: A Meta-Analysis. Hepatogastroenterology. 61, 870-879.
  9. Hiki, N, Nunobe, S, Kubota, T, and Jiang, X (2013). Function-preserving gastrectomy for early gastric cancer. Ann Surg Oncol. 20, 2683-2692.
    Pubmed CrossRef
  10. Nakane, Y, Michiura, T, Inoue, K, Sato, M, Nakai, K, and Yamamichi, K (2002). Length of the antral segment in pylorus-preserving gastrectomy. Br J Surg. 89, 220-224.
    Pubmed CrossRef
  11. Hiki, N, Sano, T, Fukunaga, T, Ohyama, S, Tokunaga, M, and Yamaguchi, T (2009). Survival benefit of pylorus-preserving gastrectomy in early gastric cancer. J Am Coll Surg. 209, 297-301.
    Pubmed CrossRef
  12. Suh, YS, Han, DS, and Kong, SH (2014). Laparoscopy-assisted pylorus-preserving gastrectomy is better than laparoscopy-assisted distal gastrectomy for middle-third early gastric cancer. Ann Surg. 259, 485-493.
  13. Nunobe, S, Hiki, N, and Fukunaga, T (2007). Laparoscopy-assisted pylorus-preserving gastrectomy: preservation of vagus nerve and infrapyloric blood flow induces less stasis. World J Surg. 31, 2335-2340.
    Pubmed CrossRef
  14. Kumagai, K, Hiki, N, and Nunobe, S (2015). Totally laparoscopic pylorus-preserving gastrectomy for early gastric cancer in the middle stomach: technical report and surgical outcomes. Gastric Cancer. 18, 183-187.
    Pubmed CrossRef
  15. Kim, HI, Han, SU, and Yang, HK (2016). Multicenter Prospective Comparative Study of Robotic Versus Laparoscopic Gastrectomy for Gastric Adenocarcinoma. Ann Surg. 263, 103-109.
    Pubmed CrossRef
  16. Han, DS, Suh, YS, and Ahn, HS (2015). Comparison of Surgical Outcomes of Robot-Assisted and Laparoscopy-Assisted Pylorus-Preserving Gastrectomy for Gastric Cancer: A Propensity Score Matching Analysis. Ann Surg Oncol. 22, 2323-2328.
    Pubmed CrossRef
  17. Jung, DH, Ahn, SH, Park, DJ, and Kim, HH (2015). Proximal Gastrectomy for Gastric Cancer. J Gastric Cancer. 15, 77-86.
    Pubmed KoreaMed CrossRef
  18. An, JY, Youn, HG, Choi, MG, Noh, JH, Sohn, TS, and Kim, S (2008). The difficult choice between total and proximal gastrectomy in proximal early gastric cancer. Am J Surg. 196, 587-591.
    Pubmed CrossRef
  19. Wen, L, Chen, XZ, and Wu, B (2012). Total vs. proximal gastrectomy for proximal gastric cancer: a systematic review and meta-analysis. Hepatogastroenterology. 59, 633-640.
    Pubmed CrossRef
  20. Kosuga, T, Ichikawa, D, and Komatsu, S (2015). Feasibility and Nutritional Benefits of Laparoscopic Proximal Gastrectomy for Early Gastric Cancer in the Upper Stomach. Ann Surg Oncol. 22, S929-935.
    Pubmed CrossRef
  21. Son, MW, Kim, YJ, Jeong, GA, Cho, GS, and Lee, MS (2014). Long-Term Outcomes of Proximal Gastrectomy versus Total Gastrectomy for Upper-Third Gastric Cancer. J Gastric Cancer. 14, 246-251.
    Pubmed KoreaMed CrossRef
  22. Yoo, CH, Sohn, BH, Han, WK, and Pae, WK (2005). Proximal gastrectomy reconstructed by jejunal pouch interposition for upper third gastric cancer: prospective randomized study. World J Surg. 29, 1592-1599.
    Pubmed CrossRef
  23. Takiguchi, N, Takahashi, M, and Ikeda, M (2015). Long-term quality-of-life comparison of total gastrectomy and proximal gastrectomy by postgastrectomy syndrome assessment scale (PGSAS-45): a nationwide multi-institutional study. Gastric Cancer. 18, 407-416.
    Pubmed CrossRef
  24. Kong, SH, Kim, JW, Lee, HJ, Kim, WH, Lee, KU, and Yang, HK (2010). Reverse double-stapling end-to-end esophagogastrostomy in proximal gastrectomy. Dig Surg. 27, 170-174.
    Pubmed CrossRef
  25. Kitamura, K, Yamaguchi, T, and Nishida, S (1997). The operative indications for proximal gastrectomy in patients with gastric cancer in the upper third of the stomach. Surg Today. 27, 993-998.
    Pubmed CrossRef
  26. Pu, YW, Gong, W, Wu, YY, Chen, Q, He, TF, and Xing, CG (2013). Proximal gastrectomy versus total gastrectomy for proximal gastric carcinoma. A meta-analysis on postoperative complications, 5-year survival, and recurrence rate. Saudi Med J. 34, 1223-1228.
  27. Tokunaga, M, Ohyama, S, and Hiki, N (2008). Endoscopic evaluation of reflux esophagitis after proximal gastrectomy: comparison between esophagogastric anastomosis and jejunal interposition. World J Surg. 32, 1473-1477.
    Pubmed CrossRef
  28. Katsoulis, IE, Robotis, JF, Kouraklis, G, and Yannopoulos, PA (2006). What is the difference between proximal and total gastrectomy regarding postoperative bile reflux into the oesophagus?. Dig Surg. 23, 325-330.
    Pubmed CrossRef
  29. Zhao, P, Xiao, SM, Tang, LC, Ding, Z, Zhou, X, and Chen, XD (2014). Proximal gastrectomy with jejunal interposition and TGRY anastomosis for proximal gastric cancer. World J Gastroenterol. 20, 8268-8273.
    Pubmed KoreaMed CrossRef
  30. Katai, H, Morita, S, Saka, M, Taniguchi, H, and Fukagawa, T (2010). Long-term outcome after proximal gastrectomy with jejunal interposition for suspected early cancer in the upper third of the stomach. Br J Surg. 97, 558-562.
    Pubmed CrossRef
  31. Nakamura, M, Nakamori, M, and Ojima, T (2014). Reconstruction after proximal gastrectomy for early gastric cancer in the upper third of the stomach: an analysis of our 13-year experience. Surgery. 156, 57-63.
    Pubmed CrossRef
  32. Kinoshita, T, Gotohda, N, Kato, Y, Takahashi, S, Konishi, M, and Kinoshita, T (2013). Laparoscopic proximal gastrectomy with jejunal interposition for gastric cancer in the proximal third of the stomach: a retrospective comparison with open surgery. Surg Endosc. 27, 146-153.
  33. Ahn, SH, Jung, DH, Son, SY, Lee, CM, Park, DJ, and Kim, HH (2014). Laparoscopic double-tract proximal gastrectomy for proximal early gastric cancer. Gastric Cancer. 17, 562-570.
  34. Lee, CM, Park, DW, and Jung, DH (2016). Single-Port Laparoscopic Proximal Gastrectomy with Double Tract Reconstruction for Early Gastric Cancer: Report of a Case. J Gastric Cancer. 16, 200-206.
    Pubmed KoreaMed CrossRef
  35. Ando, S, and Tsuji, H (2008). Surgical technique of vagus nerve-preserving gastrectomy with D2 lymphadenectomy for gastric cancer. ANZ J Surg. 78, 172-176.
    Pubmed CrossRef
  36. Kojima, K, Yamada, H, Inokuchi, M, Kawano, T, and Sugihara, K (2008). Functional evaluation after vagus-nerve-sparing laparoscopically assisted distal gastrectomy. Surg Endosc. 22, 2003-2008.
    Pubmed CrossRef
  37. Kim, SM, Cho, J, and Kang, D (2016). A Randomized Controlled Trial of Vagus Nerve-preserving Distal Gastrectomy Versus Conventional Distal Gastrectomy for Postoperative Quality of Life in Early Stage Gastric Cancer Patients. Ann Surg. 263, 1079-1084.
    Pubmed CrossRef
  38. Park, JY, Kim, YW, and Ryu, KW (2016). Assessment of laparoscopic stomach preserving surgery with sentinel basin dissection versus standard gastrectomy with lymphadenectomy in early gastric cancer-A multicenter randomized phase III clinical trial (SENORITA trial) protocol. BMC Cancer. 16, 340.
    Pubmed KoreaMed CrossRef
  39. Valsecchi, ME, Silbermins, D, de Rosa, N, Wong, SL, and Lyman, GH (2011). Lymphatic mapping and sentinel lymph node biopsy in patients with melanoma: a meta-analysis. J Clin Oncol. 29, 1479-1487.
    Pubmed CrossRef
  40. Veronesi, U, Paganelli, G, and Viale, G (2003). A randomized comparison of sentinel-node biopsy with routine axillary dissection in breast cancer. N Engl J Med. 349, 546-553.
    Pubmed CrossRef
  41. Mansel, RE, Fallowfield, L, and Kissin, M (2006). Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J Natl Cancer Inst. 98, 599-609.
    Pubmed CrossRef
  42. Symeonidis, D, Koukoulis, G, and Tepetes, K (2014). Sentinel node navigation surgery in gastric cancer: Current status. World J Gastrointest Surg. 6, 88-93.
    Pubmed KoreaMed CrossRef
  43. Arigami, T, Uenosono, Y, and Yanagita, S (2017). Clinical application and outcomes of sentinel node navigation surgery in patients with early gastric cancer. Oncotarget. 8, 75607-75616.
    Pubmed KoreaMed CrossRef
  44. Park, JY, Ryu, KW, and Eom, BW (2014). Proposal of the surgical options for primary tumor control during sentinel node navigation surgery based on the discrepancy between preoperative and postoperative early gastric cancer diagnoses. Ann Surg Oncol. 21, 1123-1129.
    Pubmed CrossRef
  45. Kitagawa, Y, Takeuchi, H, and Takagi, Y (2013). Sentinel node mapping for gastric cancer: a prospective multicenter trial in Japan. J Clin Oncol. 31, 3704-3710.
    Pubmed CrossRef
  46. Ko, WJ, Song, GW, Kim, WH, Hong, SP, and Cho, JY (2016). Endoscopic resection of early gastric cancer: current status and new approaches. Transl Gastroenterol Hepatol. 1, 24.
    Pubmed KoreaMed CrossRef
  47. Facciorusso, A, Antonino, M, Di Maso, M, and Muscatiello, N (2014). Endoscopic submucosal dissection vs endoscopic mucosal resection for early gastric cancer: A meta-analysis. World J Gastrointest Endosc. 6, 555-563.
    Pubmed KoreaMed CrossRef
  48. Hahn, KY, Park, CH, and Lee, YK (2018). Comparative study between endoscopic submucosal dissection and surgery in patients with early gastric cancer. Surg Endosc. 32, 73-86.
    Pubmed CrossRef
  49. Goto, O, Takeuchi, H, Kitagawa, Y, and Yahagi, N (2016). Hybrid surgery for early gastric cancer. Transl Gastroenterol Hepatol. 1, 26.
    Pubmed KoreaMed CrossRef
  50. Abe, N, Mori, T, and Takeuchi, H (2008). Successful treatment of early stage gastric cancer by laparoscopy-assisted endoscopic full-thickness resection with lymphadenectomy. Gastrointest Endosc. 68, 1220-1224.
    Pubmed CrossRef

This Article

Cited By Articles
  • CrossRef (0)

Author ORCID Information

Social Network Service