| Literature DB >> 29740588 |
Gerassimos N Douridas1, Stefanos K Pierrakakis1.
Abstract
Although D2 constitutes the level of lymph node dissection which most surgical associations endorse in their treatment guidelines for gastric cancer more extended D3 dissection has also been attempted to improve oncologic outcomes. Existing literature pertinent with the provisional therapeutic impact of D3 lymphadenectomy in advanced gastric cancer is studied in this mini review. Seven non-randomized comparisons, three randomized trials and five meta-analyses, almost exclusively of Asian origin, were identified and examined. D3 compared to D2 lymphadenectomy consistently and significantly proved to be associated with a "heavier" iatrogenic surgical trauma translated to more blood loss, prolonged operative time, higher relaparotomy rates and post-procedural surgical and non-surgical morbidity. Oddly mortality in most of these series did not reach statistical significance a fact probably attributed to Asian surgical expertise and/or methodologic drawbacks. All existing evidence and their meta-analyses, including a well-designed RCT from Japan (JCOG), failed to support a clear overall survival benefit linked to D3 dissection thus excluding the procedure from current treatment algorithms. The Italian GC research group, analyzing their database, proposed tumor histology, macroscopic type, size and location as selection criteria for D3 dissection provided surgical expertise is available. Recently, a phase II clinical trial from Japan reported a 3 -year survival rate of 59% in patients with clinically involved para-aortic nodes treated with neoadjuvant chemotherapy followed by D3 lymphadenectomy, rekindled the issue. Future multicenter randomized trials should test the extend and after effect of lymphadenectomy in gastric cancer combined with modern chemotherapeutic agents in multimodal treatments.Entities:
Keywords: D3; cancer; extend; gastrectomy; gastric; lymph nodes; lymphadenectomy; surgery
Year: 2018 PMID: 29740588 PMCID: PMC5931173 DOI: 10.3389/fsurg.2018.00027
Source DB: PubMed Journal: Front Surg ISSN: 2296-875X
Figure 1Micro-metastatic involvement of para-aortic nodes is considered borderline resectable disease, (gray ellipse), and could either be eliminated by surgery (D3 dissection) or sterilized with neoadjuvant chemotherapy and then resected by surgery. Macrometastatic involvement of distant nodes (stations 13–16) is classified as M overriding surgery’s endogenous therapeutic potential.
Details and outcomes of studies included in the mini review.
| Tokunaga M, 2010, Japan ( | Retrospective cohort, Single center ( | “curative resection” PALN dissection | Morb:30%, Mort: 2%, 5yOS:13%Macroscopic type and number of positive nodes independent risk factors | |
| Maeta M, 1999, Japan ( | Prospective, pilot not randomized, single center ( | T3–T4 tumors, normal nodes in CTD3 vs D4 | D3 morb:26% D4 morb:40% SSFU ≤ 30 monthsOS NS | |
| Bostanci E, 2004, Turkey ( | Retrospective cohort, not randomized, single center ( | D2 vs D3 | D2 Morb: 10% D3 Morb: 35% Morbidity SSD2 Mort: 1% D3 Mort :8% Mortality SS | |
| Kunisaki C, 2006, Japan ( | Retrospective comparison, not randomized, multicenter ( | T4 tumors (beyond sub-serosa)D2 vs D3 | Morbidity NS (except bleeding, pulmonary and renal complications)Mortality NS | |
| Hu J, 2009, China ( | Retrospective comparison, not randomized, single center ( | D2 vs D2 + PALN | D2 Morb:24,2% D2 + Morb:27,3% Morbidity NS D2 mort: 0% D2 + mort 1,8% Mortality NS Survival (5y): 65,8% vs 66,1% NS | |
| De Manjoni G, 2011 and 2015, Italy ( | GIRGC retrospective database analysis, observational, multicenter ( | D2 vs D3 | – | |
| Tsuburaya A, 2014, Japan ( | JCOG observational, multicenter ( | “bulky” pN2 and or PAN + in imagingS1 + cisplatin (4 weeks) followed by D2 + PALN | OS (3y): 59% OS (5y): 53%Grade3/4 toxicity: 34.4% | |
| Kulig J, 2007, Poland ( | PGCSG, pilot, RCT, multicenter, ( | D2 vs D2 + PALN | Interim safety analysisMorbidity: 27,7 vs 21,6% NSMortality: 4,9 vs 2,2% NS | |
| Sasako M, 2008, Japan ( | JCOG, multicenter, RCT ( | T2b, T3, T4 and “not obvious + PALN nodes”D2 vs D2 + PALN | OS (5y): 69,2 vs 70,3% NSDFS (5y): 62,6 vs 61,7% NS | |
| Yonemura Y, 2008, Japan, Taiwan, Korea ( | EASOG, multicenter, multinational RCT ( | Pts with enlarged PALN at CT excludedD2 vs D3 | Mortality: 0,74 vs 3,73% NSOS (5y): 52,6% vs 55% NS | |
| Wang Z, 2010, China ( | Meta-analysis 4RCT, 4nonRCT trials ( | D2 vs D2 + PALN | OS (5y): RR 0.96 vs 1.04 NS Mortality: RR 0.99 vs 2.06 NS | |
| Lustosa S, 2008, Brazil ( | Meta-analysis 5RCT D1vsD2vsD3 of which 2RCT D1vsD3 ( | D1 vs D3 | Morbidity RR 2.35 vs 4.07 SS OS 5(y): RR 0,83 vs 1,38 NS | |
| Yang S, 2009, China ( | Meta-analysis 5RCT ( | D2 vs D3 | Morbidity: 24,7 vs 29,6% NS Mortality: 2,3 vs 2,2% NS | |
| Chen X, 2010, China ( | Meta-analysis 3RCT ( | D2 vs D2 + PALD | Morbidity | |
| Mocellin S, 2015, Italy ( | Meta-analysis 3RCT ( | D2 vs D3 | OS 5(y) |
Concluding remarks of each study are typed in bold text and listed in the outer-right column.
pts, patients; morb, morbidity; mort, mortality; DFS, disease free survival; DSS, disease specific survival; GIRGC, Group of Italian Research in Gastric Cancer; JCOG, Japanese Clinical Oncology Group; PGCSG, Polish Gastric Cancer Study Group; PALN/D, para-aortic lymph nodes/dissection; OS, overall survival; NS, non-significant; SS, statistically significant; RR, risk ratio.