Laparoscopic Proximal Gastrectomy and Laparoscopic Subtotal Gastrectomy: History
Please note this is an old version of this entry, which may differ significantly from the current revision.
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Laparoscopic proximal gastrectomy (LPG) and laparoscopic distal gastrectomy with a small remnant stomach, namely laparoscopic subtotal gastrectomy (LsTG), are alternative function-preserving procedures for laparoscopic total gastrectomy (LTG) of early proximal gastric cancer.

  • proximal gastric cancer
  • laparoscopic proximal gastrectomy
  • laparoscopic subtotal gastrectomy

1. Introduction

The survival of patients with early gastric cancer is now so favorable that the preservation of stomach functions to maintain postoperative quality of life (QOL) has become an important issue in the treatment of early gastric cancer [1][2]. Although function-preserving gastrectomy is not strictly defined, maintaining the stomach volume and structures that have specific functions, such as the cardia and the pylorus, is usually described as function-preserving gastrectomy. Laparoscopic total gastrectomy (LTG) is currently the standard procedure for early and even advanced proximal gastric cancer based on the results of some pivotal clinical trials [3][4]. Additionally, laparoscopic proximal gastrectomy (LPG) and laparoscopic distal gastrectomy with a small remnant stomach, namely subtotal gastrectomy (LsTG) [5], are adapted as function-preserving gastrectomy for such disease. Total gastrectomy (TG) may cause postoperative poor QOL because of malnutrition [6]. LPG and LsTG are performed as alternative procedures to maintain postoperative QOL by preserving the stomach volume and the pylorus or cardia.
LPG may be a suitable procedure for early proximal gastric cancer with regard to oncological aspects such as adequate lymph node dissection [7][8]. Furthermore, LPG has possible advantages regarding nutritional intake, including preserving the gastric volume and the pylorus, despite fewer gastric acid and hormone deficiencies. However, no standard reconstructive method for LPG has been established because few of these methods secure the balance between some clinical problems, such as anastomotic stenosis and gastroesophageal reflux.
Although the remnant stomach is extremely small, LsTG is basically a common procedure, with laparoscopic distal gastrectomy (LDG) performed for the transection of the stomach and reconstruction. Thus, it is easy to introduce this procedure instead of LPG. Furthermore, the postoperative outcomes of LsTG are predictable, based on many experiences of LDG. However, whether LsTG is an oncologically and nutritionally acceptable procedure for early proximal gastric cancer compared with LTG or LPG remains unclear.

2. LPG

2.1. Indication of LPG

The Japanese Gastric Cancer Treatment Guidelines (JGCTGs) state that LPG is an alternative procedure to LTG for cT1N0M0 tumors located in the upper third of the stomach regarding QOL and survival outcomes [9]. In LPG, D1+ lymphadenectomy was caried out including dissection of the lymph nodes at station numbers 1, 2 3a, 4sa, 4sb, 7, 8a, 9, and 11p [9]. Nationwide retrospective and prospective studies of lymph node metastasis in EGJ cancer in Japan showed an optimal lymphadenectomy region [10][11]. These studies demonstrated that the incidence of lymph node metastasis around the right gastric and right gastroepiploic artery area was zero to extremely low. Thus, proximal gastrectomy (PG) has a good indication not only for proximal gastric cancer but also for EGJ cancer. Furthermore, several studies also revealed that PG is not a limited procedure for early gastric cancer. According to the JGCTGs, the recommended surgery for upper third of stomach is TG with D2 nodal dissection for advanced disease. However, Ri et al. revealed that the frequencies of lymph node metastasis and therapeutic indices of suprapyloric nodes, infrapyloric nodes, and right greater curvature nodes along the right gastroepiploic artery are significantly low in advanced gastric cancer located in the upper third of the stomach [12]. Therefore, PG may be indicated for advanced gastric cancer in the upper third of the stomach considering the depth, size, and localization, as well as preoperative lymph node metastasis.

2.2. Reconstruction Methods Following LPG

LPG can preserve more than half of the gastric volume and the pylorus, making it an ideal procedure as a function-preserving gastrectomy. However, LPG has the unavoidable problem of losing the cardia. The cardia prevents reflux in cooperation with the adjacent diaphragmatic crus and the phrenoesophageal ligament. After LPG, reconstructive devices to prevent reflux are required; in their absence, the contents of the remnant stomach are easily regurgitated, with specific symptoms such as heart burn, fore-chest pain, vomiting, and aspiration. Although many reconstruction methods for preventing reflux have been developed, a reconstruction method has not been definitively established.
Esophagogastrostomy (EG) and esophagojejunostomy (EJ) are two major methods of reconstruction following LPG. EG is the simplest reconstruction method, but simple anastomotic EG does not avoid reflux. Thus, EG is usually accomplished with anti-reflux techniques. LPG with the double-flap technique (DFT) is one such technique and is currently a preferred reconstruction technique for LPG in Japan. However, double-tract (DT), jejunal interposition (JI), and jejunal pouch interposition are included in EJ after LPG. Among laparoscopic approaches, DT and JI are now common reconstruction methods including EJ.

3. LPG-DFT

Surgical Procedures of LPG-DFT

The DFT was first reported by Kamikawa et al. in 2001 [13], and the detailed surgical procedure of EG with valvuloplasty by the DFT in LPG was described in recent reports [14][15][16]. Briefly, double flaps are created extracorporeally by dissecting between the submucosal and muscular layers on the anterior wall of the remnant stomach. After creating the seromuscular double flaps, the walls of the esophagus and gastric mucosa are sutured under laparoscopic view and an esophagogastrostomy is created. Finally, the hinged flaps are used to laparoscopically cover the anastomosis and lower esophagus.

Outcomes of LPG-DFT

Articles describing LPG-DFT are summarized in Table 1. The incidences of anastomotic stenosis, leakage, and reflux esophagitis were 0–29.1%, 0–7.7%, and 0–10.5%, respectively [14][15][16][17][18][19][20][21][22][23][24]. Furthermore, bodyweight loss (BWL), which may represent a postoperative nutritional outcome, was 8.5–15% [16][17][18][19][20][24]. Kuroda et al. reported the incidence of stenosis in LPG-DFT as 15%, but 5% in open PG with the DFT [14]. Furthermore, Shibasaki et al. reported that the incidence of stenosis was 25% in robot-assisted LPG-DFT [20]. Despite the low incidence of reflux esophagitis and leakage, the high occurrence of stenosis is an important problem of LPG-DFT. Several articles reported the risk of stenosis in LPG-DFT, and Shibasaki et al. presented the negative relationship between stenosis and the total number of stitches [20]. When performing LPG-DFT, an excessive number of stitches should be avoided because of the possibility of stenosis. The incidence of stenosis in LPG-DFT was higher than that in open PG-DFT and may be due to an excessive number of stitches under a magnified visual field of the laparoscopic view, which can lead to ischemia of the anastomosis. Furthermore, many surgeons adopt a continuous suture with a barbed string in LPG-DFT, which is often associated with stenosis. In robotic approaches, the lack of tactile feedback may lead to excessive tightening of stitches. Regarding other aspects, Shoji et al. reported a multivariate analysis that revealed that an esophageal diameter of <18 mm on pre-operative computed tomography images and the presence of short-term complications were independent risk factors for stenosis [25]. Muraoka et al. reported that the incidence of stenosis decreased from 50.0% to 8.3% after adopting intraoperative gastroendoscopy [15]. Considering these results, solutions for stenosis in LPG-DFT may include avoiding excessive stitches, a narrow esophagus, and postoperative complications, as well as using a gastroendoscope as a stent.
Table 1. Summary of LPG-DFT literature.
Another problem of LPG-DFT is the prolonged surgery time resulting from complex intracorporeal anastomotic procedures. The median or mean surgical times of LPG-DFT were more than 6 h in five of the nine published articles [15][16][18][20][21]. To solve such an essential problem, Omori et al. reported LPG-DFT using a stapler, which took a significantly shorter surgical time than conventional hand sewing anastomosis, although the other surgical outcomes such as reflux esophagitis were comparable [24].

LPG-DFT for EGJ Cancer

Although the DFT is a very effective reconstruction method for reflux esophagitis, it is controversial as to whether the DFT is a suitable reconstruction of LPG plus lower esophagectomy for EGJ cancer, which requires mediastinal or intrathoracic anastomosis. Mediastinal anastomosis is very complicated procedure in a limited surgical field, and negative pressure of the intrathoracic cavity may increase the risk of reflux esophagitis. In fact, Kuroda et al. reported that the incidence of reflux esophagitis was 18.2% for grade B or higher in patients whose DFT anastomosis was located in the mediastinum or intrathoracic cavity, and the anastomotic site in the mediastinum or intrathorax was one of the independent risk factors for reflux esophagitis [14]. However, Omori et al. showed that the incidence of reflux esophagitis was 6.9% after LPG plus lower esophagectomy with the DFT using a linear stapler for Siewert type II EGJ cancer [24]. Some modifications of the DFT may be necessary for performing effective DFT in the mediastinum or intrathoracic space.

3.1. LPG-non-DFT

LPG-non-DFT using a circular stapler Table 2 summarizes a literature review of LPG-non-DFT. Most LPG-non-DFT is performed using a circular stapler. EG using a circular stapler is well known to have a high risk of reflux esophagitis in open PG [26][27]. Naturally, some types of techniques to prevent reflux esophagitis have been designed in LPG-non-DFT using a circular stapler [22][28][29][30][31]. However, the incidence of reflux esophagitis was still high, ranging 3.8–31.3% [22][28][29][30][31]. In addition, the incidence of anastomotic stenosis in this procedure ranged 13–27.5% [22][28][29][30][31]. In LPG, EG using a circular stapler may be not suitable for both stenosis and reflux esophagitis, similar to open PG. In LPG-non-DFT using a circular staple, the median or mean surgery times were less than 6 h except in one report [22][29][30][32]. BWL was 10.5–15% in the postoperative period [22][29][30][32].
Table 2. Summary of LPG-non-DFT literature.

3.2. LPG-non-DFT Using a Linear Stapler

Ahn et al. reported that the incidence of stenosis was significantly higher in an end-to-end EG with a circular stapler than in a side-to-side EG with a liner stapler (46.2% vs. 0%, p < 0.001) [33]. Yamashita also reported that side overlap EG using a linear stapler with fundoplication, namely the side overlap with fundoplication by Yamashita (SOFY) method, was effective to avoid stenosis, leakage, and reflux esophagitis in comparison to EG with a circular stapler [32][34]. In the SOFY method, the left side of the esophageal wall is anastomosed with the anterior gastric wall using linear stapler and the right side of the esophageal wall is stuck to the gastric wall, which causes the preserved dorsal esophageal wall to be pressed and flattened into a valvate shape by pressure from the artificial fundus to form the reflux prevention mechanism [32]. Anastomosis using a linear stapler may be a more suitable technique for laparoscopic procedures than that using a circular stapler and is easier than that with an intracorporeal hand sewing suture [36][37]. Hence, anastomosis using a linear stapler that can prevent stenosis and reflux will be a common method for LPG-EG if favorable long-term surgical results are obtained. In LPG-non-DFT using a linear stapler, the median or mean surgery times were less than 6 h [32][34][35]. BWL was 7.4% in the postoperative period [32].

3.3. LPG-DT and JI

Table 3 details a literature review of LPG-DT and JI. The incidences of anastomotic stenosis, leakage, and reflux esophagitis in the DT were reported to be 0–21.4%, 0–10%, and 6.7–25%, respectively [7][23][30][35][38][39][40][41][42][43]. Those in the JI were 0–20%, 0–9.5%, and 0–10%, respectively [28][39][40][44][45]. The incidence of stenosis in EJ was observed at a certain rate for a circular stapler but was 0% for a linear stapler except for one report [7][23][39][40][41][42][43][44][45], while the incidence of stenosis in EJ of LTG with a circular stapler was reported as 7.1–7.7% [46][47]. Thus, EJ with a circular stapler has a risk of stenosis in both LTG and LPG. Recently, EJ was mainly performed with a linear stapler as overlapping or functional end-to-end anastomotic methods. The incidence of stenosis in EJ of LTG using a liner stapler is significantly lower than that using a circular stapler [46][47]. Therefore, the use of a linear stapler in the DT or JI may improve the incidence of stenosis.
In both the DT and JI, the small intestine is cut and lifted to interpose between the esophagus and the stomach to prevent reflux esophagitis. Such usage of the small intestine can induce several issues. One is small bowel obstruction due to adhesion and another is difficulty in performing endoscopic surveillance of the remnant stomach. The incidences of small bowel obstruction and impossible surveillance were reported to be 9.4–20.0% and 7–50%, respectively [28][35][39][41][46][48][49]. In PG, 5.0–9.1% patients experience remnant stomach cancer or newly arisen cancer [50][51]. Hence, the simplicity of postoperative surveillance makes it an important factor in choosing the method of reconstruction following LPG.
Although LPG-DT and JI require multiple anastomoses, the mean or median surgical time was within 6 h in all reports [7][30][35][38][40][41][42][43][44][45]. BWL in LPG-DT and JI was 9.6–12.4% and 8.9%, respectively [7][30][38][39][42][43]. In LPG-DT, there are some patients in whom ingested foods do not pass through the remnant stomach, but the values of BWL were reported to be comparable to the other LPG reconstruction methods.
Table 3. Summary of LPG-DT and JI literature.

4. LsTG

4.1. Specific Features of LsTG

In the early days of laparoscopic procedures, when LPG and LTG surgical results were inadequate, LsTG was first reported in 2011 by Jiang et al. as another procedure for early proximal gastric cancer [5]. The surgical procedure for this approach was described in previous reports [5][18]. Although it is commonly the same procedure as that of conventional LDG, there is the occasional requirement for lymph node dissection along the splenic artery (around the posterior gastric artery) in addition to D1+ lymphadenectomy including dissection of the lymph nodes at station numbers 1, 3a, 3b, 4sb, 5, 6, 7, 8a, and 9, and securing an oral margin by intraoperative endoscopy with intraoperative frozen section analysis is conducted at a different point. In LsTG, securing an oral margin is the most technically essential point. Placement of marking clips and intraoperative endoscopy is effective in determining a gastric transection line for LsTG. Kawakatsu et al. showed that the success rate of achieving a negative surgical margin during the initial transection was 98.9% in patients who underwent preoperative placement of marking clips and intraoperative endoscopy [53]. However, in patients with a proximal tumor extremely close to the cardia or fornix who are eligible for LsTG, conventional marking with clip placement might be problematic because of the risk of wedging by a linear stapler. As a safe technique for securing an oral margin in such patients, Kamiya et al. established that endoscopic cautery marking involving the use of endoscopic forceps cauterization was effective in determining a gastric transection line [54].

4.2. Indication of LsTG

Although LsTG is one procedure for proximal gastric cancer, the indication of LsTG has several limitations. Table 4 shows a literature review of LsTG. In four of the five articles, LsTG was performed for cT1N0 or Stage I disease. LsTG was usually performed in patients who fulfil the following criteria: first, early gastric cancer diagnosed as cT1N0; second, tumor located in or involving the upper third of the stomach; and third, the proximal boundary of the tumor is more than 3 cm from the EGJ. Although the new marking technique described above enables transection of the stomach closer to the cardia, disease that is located extremely close to the EGJ or in the fundus is not an indication for this procedure. Nakauchi et al. reported that the survival of LsTG for advanced gastric cancer was comparable to that of conventional LDG for advanced gastric cancer [55]. However, this is the only report regarding LsTG for advanced gastric cancer. Thus, whether the indication of LsTG for advanced gastric cancer is adequate remains unclear. Furthermore, there are still oncological and nutritional concerns in LsTG for early gastric cancer.
Table 4. Summary of LsTG literature.

4.3. Oncological Problems of LsTG

Regarding the oncological aspects, LsTG is essentially associated with an insufficient proximal margin because of its proximity to the cardia and the risk of inadequate lymph node dissection, especially the left cardial and left greater curvature nodes along the short gastric arteries, despite proximal gastric cancer. Kano et al. reported that LsTG was oncologically feasible for cT1N0M0 gastric cancer located in the upper gastric body because of the extremely low incidence of metastases at such lymph node stations and had 3-year overall survival and relapse-free survival rates equivalent to those of LPG and LTG [59]. However, the length of the proximal margin in LsTG was significantly shorter than those in LPG and LTG. Another aspect of the oncological problem of short proximal margin length is whether the length is associated with survival outcome, which has been controversial [26][60][61][62][63][64]. However, Hayami et al. revealed that shorter proximal margin lengths than the recommendations of the JGCTGs in early gastric cancer did not affect survival outcome [65].

4.4. Nutritional Problems of LsTG

The remnant stomach after LsTG nearly consists of only the cardia and fornix. Whether such an extremely small proximal remnant stomach works effectively for maintaining postoperative nutrition and QOL is another issue of LsTG. Mean or median BWL after LsTG was approximately 10–12%, except for one report that reported 4–6% BWL [18][55][56][57][58]. Compared with LTG or LPG, BWL after LsTG was comparable to that in LPG [18][57], while it was significantly lower than that in LTG [55][56][57]. Furthermore, it is generally assumed that the grade of BWL after LsTG is higher compared with that of conventional LDG. Yasufuku et al. reported that although the difference in BWL between LsTG and conventional LDG was statistically significant, it was only approximately 2% and might not strongly influence the QOL of patients undergoing LsTG [58].
Regarding nutritional parameters at certain times after surgery, Kosuga et al. reported that serum total protein (TP) and albumin (Alb) levels in LsTG were significantly higher than those in LTG [56]. Furukawa et al. reported that LsTG resulted in better serum Alb and prognostic nutritional index levels than LPG, and hemoglobin (Hb) levels in LsTG were significantly higher than in LTG [57]. Yasufuku et al. reported that TP and Alb levels after LsTG were comparable to those in conventional LDG, but Hb levels in LsTG were significantly lower than those in conventional LDG [58]. However, Kano et al. showed that TP, Alb, and Hb levels at 1 year after surgery were comparable between LsTG and LPG-DFT, but Hb levels at 3 years after LsTG were significantly lower than those after LPG-DFT [18].

4.5. Reflux Esophagitis after LsTG

LsTG confers a risk of reflux esophagitis compared with conventional LDG because of the issue of hiatal hernia, which is caused by the destruction of the normal structure around the EGJ in sufficient lymph node dissection. However, the incidence of reflux esophagitis after LsTG was reported to be 0–4% [18][56][57][58], which is feasible compared with that after LPG. In fact, a Japanese multi-center study recently revealed that (L)sTG was associated with better postgastrectomy symptoms including esophageal reflux and daily lives than (L)TG using the Postgastrectomy Syndrome Assessment Scale-45 [66].

5. LPG vs. LsTG

Although both LPG and LsTG are surgeries for cancer in the upper stomach, they are opposite-side procedures. In LPG, the upper stomach is removed and the middle to lower stomach is preserved. Conversely, in LsTG, the middle to lower stomach is completely removed. Thus, indications for both procedures are essentially different. However, the indications sometimes overlap. When a tumor is located in the upper gastric body, both procedures can be performed. In such a case, the surgeon must select which procedure to perform, LPG or LsTG. Table 5 presents the differences between the two procedures according to the current literature [7][14][15][16][17][18][19][20][21][22][23][24][29][30][32][33][34][35][36][37][38][39][40][41][42][43][44][45][55][56][57][58]. The oncological and nutritional outcomes were basically comparable in both procedures. Regarding the resection margin length and anemia as a long-term outcome, LPG was superior to LsTG, although the surgery time of LsTG was shorter than that of LPG.
Table 5. Comparative outcomes of LPG and LsTG.
Surgical Outcome
[7][14][15][16][17][18][19][20][21][22][23][24][29][30][32][33][34][35][36][37][38][39][40][41][42][43][44][45][55][56][57][58]
Oncological Outcome [59] Nutritional Outcome [18][57]
Procedure Time,
min
Anastomotic
Stenosis
Anastomotic
Leakage
Reflux
Esophagitis
PM Length OS TP Alb Hb BWL
LPG 189–389 0–46.2% 0–12.5% 0–31.3% LsTG < LPG LsTG = LPG LsTG = PG LsTG ≥ LPG LsTG ≤ PG LsTG = PG
LsTG 274–333 0–3.5% 0–3% 0–4%
LPG, laparoscopic proximal gastrectomy; LsTG, laparoscopic subtotal gastrectomy; PM, proximal margin; OS, overall survival; TP, total protein; Alb, albumin; Hb, hemoglobin; BWL, body weight loss.

This entry is adapted from the peer-reviewed paper 10.3390/cancers15010311

References

  1. Japanese Gastric Cancer Association Registration Committee; Maruyama, K.; Kaminishi, M.; Hayashi, K.; Isobe, Y.; Honda, I.; Katai, H.; Arai, K.; Kodera, Y.; Nashimoto, A. Gastric cancer treated in 1991 in Japan: Data analysis of nationwide registry. Gastric Cancer 2006, 9, 51–66.
  2. Nakamura, K.; Ueyama, T.; Yao, T.; Xuan, Z.X.; Ambe, K.; Adachi, Y.; Yakeishi, Y.; Matsukuma, A.; Enjoji, M. Pathology and prognosis of gastric carcinoma. Findings in 10,000 patients who underwent primary gastrectomy. Cancer 1992, 70, 1030–1037.
  3. Liu, F.; Huang, C.; Xu, Z.; Su, X.; Zhao, G.; Ye, J.; Du, X.; Huang, H.; Hu, J.; Li, G.; et al. Morbidity and Mortality of Laparoscopic vs. Open Total Gastrectomy for Clinical Stage I Gastric Cancer: The CLASS02 Multicenter Randomized Clinical Trial. JAMA Oncol. 2020, 6, 1590–1597.
  4. Etoh, T.; Honda, M.; Kumamaru, H.; Miyata, H.; Yoshida, K.; Kodera, Y.; Kakeji, Y.; Inomata, M.; Konno, H.; Seto, Y.; et al. Morbidity and mortality from a propensity score-matched, prospective cohort study of laparoscopic versus open total gastrectomy for gastric cancer: Data from a nationwide web-based database. Surg. Endosc. 2018, 32, 2766–2773.
  5. Jiang, X.; Hiki, N.; Nunobe, S.; Nohara, K.; Kumagai, K.; Sano, T.; Yamaguchi, T. Laparoscopy-assisted subtotal gastrectomy with very small remnant stomach: A novel surgical procedure for selected early gastric cancer in the upper stomach. Gastric Cancer 2011, 14, 194–199.
  6. Takiguchi, N.; Takahashi, M.; Ikeda, M.; Inagawa, S.; Ueda, S.; Nobuoka, T.; Ota, M.; Iwasaki, Y.; Uchida, N.; Kodera, Y.; et al. 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 2015, 18, 407–416.
  7. Jung, D.H.; Lee, Y.; Kim, D.W.; Park, Y.S.; Ahn, S.H.; Park, D.J.; Kim, H.H. Laparoscopic proximal gastrectomy with double tract reconstruction is superior to laparoscopic total gastrectomy for proximal early gastric cancer. Surg. Endosc. 2017, 31, 3961–3969.
  8. Ichikawa, D.; Komatsu, S.; Kubota, T.; Okamoto, K.; Shiozaki, A.; Fujiwara, H.; Otsuji, E. Long-term outcomes of patients who underwent limited proximal gastrectomy. Gastric Cancer 2014, 17, 141–145.
  9. Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines 2014 (ver. 4). Gastric Cancer 2017, 20, 1–19.
  10. Kurokawa, Y.; Takeuchi, H.; Doki, Y.; Mine, S.; Terashima, M.; Yasuda, T.; Yoshida, K.; Daiko, H.; Sakuramoto, S.; Yoshikawa, T.; et al. Mapping of Lymph Node Metastasis from Esophagogastric Junction Tumors: A Prospective Nationwide Multicenter Study. Ann. Surg. 2019, 274, 120–127.
  11. Yamashita, H.; Seto, Y.; Sano, T.; Makuuchi, H.; Ando, N.; Sasako, M. Results of a nation-wide retrospective study of lymphadenectomy for esophagogastric junction carcinoma. Gastric Cancer 2017, 20, 69–83.
  12. Ri, M.; Kumagai, K.; Namikawa, K.; Atsumi, S.; Hayami, M.; Makuuchi, R.; Ida, S.; Ohashi, M.; Sano, T.; Nunobe, S. Is proximal gastrectomy indicated for locally advanced cancer in the upper third of the stomach? Ann. Gastroenterol. Surg. 2021, 5, 767–775.
  13. Kamikawa, Y.; Kobayashi, T.; Kamiyama, S.; Satomoto, K. A new procedure of esophagogastrostomy to prevent reflux following proximal gastrectomy. Shoukakigeka 2001, 24, 1053–1060. (In Japanese)
  14. Kuroda, S.; Nishizaki, M.; Kikuchi, S.; Noma, K.; Tanabe, S.; Kagawa, S.; Shirakawa, Y.; Fujiwara, T. Double-Flap Technique as an Antireflux Procedure in Esophagogastrostomy after Proximal Gastrectomy. J. Am. Coll. Surg. 2016, 223, e7–e13.
  15. Muraoka, A.; Kobayashi, M.; Kokudo, Y. Laparoscopy-Assisted Proximal Gastrectomy with the Hinged Double Flap Method. World J. Surg. 2016, 40, 2419–2424.
  16. 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, 1635–1642.
  17. Kuroda, S.; Choda, Y.; Otsuka, S.; Ueyama, S.; Tanaka, N.; Muraoka, A.; Hato, S.; Kimura, T.; Tanakaya, K.; Kikuchi, S.; et al. Multicenter retrospective study to evaluate the efficacy and safety of the double-flap technique as antireflux esophagogastrostomy after proximal gastrectomy (rD-FLAP Study). Ann. Gastroenterol. Surg. 2019, 3, 96–103.
  18. Kano, Y.; Ohashi, M.; Ida, S.; Kumagai, K.; Sano, T.; Hiki, N.; Nunobe, S. Laparoscopic proximal gastrectomy with double-flap technique versus laparoscopic subtotal gastrectomy for proximal early gastric cancer. BJS Open 2020, 4, 252–259.
  19. Tsumura, T.; Kuroda, S.; Nishizaki, M.; Kikuchi, S.; Kakiuchi, Y.; Takata, N.; Ito, A.; Watanabe, M.; Kuwada, K.; Kagawa, S.; et al. Short-term and long-term comparisons of laparoscopy-assisted proximal gastrectomy with esophagogastrostomy by the double-flap technique and laparoscopy-assisted total gastrectomy for proximal gastric cancer. PLoS ONE 2020, 15, e0242223.
  20. Shibasaki, S.; Suda, K.; Nakauchi, M.; Kikuchi, K.; Kadoya, S.; Ishida, Y.; Inaba, K.; Uyama, I. Robotic valvuloplastic esophagogastrostomy using double flap technique following proximal gastrectomy: Technical aspects and short-term outcomes. Surg. Endosc. 2017, 31, 4283–4297.
  21. Saeki, Y.; Tanabe, K.; Yamamoto, Y.; Ohta, H.; Saito, R.; Ohdan, H. Laparoscopic proximal gastrectomy with hinged double flap method using knotless barbed absorbable sutures: A case series. Int. J. Surg. Case Rep. 2018, 51, 165–169.
  22. Hosoda, K.; Washio, M.; Mieno, H.; Moriya, H.; Ema, A.; Ushiku, H.; Watanabe, M.; Yamashita, K. Comparison of double-flap and OrVil techniques of laparoscopy-assisted proximal gastrectomy in preventing gastroesophageal reflux: A retrospective cohort study. Langenbecks Arch. Surg. 2019, 404, 81–91.
  23. Saze, Z.; Kase, K.; Nakano, H.; Yamauchi, N.; Kaneta, A.; Watanabe, Y.; Hanayama, H.; Hayase, S.; Momma, T.; Kono, K. Functional benefits of the double flap technique after proximal gastrectomy for gastric cancer. BMC Surg. 2021, 21, 392.
  24. Omori, T.; Yamamoto, K.; Yanagimoto, Y.; Shinno, N.; Sugimura, K.; Takahashi, H.; Yasui, M.; Wada, H.; Miyata, H.; Ohue, M.; et al. A Novel Valvuloplastic Esophagogastrostomy Technique for Laparoscopic Transhiatal Lower Esophagectomy and Proximal Gastrectomy for Siewert Type II Esophagogastric Junction Carcinoma-the Tri Double-Flap Hybrid Method. J. Gastrointest. Surg. 2021, 25, 16–27.
  25. Shoji, Y.; Nunobe, S.; Ida, S.; Kumagai, K.; Ohashi, M.; Sano, T.; Hiki, N. Surgical outcomes and risk assessment for anastomotic complications after laparoscopic proximal gastrectomy with double-flap technique for upper-third gastric cancer. Gastric Cancer 2019, 22, 1036–1043.
  26. Kim, J.; Park, S.; Kim, J.; Boo, Y.; Kim, S.; Mok, Y.; Kim, C. Surgical outcomes for gastric cancer in the upper third of the stomach. World J. Surg. 2006, 30, 1870–1876.
  27. An, J.Y.; Youn, H.G.; Choi, M.G.; Noh, J.H.; Sohn, T.S.; Kim, S. The difficult choice between total and proximal gastrectomy in proximal early gastric cancer. Am. J. Surg. 2008, 196, 587–591.
  28. Yasuda, A.; Yasuda, T.; Imamoto, H.; Kato, H.; Nishiki, K.; Iwama, M.; Makino, T.; Shiraishi, O.; Shinkai, M.; Imano, M.; et al. A newly modified esophagogastrostomy with a reliable angle of His by placing a gastric tube in the lower mediastinum in laparoscopy-assisted proximal gastrectomy. Gastric Cancer 2015, 18, 850–858.
  29. Kosuga, T.; Ichikawa, D.; Komatsu, S.; Okamoto, K.; Konishi, H.; Shiozaki, A.; Fujiwara, H.; Otsuji, E. Feasibility and Nutritional Benefits of Laparoscopic Proximal Gastrectomy for Early Gastric Cancer in the Upper Stomach. Ann. Surg. Oncol. 2015, 22 (Suppl. S3), S929–S935.
  30. 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, 4848–4856.
  31. Toyomasu, Y.; Ogata, K.; Suzuki, M.; Yanoma, T.; Kimura, A.; Kogure, N.; Yanai, M.; Ohno, T.; Mochiki, E.; Kuwano, H. Restoration of gastrointestinal motility ameliorates nutritional deficiencies and body weight loss of patients who undergo laparoscopy-assisted proximal gastrectomy. Surg. Endosc. 2017, 31, 1393–1401.
  32. Yamashita, Y.; Yamamoto, A.; Tamamori, Y.; Yoshii, M.; Nishiguchi, Y. Side overlap esophagogastrostomy to prevent reflux after proximal gastrectomy. Gastric Cancer 2017, 20, 728–735.
  33. Ahn, S.H.; Lee, J.H.; Park, D.J.; Kim, H.H. Comparative study of clinical outcomes between laparoscopy-assisted proximal gastrectomy (LAPG) and laparoscopy-assisted total gastrectomy (LATG) for proximal gastric cancer. Gastric Cancer 2013, 16, 282–289.
  34. Yamashita, Y.; Tatsubayashi, T.; Okumura, K.; Miyamoto, T.; Ueno, K. Modified side overlap esophagogastrostomy after laparoscopic proximal gastrectomy. Ann. Gastroenterol. Surg. 2022, 6, 594–599.
  35. Sakuramoto, S.; Yamashita, K.; Kikuchi, S.; Futawatari, N.; Katada, N.; Moriya, H.; Hirai, K.; Watanabe, M. Clinical experience of laparoscopy-assisted proximal gastrectomy with Toupet-like partial fundoplication in early gastric cancer for preventing reflux esophagitis. J. Am. Coll. Surg. 2009, 209, 344–351.
  36. 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, 3664–3672.
  37. Komatsu, S.; Kubota, T.; Kumano, T.; Okamoto, K.; Ichikawa, D.; Shioaki, Y.; Otsuji, E. Non-flap hand-sewn esophagogastrostomy as a simple anti-reflux procedure in laparoscopic proximal gastrectomy for gastric cancer. Langenbecks Arch. Surg. 2020, 405, 541–549.
  38. Ahn, S.H.; Jung, D.H.; Son, S.Y.; Lee, C.M.; Park, D.J.; Kim, H.H. Laparoscopic double-tract proximal gastrectomy for proximal early gastric cancer. Gastric Cancer 2014, 17, 562–570.
  39. Nomura, E.; Lee, S.W.; Kawai, M.; Yamazaki, M.; Nabeshima, K.; Nakamura, K.; Uchiyama, K. Functional outcomes by reconstruction technique following laparoscopic proximal gastrectomy for gastric cancer: Double tract versus jejunal interposition. World J. Surg. Oncol. 2014, 12, 20.
  40. Nomura, E.; Kayano, H.; Lee, S.W.; 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.
  41. Cho, M.; Son, T.; Kim, H.I.; Noh, S.H.; Choi, S.; Seo, W.J.; Roh, C.K.; Hyung, W.J. Similar hematologic and nutritional outcomes after proximal gastrectomy with double-tract reconstruction in comparison to total gastrectomy for early upper gastric cancer. Surg. Endosc. 2019, 33, 1757–1768.
  42. 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, 3270–3276.
  43. Xiao, S.M.; Zhao, P.; Ding, Z.; Xu, R.; Yang, C.; Wu, X.T. Laparoscopic proximal gastrectomy with double-tract reconstruction for upper third gastric cancer. BMC Surg. 2021, 21, 140.
  44. Kinoshita, T.; Gotohda, N.; Kato, Y.; Takahashi, S.; Konishi, M.; Kinoshita, T. Laparoscopic proximal gastrectomy with jejunal interposition for gastric cancer in the proximal third of the stomach: A retrospective comparison with open surgery. Surg. Endosc. 2013, 27, 146–153.
  45. Takayama, Y.; Kaneoka, Y.; Maeda, A.; Fukami, Y.; Onoe, S. Comparison of outcomes of laparoscopy-assisted and open proximal gastrectomy with jejunal interposition for early gastric cancer in the upper third of the stomach: A retrospective observational study. Asian J. Endosc. Surg. 2018, 11, 329–336.
  46. Murakami, K.; Obama, K.; Tsunoda, S.; Hisamori, S.; Nishigori, T.; Hida, K.; Kanaya, S.; Satoh, S.; Manaka, D.; Yamamoto, M.; et al. Linear or circular stapler? A propensity score-matched, multicenter analysis of intracorporeal esophagojejunostomy following totally laparoscopic total gastrectomy. Surg. Endosc. 2020, 34, 5265–5273.
  47. Lee, S.; Lee, H.; Song, J.H.; Choi, S.; Cho, M.; Son, T.; Kim, H.I.; Hyung, W.J. Intracorporeal esophagojejunostomy using a linear stapler in laparoscopic total gastrectomy: Comparison with circular stapling technique. BMC Surg. 2020, 20, 100.
  48. Tokunaga, M.; Ohyama, S.; Hiki, N.; Hoshino, E.; Nunobe, S.; Fukunaga, T.; Seto, Y.; Yamaguchi, T. Endoscopic evaluation of reflux esophagitis after proximal gastrectomy: Comparison between esophagogastric anastomosis and jejunal interposition. World J. Surg. 2008, 32, 1473–1477.
  49. 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, 558–564.
  50. Nozaki, I.; Kurita, A.; Nasu, J.; Kubo, Y.; Aogi, K.; Tanada, M.; Takashima, S. Higher incidence of gastric remnant cancer after proximal than distal gastrectomy. Hepato-Gastroenterology 2007, 54, 1604–1608.
  51. Katai, H.; Morita, S.; Saka, M.; Taniguchi, H.; Fukagawa, T. Long-term outcome after proximal gastrectomy with jejunal interposition for suspected early cancer in the upper third of the stomach. Br. J. Surg. 2010, 97, 558–562.
  52. Park, J.Y.; Park, K.B.; Kwon, O.K.; 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, 1963–1970.
  53. Kawakatsu, S.; Ohashi, M.; Hiki, N.; Nunobe, S.; Nagino, M.; Sano, T. Use of endoscopy to determine the resection margin during laparoscopic gastrectomy for cancer. Br. J. Surg. 2017, 104, 1829–1836.
  54. Kamiya, S.; Ohashi, M.; Ida, S.; Kumagai, K.; Nunobe, S.; Sano, T.; Hiki, N. Laparoscopic subtotal gastrectomy with a new marking technique, endoscopic cautery marking: Preservation of the stomach in patients with upper early gastric cancer. Surg. Endosc. 2018, 32, 4681–4687.
  55. Nakauchi, M.; Suda, K.; Nakamura, K.; Shibasaki, S.; Kikuchi, K.; Nakamura, T.; Kadoya, S.; Ishida, Y.; Inaba, K.; Taniguchi, K.; et al. Laparoscopic subtotal gastrectomy for advanced gastric cancer: Technical aspects and surgical, nutritional and oncological outcomes. Surg. Endosc. 2017, 31, 4631–4640.
  56. Kosuga, T.; Hiki, N.; Nunobe, S.; Noma, H.; Honda, M.; Tanimura, S.; Sano, T.; Yamaguchi, T. Feasibility and nutritional impact of laparoscopy-assisted subtotal gastrectomy for early gastric cancer in the upper stomach. Ann. Surg. Oncol. 2014, 21, 2028–2035.
  57. Furukawa, H.; Kurokawa, Y.; Takiguchi, S.; Tanaka, K.; Miyazaki, Y.; Makino, T.; Takahashi, T.; Yamasaki, M.; Nakajima, K.; Mori, M.; et al. 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, 500–507.
  58. Yasufuku, I.; Ohashi, M.; Eto, K.; Ida, S.; Kumagai, K.; Nunobe, S.; Sano, T.; Hiki, N. Size-dependent diferences in the proximal remnant stomach: How much does a small remnant stomach after subtotal gastrectomy work? Surg. Endosc. 2020, 34, 5540–5549.
  59. Kano, Y.; Ohashi, M.; Ida, S.; Kumagai, K.; Nunobe, S.; Sano, T.; Hiki, N. Oncological feasibility of laparoscopic subtotal gastrectomy compared with laparoscopic proximal or total gastrectomy for cT1N0M0 gastric cancer in the upper gastric body. Gastric Cancer 2019, 22, 1060–1068.
  60. Berlth, F.; Kim, W.H.; Choi, J.H.; Park, S.H.; Kong, S.H.; Lee, H.J.; Yang, H.K. Prognostic Impact of Frozen Section Investigation and Extent of Proximal Safety Margin in Gastric Cancer Resection. Ann. Surg. 2020, 272, 871–878.
  61. Ohe, H.; Lee, W.Y.; Hong, S.W.; Chang, Y.G.; Lee, B. Prognostic value of the distance of proximal resection margin in patients who have undergone curative gastric cancer surgery. World J. Surg. Oncol. 2014, 12, 296.
  62. Postlewait, L.M.; Squires, M.H., 3rd; Kooby, D.A.; Poultsides, G.A.; Weber, S.M.; Bloomston, M.; Fields, R.C.; Pawlik, T.M.; Votanopoulos, K.I.; Schmidt, C.R.; et al. The importance of the proximal resection margin distance for proximal gastric adenocarcinoma: A multi-institutional study of the US Gastric Cancer Collaborative. J. Surg. Oncol. 2015, 112, 203–207.
  63. Squires, M.H., 3rd; Kooby, D.A.; Poultsides, G.A.; Pawlik, T.M.; Weber, S.M.; Schmidt, C.R.; Votanopoulos, K.I.; Fields, R.C.; Ejaz, A.; Acher, A.W.; et al. Is it time to abandon the 5-cm margin rule during resection of distal gastric adenocarcinoma? A multi-institution study of the U.S. Gastric Cancer Collaborative. Ann. Surg. Oncol. 2015, 22, 1243–1251.
  64. Mine, S.; Sano, T.; Hiki, N.; Yamada, K.; Kosuga, T.; Nunobe, S.; Yamaguchi, T. Proximal margin length with transhiatal gastrectomy for Siewert type II and III adenocarcinomas of the oesophagogastric junction. Br. J. Surg. 2013, 100, 1050–1054.
  65. Hayami, M.; Ohashi, M.; Ishizuka, N.; Hiki, N.; Kumagai, K.; Ida, S.; Sano, T.; Nunobe, S. Oncological Impact of Gross Proximal Margin Length in Distal Gastrectomy for Gastric Cancer: Is the Japanese Recommendation Valid? Ann. Surg. Open 2021, 2, e036.
  66. Nunobe, S.; Takahashi, M.; Kinami, S.; Fujita, J.; Suzuki, T.; Suzuki, A.; Tanahashi, T.; Kawaguchi, Y.; Oshio, A.; Nakada, K. Evaluation of postgastrectomy symptoms and daily lives of small remnant distal gastrectomy for upper-third gastric cancer using a large-scale questionnaire survey. Ann. Gastroenterol. Surg. 2021, 6, 355–365.
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