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Acta Bio Medica : Atenei Parmensis logoLink to Acta Bio Medica : Atenei Parmensis
. 2018;89(Suppl 8):110–116. doi: 10.23750/abm.v89i8-S.7897

Advanced gastric cancer: the value of surgery

Fugazzola Paola 1, Ansaloni Luca 1, Sartelli Massimo 2, Catena Fausto 3, Cicuttin Enrico 1, Leandro Gioacchino 5, Luigi de’Angelis Gian 4, Gaiani Federica 4, Di Mario Francesco 4, Tomasoni Matteo 1, Coccolini Federico 1,
PMCID: PMC6502221  PMID: 30561428

Abstract

Gastric cancer is a common disease with high mortality. The definition of advanced gastric cancer is still debated. Radical surgery associated to appropriate systemic and intra-abdominal chemotherapy is the gold standard treatment. In presence of peritoneal carcinosis, reaching a complete cytoreduction is the key to achieve long-term survival. Adequate lymphadenectomy is also fundamental. Conversion therapy could be applied to selected IV stage patients. No definitive evidences exist regarding the oncological and surgical superiority of mini-invasive approaches over the classical open techniques. (www.actabiomedica.it)

Keywords: advanced gastric cancer; chemotherapy; hipec; intraperitoneal; surgery; definition,metastasis; carcinosis

Introduction

Gastric cancer (GC) is the fifth cause of cancer death in the world. Some differences exist according to the geographic area. Eastern countries have a better prognosis in the treatment of these patients when compared to western. In Japan the survival for resectable GC is almost 70% (1), while in Europe and US the 5-year survival is almost 25% in advanced gastric cancer (AC) (2-6).

The TNM classification of the American Joint Committee on Cancer (AJCC) and Union for International Cancer Control (UICC) is widely used, even if with some criticisms (7-9).

However, precise definition of AC is still matter of debate. Some authors defined as AC the T3 and T4 cancers. As a counterpart, the vast majority considers advanced those tumors infiltrating beyond the submucosal layer that are not-early and not-metastatic even with N0 staging. Practically, AC could be considered the T2-T4b/N0-N3b/M0 according to the AJCC/UICC TNM classification. In addition the proposal of esophagogastric junction cancers classification to replace the Siewert one raised many concerns. Recently the new TNM 8th classification of neoplastic diseases redefined the classification of the gastric and gastro-esophageal junction cancers (GEJC) and formally included the GEJC among the gastric cancers (10). A meta-analysis confirmed the same biological behavior of the GEJC and the AC. The main difference is the anatomical diffusion due to the localization, to the different anatomy of the two regions and the consequent lymphatic drainage (11).

Extension of gastric resection

Radical surgery including adequate resection and lymphadenectomy is the only curative treatment either for early stage either for advanced but non-metastatic disease. Lymphadenectomy could be considered adequate with the retrieval of at least 16 lymph nodes (12).

The recommended oncologically correct proximal margins are: at least 3 cm for T2 or higher degree tumors with “expansive growth pattern” and at least 5 cm in “infiltrative growth pattern” diseases. The concept of adequacy of surgical resection has been defined as total gastrectomy for large tumors or for tumors of the lesser curve and in general in all those situations in which resection margins cannot be respected.

Lymphadenectomy

Besides the penetration of the serosa, the principal factors strongly related with prognosis are the lymph node (LN) involvement (13) and the clearance of lymph nodes (14-16).

As a matter of fact lymphadenectomy is important in staging and in increasing the long-term survival (5, 13). Eastern and western countries use different standard to regulate the extension of the lymphadenectomy. In “standard lymphadenectomy” (D1) almost 15-18 lymph nodes (LN) must be removed to have a proper staging. In “extended lymphadenectomy” (over-D1) the number of LD to remove is 31-35 to have a better staging of the N3 (according to the TNM) and to increase survival (17-20). In D2 lymphadenectomy at least 27 LN should be retrieved for optimal results (19). In Europe, the state-of-the-art in curative-intent surgery for AC is gastrectomy, D2 lymphadenectomy and omentectomy (5, 13, 15, 21-23).

Extent of lymphadenectomies

  • D1 lymphadenectomy includes the peri-gastric stations (from station 1 to 7) (5, 24). When facing esophageal-gastric junction tumors also the infradiaphragmatic, paraesophageal and supradiaphragmatic LN stations (19, 20, 110 and 111 LN stations) should be resected for D1 lymphadenectomy (5).

  • “D1 plus” lymphadenectomy consists in the resection of the stations 8a, 9, and 11p too (25).

  • D2 lymphadenectomy consists in the D1 resection associated to stations 10, 11d, and 12a (5, 25).

  • D3 lymphadenectomy includes also the posterior (12p, 13, 14v) and para-aortic station (26).

  • Super-extender D3 lymphadenectomy includes splenectomy or distal pancreatectomy associated to D2 lymphadenectomy.

At least 16 LN should be retrieved for accurate pathologic evaluation. Some data suggested no increase in accuracy of pN staging with an increase of LN retrieval (27).

D1 vs D2 vs D3 lymphadenectomy

In T1a tumor not suitable for endoscopic resection and for differentiated and ≤1.5 cm cT1bN0 lesions D1 lymphadenectomy is indicated (25). A “D1 plus” lymphadenectomy has been reported as an alternative of D2 in high-risk cT1N0. D2 lymphadenectomy is indicated for potentially curable T2–T4 tumors, as well cT1N + tumors (25). Two randomized controlled trials (RCTs) (18, 28, 29) reported a superiority of the D1 compared with D2 lymphadenectomy. However, no other studies confirmed these results (22, 23, 30). The Italian Gastric Cancer Study Group (GIRCG) showed that D2 dissection without splenectomy and pancreatic resection is feasible and safe with similar results to D1 (22). Some data from a randomized trial (18, 31) showed an increased survival rate in patients who underwent D2 vs. D1, where gastric-cancer-related death and a regional recurrence were higher in D1. Another RCT (25) comparing the difference between D1 plus and D2 showed higher LN removal in D2 lymphadenectomy, no differences in LN ratio, no significant differences in median recurrence rate.

D3 lymphadenectomy is supposed to provide a better local control of disease in advanced gastric tumors with mixed-diffuse histotype (32). As in upper third GC 29% of para-aortic LN are involved compared to the 7% of middle and lower third GC (p<0.001), the inclusion of para-aortic LN stations (16a, 16b) is important in upper third tumors, in larger tumors, or in tumor with station 7 involvement (33, 34). No benefit in survival rate is related to routine extended lymphadenectomy and removal of para-aortic LN (35, 36).

Super-extender D3 lymphadenectomy is strongly not recommended and is in the most of cases not necessary (13, 16, 37-39). Even in scenarios of higher risk for splenic hilum node involvement, i.e., with proximal and mid greater curvature primaries, spleen-preserving hilum lymphadenectomy can be performed with satisfactory results (40). Splenectomy and pancreatectomy might be considered beneficial only in case the primary tumor or the LN metastasis involve these organs (16, 39).

The evaluation of the possible role of an extended lymphadenectomy in reducing the risk of a local recurrence has been reported in several studies (32, 34, 41-43).

Patients who underwent a D2 with para-aortic LN dissection (PAND) presented better outcome in terms of mortality and morbidity, compared to the only D2 have been reported (21). However, another study (34) reported that D2 with PAND has no improving in survival or recurrence rate in T2-subserosa, T3, T4 stages with similar perioperative mortality and an increase in morbidity for the D2 PAND group.

Wu et al. found in a RCT (41) evaluating D1 vs. D3 that morbidity rate was higher in D3 and overall survival was significantly higher and regional recurrence rate lower in D3 (35). De Manzoni reported a higher recurrence rate in D3 group in case of intestinal pattern then in mixed/diffuse pattern with a similar mortality thus emphasizing the necessity to tailor lymphadenectomy to the histology (32).

Cytoreductive surgery

In the event of local or diffuse peritoneal carcinosis (PC) the best approach combines systemic chemotherapy, radical surgery and intra-peritoneal chemotherapy (IPC). This multimodal treatment radically changed the outcomes (44-48).

Differently from ovarian cancer as well as for other diseases (49, 50) in GC with PC, cytoreductive surgery (CRS) alone is not accompanied by survival benefits. As showed by Yamamura et al. CRS alone cannot be effective in treating PC because of invisible cancer cells remain even after surgical procedure. As a counterpart, CRS plus peri-operative chemotherapy is feasible and safe with a significant increase in survival rate in GC with PC (51-54). Furthermore, a meta-analysis clearly showed a survival benefit in patients affected by advanced GC, with or without PC, treated with IPC (44). An independent favourable prognostic factor during CRS if associated to IPC is the completeness of cytoreduction (52, 55-57). A recent meta-analysis reported an increase in 1, 2, 3, and 5-years survival rate in CC-0/CC-1 cytoreduction (58) and CC-0 showed better outcomes than CC-1 with an increased survival at 1 and 3 years. The Peritoneal Cancer Index (PCI) evaluation is mandatory in selecting patients for CRS+IPC treatment. Yonemura et al. showed that it was possible to obtain a complete cytoreduction in 91% of cases in presence of a PCI≤6 but only in 42% with a PCI≥7. Moreover, the survival rate in PCI score ≤6 was significantly better than in PCI score ≥7 (45). Survival rates at different time points change significantly above and below a PCI of 12 with a progressive decrease for higher PCI scores (57, 59-61.

Surgery for IV stage gastric cancer

Chemotherapy remains the main therapeutic approach for stage IV GC and surgery is usually confined to a palliative resection or by-pass operation to relieve symptoms. However, the median survival time of this cohort of patients remains to be around 13-16 months (62). Furthermore, the REGATTA trial demonstrated that the initial removal of the primary tumor in stage IV GC could be beneficial just in case of only one affected organ other than the site of primary tumor (63).

Stage IV GC patients are heterogeneous and could be divided into four categories (62) (64):

  • - Category 1: absence of macroscopic PC and potentially resectable metastases

  • - Category 2: absence of macroscopic PC and marginally resectable metastases

  • - Category 3: presence of macroscopic PC without other distant metastases

  • - Category 4: presence of macroscopic PC and other organ metastases.

According to recent studies, patients in category 1 could be eligible for neoadjuvant chemotherapy and subsequent gastrectomy plus metastasectomy. For the other categories, much attention is being paid to conversion therapy. It is defined as a surgical treatment aiming at an R0 resection after chemotherapy for tumors that were originally unresectable for technical or oncological reasons (64). In a study on 259 patients with IV stage GC, planned resection after neoadjuvant chemotherapy was performed in 7 patients and conversion surgery in 77. Although only 51,2% of patients underwent R0 resection, median survival time was 41.3 months, that is much longer than that reported from the first-line chemotherapy trials (62). Metastasectomy along with resection of the primary tumor might be feasible for this population, once the metastases have responded well to the chemotherapy. Some authors recommend the surgical treatment of hepatic metastases from gastric cancer to be taken into consideration after careful evaluation of each single case, as only a radical approach with curative intent is worthy (65).

Mini-invasive surgical approach

Although studies about mini-invasive surgical approach mixed AC and early gastric cancer patients exist, no dedicated studies to AC were conducted. Results however suggest the possibility to apply the mini-invasive approach to AC without PC.

Laparoscopic surgery

In early gastric cancer laparoscopic resections associated to D1 lymphadenectomy obtained better results than open technique in terms of postoperative pain, time to return to normal bowel function and resumption of oral feeding, time to recovery, length of hospital stay, cosmetic results and financial outcome (66-69). Morbidity and mortality rates in laparoscopy are not statistically different to open resections (29) (22, 70). The role of laparoscopy in D2 or higher for lymphadenectomy is still matter of debate. According to some authors, laparoscopy reduces the accuracy in dissecting lymph nodes, especially from high risk nodal stations. Wang et al. in a meta-analysis including 17 trials (2313 patients) comparing laparoscopic and open total gastrectomy (71) demonstrated a longer operative time, earlier hospital discharge, earlier passage of flatus, quicker resumption of oral intake, fewer analgesic uses, and reduced postoperative morbidity in laparoscopic approach. No difference was found in terms of hospital mortality, resected lymph nodes, proximal resection margin and 5-year overall and disease-free survival. Another meta-analysis of 15 non-randomized trails substantially confirmed the outcomes (72).

Robotic surgery

No sufficient data exist about feasibility, safety and eventual advantages of robotic gastrectomy compared to open or laparoscopic gastrectomy in early gastric cancer neither in AC. No reports exist about the use of robotic gastrectomy in patients with AC and PC.

Liao et al. published a meta-analysis of 4 studies (5780 patients) comparing robotic and open gastrectomy. Longer operation time, lower blood loss and shorter hospital stay were associated to robotic gastrectomy. Overall morbidity and number of resected lymph nodes were not different (73).

Conclusions

Therapeutic approach of AC is based on radical surgery with adequate lymphadenectomy, associated to appropriate systemic and intra-abdominal chemotherapy. In presence of PC reaching a complete removal of visible disease is even more important. In stage IV GC conversion therapy could be considered in selected patients with good response to chemotherapy. No definitive evidences exist regarding the oncological and surgical superiority of the mini-invasive approach over the classical open technique.

References

  • 1.World Health Organization. GLOBOCAN 2012: Estimated Cancer Incidence, Mortality and Prevalence Worldwide. 2012 [Google Scholar]
  • 2.Karimi P, Islami F, Anandasabapathy S, Freedman ND, Kamangar F. Gastric cancer: descriptive epidemiology, risk factors, screening, and prevention. Cancer Epidemiol Biomarkers Prev. 2014;23:700–713. doi: 10.1158/1055-9965.EPI-13-1057. [PMID: 24618998 DOI: 10.1158/1055-9965] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Bauer K, Schroeder M, Porzsolt F, Henne-Bruns D. Comparison of international guidelines on the accompanying therapy for advanced gastric cancer: reasons for the differences. J Gastric Cancer. 2015 Mar;15(1):10–8. doi: 10.5230/jgc.2015.15.1.10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Wang J, Sun Y, Bertagnolli MM. Comparison of Gastric Cancer Survival Between Caucasian and Asian Patients Treated in the United States: Results from the Surveillance Epidemiology and End Results (SEER) Database. Ann Surg Oncol. 2015 Jan 29 doi: 10.1245/s10434-015-4388-4. [DOI] [PubMed] [Google Scholar]
  • 5.Japanese Gastric Cancer Association. Japanese Classification of Gastric Carcinoma ℃ 3nd English Edition. Gastric Cancer. 2011 Jun;14(2):101–12. doi: 10.1007/s10120-011-0041-5. [DOI] [PubMed] [Google Scholar]
  • 6.Verlato G, Giacopuzzi S, Bencivenga M, Morgagni P, De Manzoni G. Problems faced by evidence-based medicine in evaluating lymphadenectomy for gastric cancer. World J Gastroenterol. 2014 Sep 28;20(36):12883–91. doi: 10.3748/wjg.v20.i36.12883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Washington K. 7th edition of the AJCC cancer staging manual: stomach. Ann Surg Oncol. 2010;17:3077–3079. doi: 10.1245/s10434-010-1362-z. [PMID: 20882416 DOI: 10.1245/s10434-010-1362-z] [DOI] [PubMed] [Google Scholar]
  • 8.Sobin LH, Gospodarowicz MK, Wittekind C. International Union Against Cancer (UICC) TNM Classification of Malignant Tumors. 7th ed. New York: Wiley-Liss; 2010 [Google Scholar]
  • 9.Qiu MZ, Wang ZQ, Zhang DS, Liu Q, Luo HY, Zhou ZW, Li YH, Jiang WQ, Xu RH. Comparison of 6th and 7th AJCC TNM staging classification for carcinoma of the stomach in China. Ann Surg Oncol. 2011;18:1869–1876. doi: 10.1245/s10434-010-1542-x. [DOI] [PubMed] [Google Scholar]
  • 10.Ajani JA, In H, Sano T, et al. Stomach, Amin MB E. AJCC Cancer Staging Manual, eighth ed. 2017 [Google Scholar]
  • 11.Coccolini F, Nardi M, Montori G, Ceresoli M, Celotti A, Cascinu S, Fugazzola P, Tomasoni M, Glehen O, Catena F, Yonemura Y, Ansaloni L. Neoadjuvant chemotherapy in advanced gastric and esophago-gastric cancer. Meta-analysis of randomized trials. Int J Surg. 2018 Mar;51:120–127. doi: 10.1016/j.ijsu.2018.01.008. doi: 10.1016/j.ijsu.2018.01.008. Epub 2018 Feb 20. Review. [DOI] [PubMed] [Google Scholar]
  • 12.Seevaratnam R, Bocicariu A, Cardoso R, Yohanathan L, Dixon M, Law C, Helyer L, Coburn NG. How many lymph nodes should be assessed in patients with gastric cancer? A systematic review. Gastric Cancer. 2012;15:S70–88. doi: 10.1007/s10120-012-0169-y. [DOI] [PubMed] [Google Scholar]
  • 13.McCulloch P1, Niita ME, Kazi H, Gama-Rodrigues JJ. Gastrectomy with extended lymphadenectomy for primary treatment of gastric cancer. Br J Surg. 2005 Jan;92(1):5–13. doi: 10.1002/bjs.4839. [DOI] [PubMed] [Google Scholar]
  • 14.Deng J, Zhang R, Pan Y, Wang B, Wu L, Jiao X, Bao T, Hao X, Liang H. Comparison of the staging of regional lymph nodes using the sixth and seventh editions of the tumor-node-metastasis (TNM) classification system for the evaluation of overall survival in gastric cancer patients. Surgery. 2014 Jul;156(1):64–74. doi: 10.1016/j.surg.2014.03.020. [DOI] [PubMed] [Google Scholar]
  • 15.Schwarz RE. Current status of management of malignant disease: current management of gastric cancer. J Gastrointest Surg. 2015 Apr;19(4):782–8. doi: 10.1007/s11605-014-2707-x. [DOI] [PubMed] [Google Scholar]
  • 16.Jiang L, Yang KH, Chen Y, Guan QL, Zhao P, Tian JH, Wang Q. Systematic review and meta-analysis of the effectiveness and safety of extended lymphadenectomy in patients with resectable gastric cancer. Br J Surg. 2014 May;101(6):595–604. doi: 10.1002/bjs.9497. [DOI] [PubMed] [Google Scholar]
  • 17.Siewert JR, Bottcher K, Roder JD, et al. Prognostic relevance of systematic lymph node dissection in gastric carcinoma. Br J Surg. 1993;80:1015–1018. doi: 10.1002/bjs.1800800829. [DOI] [PubMed] [Google Scholar]
  • 18.Bonenkamp JJ, Hermans J, Sasako M, van de Velde CJH. for the Dutch Gastric Cancer Group. Extended lymph-node dissection for gastric cancer. N Engl J Med. 1999;340(12):908–14. doi: 10.1056/NEJM199903253401202. [DOI] [PubMed] [Google Scholar]
  • 19.Wagner PK, Ramaswamy A, Rueschoff J, et al. Lymph node count in the upper abdomen: anatomical basis for lymphadenectomy in gastric cancer. Br J Surg. 1991;78:825–827. doi: 10.1002/bjs.1800780719. [DOI] [PubMed] [Google Scholar]
  • 20.Bozzetti F. Principles of surgical radicality in the treatment of gastric cancer. N Engl J Med. 1999 Mar 25;340(12):908–14. [Google Scholar]
  • Extended lymph-node dissection for gastric cancer. Surg Oncol N Am. 2001;10:833–854. [Google Scholar]
  • 21.Kulig J, Popiela T, Kolodziejczyk P, Sierzega M, Szczepanik A and Group. Polish Gastric Cancer Study. Standard D2 versus extended D2 (D2+) lymphadenectomy for gastric cancer: an interim safety analysis of a multicenter, randomized, clinical trial. Am J Surg. 2007 Jan;193(1):10–5. doi: 10.1016/j.amjsurg.2006.04.018. [DOI] [PubMed] [Google Scholar]
  • 22.Degiuli M, Sasako M, Ponti A, Soldati T, Danese F, Calvo F. Morbidity and mortality after D2 gastrectomy for gastric cancer: results of the Italian Gastric Cancer Study Group prospective multicenter surgical study. Clin Oncol. 1998 Apr;16(4):1490–3. doi: 10.1200/JCO.1998.16.4.1490. [DOI] [PubMed] [Google Scholar]
  • 23.Degiuli M, Sasako M, Ponti A, Calvo F. Survival results of a multicentre phase II study to evaluate D2 gastrectomy for gastric cancer. Br J Cancer. 2004 May 4;90(9):1727–32. doi: 10.1038/sj.bjc.6601761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Song W, He Y, Wang S, He W, Xu J. Significance of the lymph nodes in the 7th station in rational dissection for metastasis of distal gastric cancer with different T categories. Chin J Cancer Res. 2014 Aug;26(4):423–30. doi: 10.3978/j.issn.1000-9604.2014.08.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Galizia G, Lieto E, De Vita F, Castellano P, Ferraraccio F, Zamboli A, Mabilia A, Auricchio A, De Sena G, De Stefano L, Cardella F, Barbarisi A, Orditura M. Modified versus standard D2 lymphadenectomy in total gastrectomy for nonjunctional gastric carcinoma with lymph nodes metastases. Srgery. 2015 Feb;157(2):285–96. doi: 10.1016/j.surg.2014.09.012. [DOI] [PubMed] [Google Scholar]
  • 26.Lee J, Lim do H, Kim S, et al. Phase III trial comparing capecitabine plus cisplatin versus capecitabine plus cisplatin with concurrent capecitabine radiotherapy in completely resected gastric cancer with D2 lymph node dissection: the ARTIST trial. J Clin Oncol. 2012;30:268–273. doi: 10.1200/JCO.2011.39.1953. [DOI] [PubMed] [Google Scholar]
  • 27.De Manzoni G, Verlato G, Roviello F, Morgagni P, Di Leo A, Saragoni L, Marrelli D, Kurihara H, Pasini F. The new TNM classification of lymph node metastasis minimises stage migration problems in gastric cancer patients. Br J Cancer. 2002 Jul 15;87(2):171–4. doi: 10.1038/sj.bjc.6600432. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Cuschieri A, Weeden S, Fielding J, Bancewicz J, Craven J, Joypaul V, Sydes M, Fayers P. Patient survival after D1 and D2 resections for gastric cancer: long-term results of the MRC randomized surgical trial. Surgical Co-operative Group. Br J Cancer. 1999;79(9-10):1522–30. doi: 10.1038/sj.bjc.6690243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Cuschieri A, Fayers P, Fielding J, Craven J, Bancewicz J, Joypaul V, Cook P. Postoperative morbidity and mortality after D1 and D2 resections for gastric cancer: preliminary results of the MRC randomised controlled surgical trial. Lancet. 1996 Apr 13;347(9007):995–9. doi: 10.1016/s0140-6736(96)90144-0. [DOI] [PubMed] [Google Scholar]
  • 30.McCulloch P, Nita ME, Kazi H, Gama-Rodrigues J. Extended versus limited lymph nodes dissection technique for adenocarcinoma of the stomach. Cochrane Database Syst Rev. 2004 Oct 18;4:CD001964. doi: 10.1002/14651858.CD001964.pub2. [DOI] [PubMed] [Google Scholar]
  • 31.Songun I, Putter H, Kranenbarg EM, Sasako M, van de Velde CJ. Surgical treatment of gastric cancer: 15-year follow-up results of the randomised nationwide Dutch D1D2 trial. Lancet Oncol. 2010;11:439–49. doi: 10.1016/S1470-2045(10)70070-X. [DOI] [PubMed] [Google Scholar]
  • 32.De Manzoni G, Verlato G, Bencivenga M, Marrelli D, Di Leo A, Giacopuzzi S, Cipollari C, Roviello F. Impact of super-extended lymphadenectomy on relapse in advanced gastric cancer. Eur J Surg Oncol. 2015 Apr;41(4):534–40. doi: 10.1016/j.ejso.2015.01.023. [DOI] [PubMed] [Google Scholar]
  • 33.Roviello F, Pedrazzani C, Marrelli D, Di Leo A, Caruso S, Giacopuzzi S, Corso G, de Manzoni G. Super-extended (D3) lymphadenectomy in advanced gastric cancer. Eur J Surg Oncol. 2010 May;36(5):439–46. doi: 10.1016/j.ejso.2010.03.008. [DOI] [PubMed] [Google Scholar]
  • 34.Sasako M, Sano T, Yamamoto S, Kurokawa Y, Nashimoto A, Kurita A, et al. D2 lymphadenectomy alone or with para-aortic nodal dissection for gastric cancer. N Engl J Med. 2008;359:453–62. doi: 10.1056/NEJMoa0707035. [DOI] [PubMed] [Google Scholar]
  • 35.Wu CW, Hsiung CA, Lo SS, et al. Nodal dissection for patients with gastric cancer: a randomised controlled trial. Lancet Oncol. 2006;7:309–15. doi: 10.1016/S1470-2045(06)70623-4. [DOI] [PubMed] [Google Scholar]
  • 36.Songun I, Putter H, Kranenbarg EM, Sasako M, van de Velde CJ. Surgical treatment of gastric cancer: 15-year follow-up results of the randomised nationwide Dutch D1D2 trial. Lancet Oncol. 2010;11:439–49. doi: 10.1016/S1470-2045(10)70070-X. [DOI] [PubMed] [Google Scholar]
  • 37.Schwarz RE, Karpeh MS, Brennan MF. Surgical management of gastric cancer: the Western experience. Management of upper gastrointestinal cancer. In: Daly JM, Hennessy TPJ, Reynolds JV, editors. London: W.B. Saunders; 1999. pp. 83–106. [Google Scholar]
  • 38.Kodera Y, Schwarz RE, Nakao A. Extended lymph node dissection in gastric carcinoma: where do we stand after the Dutch and British randomized trials? J Am Coll Surg. 2002;195:855–64. doi: 10.1016/s1072-7515(02)01496-5. [DOI] [PubMed] [Google Scholar]
  • 39.Kuo CY, Chao Y, Li CP. Update on treatment of gastric cancer. J Chin Med Assoc. 2014 Jul;77(7):345–53. doi: 10.1016/j.jcma.2014.04.006. [DOI] [PubMed] [Google Scholar]
  • 40.Schwarz RE. Spleen-preserving splenic hilar lymphadenectomy at the time of gastrectomy for cancer: Technical feasibility and early results. J Surg Oncol. 2002;79:73–6. doi: 10.1002/jso.10036. [DOI] [PubMed] [Google Scholar]
  • 41.Wu CW, Hsiung CA, Lo SS, Hsieh MC, Shia LT, Whang-Peng J. Randomized clinical trial of morbidity after D1 and D3 surgery for gastric cancer. Br J Surg. 2004 Mar;91(3):283–7. doi: 10.1002/bjs.4433. [DOI] [PubMed] [Google Scholar]
  • 42.Wu CW, Hsiung CA, Lo SS, Hsieh MC, Chen JH, Li AF, Lui WY, Whang-Peng J. Nodal dissection for patients with gastric cancer: a randomised controlled trial. Lancet Oncol. 2006 Apr;7(4):309–15. doi: 10.1016/S1470-2045(06)70623-4. [DOI] [PubMed] [Google Scholar]
  • 43.Sano T, Sasako M, Yamamoto S, Nashimoto A, Kurita A, Hiratsuka M, Tsujinaka T, Kinoshita T, Arai K, Yamamura Y, Okajima K. Gastric cancer surgery: morbidity and mortality results from a prospective randomized controlled trial comparing D2 and extended paraortic lymphadenectomy-Japan Clinical Oncology group Study 9501. J Clinical Oncol. 2004 Jul 15;22(14):2767–73. doi: 10.1200/JCO.2004.10.184. [DOI] [PubMed] [Google Scholar]
  • 44.Coccolini F, Cotte E, Glehen O, Lotti M, Poiasina E, Catena F, Yonemura Y, Ansaloni L. Intraperitoneal chemotherapy in advanced gastric cancer. Meta-analysis of randomized trials. Eur J Surg Oncol. 2014 Jan;40(1):12–26. doi: 10.1016/j.ejso.2013.10.019. [DOI] [PubMed] [Google Scholar]
  • 45.Yonemura Y, Elnemr A, Endou Y, et al. Multidisciplinary therapy for treatment of patients with peritoneal carcinomatosis from gastric cancer. World J Gastrointetinal Oncol. 2010;2:85–97. doi: 10.4251/wjgo.v2.i2.85. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Montori G, Coccolini F, Ceresoli M, Catena F, Colaianni N, Poletti E, Ansaloni L. The treatment of peritoneal carcinomatosis in advanced gastric cancer: state of the art. Int J Surg Oncol. 2014;2014:912418. doi: 10.1155/2014/912418. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Rudloff U, Langan RC, Mullinax JE, et al. Impact of maximal cytoreductive surgery plus regional heated intraperitoneal chemotherapy (HIPEC) on outcome of patients with peritoneal carcinomatosis of gastric origin: results of the GYMSSA trial. J Surg Oncol. 2014 Sep;110(3):275–84. doi: 10.1002/jso.23633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Fugazzola P, Coccolini F, Montori G, Ceresoli M, Baggi P, Costanzo A, Tomasoni M, Gregis F, Nozza S, Ansaloni L. Overall and disease-free survival in patients treated with CRS + HIPEC with cisplatin and paclitaxel for gastric cancer with peritoneal carcinomatosis. J Gastrointest Oncol. 2017 Jun;8(3):572–582. doi: 10.21037/jgo.2017.03.11. doi: 10.21037/jgo.2017.03.11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Coccolini F, Gheza F, Lotti M, Virzì S, Iusco D, Ghermandi C, Melotti R, Baiocchi G, Giulini SM, Ansaloni L, Catena F. Peritoneal carcinomatosis. World J Gastroenterol. 2013 Nov 7;19(41):6979, 94. doi: 10.3748/wjg.v19.i41.6979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Bristow RE, Chi DS. Platinum-based neoadjuvant chemotherapy and interval surgical cytoreduction for advanced ovarian cancer: a meta-analysis. Gynecol Oncol. 2006 Dec;103(3):1070–6. doi: 10.1016/j.ygyno.2006.06.025. Epub 2006 Jul 27. [DOI] [PubMed] [Google Scholar]
  • 51.Coccolini F, Campanati L, Catena F, Ceni V, Ceresoli M, Jimenez Cruz J, Lotti M, Magnone S, Napoli J, Rossetti D, De Iaco P, Frigerio L, Pinna A, Runnebaum I, Ansaloni L. Hyperthermic intraperitoneal chemotherapy with cisplatin and paclitaxel in advanced ovarian cancer: a multicenter prospective observational study. J Gynecol Oncol. 2015 Jan;26(1):54–61. doi: 10.3802/jgo.2015.26.1.54. doi: 10.3802/jgo.2015.26.1.54. Epub 2014 Nov 3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Yonemura Y, Shinbo M, Hagiwara A, et al. Treatment for potentially curable gastric cancer patients with intraperitoneal free cancer cells. Gastroenterological Surg. 2008;31:802–12. [in Japanese] [Google Scholar]
  • 53.Yonemura Y, Bandou E, Sawa T, et al. Neoadjuvant treatment of gastric cancer with peritoneal dissemination. EJSO. 2006;32:661–5. doi: 10.1016/j.ejso.2006.03.007. [DOI] [PubMed] [Google Scholar]
  • 54.Glehen O, Gilly FN, Arvieux C, Cotte E, Boutitie F, Mansvelt B, Bereder JM, Lorimier G, Quenet F, Elias D, Chirurgie Association Française de. Peritoneal carcinomatosis from gastric cancer: a multi-institutional study of 159 patients treated by cytoreductive surgery combined with perioperative intraperitoneal chemotherapy. Ann Surg Oncol. 2010 Sep;17(9):2370–7. doi: 10.1245/s10434-010-1039-7. doi: 10.1245/s10434-010-1039-7. Epub 2010 Mar 25. [DOI] [PubMed] [Google Scholar]
  • 55.Yonemura Y, Endou Y, Shinbo M, et al. Safety and efficacy of bidirectional chemotherapy for treatment of patients with peritoneal dissemination from gastric cancer: selection for cytoreductive surgery. J Surg Oncol. 2009;100:311–6. doi: 10.1002/jso.21324. [DOI] [PubMed] [Google Scholar]
  • 56.Yonemura Y, Kawamura T, Bandou E, et al. Treatment of peritoneal dissemination from gastric cancer by peritonectomy and chemohyperthermic peritoneal perfusion. Brit J Surg. 2005;92:370–5. doi: 10.1002/bjs.4695. [DOI] [PubMed] [Google Scholar]
  • 57.Glehen O, Gilly FN, Boutitie F, Bereder JM, Quenet F, Sideris L, Mansvelt B, Lorimier G, Msika S. Elias D and Association., French Surgical. Toward curative treatment of peritoneal carcinomatosis from nonovarian origin by cytoreductive surgery combined with perioperative intraperitoneal chemotherapy: a multi-institutional study of 1,290 patients. Cancer. 2010 Dec 15;116(24):5608–18. doi: 10.1002/cncr.25356. doi: 10.1002/cncr.25356. Epub 2010 Aug 24. [DOI] [PubMed] [Google Scholar]
  • 58.Coccolini F, Catena F, Glehen O, Yonemura Y, Sugarbaker PH, Piso P, Montori G, Ansaloni L. Complete versus incomplete cytoreduction in peritoneal carcinosis from gastric cancer, with consideration to PCI cut-off. Systematic review and meta-analysis. Eur J Surg Oncol. 2015 april 14 doi: 10.1016/j.ejso.2015.03.231. [DOI] [PubMed] [Google Scholar]
  • 59.Scaringi S, Kianmanesh R, Sabate JM, Facchiano E, Jouet P, Coffin B, Parmentier G, Hay JM, Flamant Y, Msika S. Advanced gastric cancer with or without peritoneal carcinomatosis treated with hyperthermic intraperitoneal chemotherapy: a single western center experience. Eur J Surg Oncol. 2008 Nov;34(11):1246–52. doi: 10.1016/j.ejso.2007.12.003. doi: 10.1016/j.ejso.2007.12.003. Epub 2008 Jan 28. [DOI] [PubMed] [Google Scholar]
  • 60.Yang XJ, Li Y, Yonemura Y. Cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy to treat gastric cancer with ascites and/or peritoneal carcinomatosis: Results from a Chinese center. J Surg Oncol. 2010 May 1;101(6):457–64. doi: 10.1002/jso.21519. [DOI] [PubMed] [Google Scholar]
  • 61.Yang XJ, Huang CQ, Suo T, Mei LJ, Yang GL, Cheng FL, Zhou YF, Xiong B, Yonemura Y, Li Y. Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy improves survival of patients with peritoneal carcinomatosis from gastric cancer: final results of a phase III randomized clinical trial. Ann Surg Oncol. 2011 Jun;18(6):1575–81. doi: 10.1245/s10434-011-1631-5. doi: 10.1245/s10434-011-1631-5. Epub 2011 Mar 23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Yamaguchi K, Yoshida K, Tanahashi T, Takahashi T, Matsuhashi N, Tanaka Y, Tanabe K, Ohdan H. The long-term survival of stage IV gastric cancer patients with conversion therapy. Gastric Cancer. 2018;21:315–323. doi: 10.1007/s10120-017-0738-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Fujitani Kazumasa, Yang Han-Kwang, Mizusawa Junki, Kim Young-Woo, Terashima Masanori, et al. Gastrectomy plus chemotherapy versus chemotherapy alone for advanced gastric cancer with a single non-curable factor (REGATTA): a phase 3, randomised controlled trial. Lancet Oncol. 2016;17:309–18. doi: 10.1016/S1470-2045(15)00553-7. [DOI] [PubMed] [Google Scholar]
  • 64.Yoshida K, Yamaguchi K, Okumura N, Tanahashi T, Kodera Y. Is conversion theraphy possible in stage IV gastriccancer: the proposal of new biological categories of classification. Gastric Cancer. 2016;19:329–338. doi: 10.1007/s10120-015-0575-z. DOI 10.1007/s10120-015-0575-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Ministrini S, Solaini L, Cipollari C, Sofia S, Marino E, D’Ignazio A, Bencivenga M, Tiberio GAM. Surgical treatment of hepatic metastases from gastric cancer. Updates in Surgery. 2018;70:273–278. doi: 10.1007/s13304-018-0536-2. https://doi.org/10.1007/s13304-018-0536-2 . [DOI] [PubMed] [Google Scholar]
  • 66.Kitano S, Shiraishi N, Fujii K, Yasuda K, Inomata M, Adachi Y. A randomized controlled trial comparing open vs laparoscopy-assisted distal gastrectomy for the treatment of early gastric cancer: an interim report. Surgery. 2002;131:S306–S311. doi: 10.1067/msy.2002.120115. [DOI] [PubMed] [Google Scholar]
  • 67.Lee JH, Han HS, Lee JH. A prospective randomized study comparing open vs laparoscopy-assisted distal gastrectomy in early gastric cancer: early results. Surg Endosc. 2005;19:168–173. doi: 10.1007/s00464-004-8808-y. [DOI] [PubMed] [Google Scholar]
  • 68.Kim HH, Hyung WJ, Cho GS, Kim MC, Han SU, Kim W, Ryu SW, Lee HJ, Song KY. Morbidity and mortality of laparoscopic gastrectomy versus open gastrectomy for gastric cancer: an interim report--a phase III multicenter, prospective, randomized Trial (KLASS Trial) Ann Surg. 2010 Mar;251(3):417–20. doi: 10.1097/SLA.0b013e3181cc8f6b. doi: 10.1097/SLA.0b013e3181cc8f6b. [DOI] [PubMed] [Google Scholar]
  • 69.Yasunaga H, Horiguchi H, Kuwabara K, Matsuda S, Fushimi K, Hashimoto H, Ayanian JZ. Outcomes after laparoscopic or open distal gastrectomy for early-stage gastric cancer: a propensity-matched analysis. Ann Surg. 2013;257:640–646. doi: 10.1097/SLA.0b013e31826fd541. [DOI] [PubMed] [Google Scholar]
  • 70.Bonenkamp JJ, Songun I, Hermans J, Sasako M, Welvaart K, Plukker JT, van Elk P, Obertop H, Gouma DJ, Taat CW. Randomised comparison of morbidity after D1 and D2 dissection for gastric cancer in 996 Dutch patients. Lancet. 1995;345:745–748. doi: 10.1016/s0140-6736(95)90637-1. [DOI] [PubMed] [Google Scholar]
  • 71.Wang W, Zhang X, Shen C, Zhi X, Wang B, et al. Laparoscopic versus Open Total Gastrectomy for Gastric Cancer: An Updated Meta-Analysis. PLoS ONE. 2014;9(2):e88753. doi: 10.1371/journal.pone.0088753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Xiong JJ, Nunes QM, Huang W, Tan CL, Ke NW, Xie SM, Ran X, Zhang H, Chen YH, Liu XB. Laparoscopic vs open total gastrectomy for gastric cancer: A meta-analysis. World J Gastroenterol. 2013;19(44):8114–8132. doi: 10.3748/wjg.v19.i44.8114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Liao G, Chen J, Ren C, Li R, Du S, Xie G, Deng H, Yang K, Yuan Y. Robotic versus Open Gastrectomy for Gastric Cancer: A Meta-Analysis. PLoS ONE. 2013;8(12):e81946. doi: 10.1371/journal.pone.0081946. [DOI] [PMC free article] [PubMed] [Google Scholar]

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