Impact of lymph node ratio on survival in patients with pancreatic and periampullary cancer. Issue 3 (22nd December 2014)

• Record Type: Journal Article
• Authors: Tol, J. A. M. G.; Brosens, L. A. A.; van Dieren, S.; van Gulik, T. M.; Busch, O. R. C.; Besselink, M. G. H.; Gouma, D. J.
• Is Part Of: British journal of surgery. Volume 102:Issue 3(2015:Mar.)
• Page Start: 237
• Page End: 245
• Publication Date: 2014-12-22
• Subjects: Surgery -- Periodicals; 617.005
• DOI: 10.1002/bjs.9709
• Languages: English
• ISSNs: 0007-1323

Abstract

<abstract abstract-type="main" id="bjs9709-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bjs9709-sec-0001" sec-type="section"> <title>Background</title> <p id="bjs9709-para-0001">According to some studies, the number of lymph nodes with metastases in relation to the total number of removed lymph nodes, the lymph node ratio (LNR), is one of the most powerful predictors of survival after resection in patients with pancreatic cancer. However, contradictory results have been reported, and small sample sizes of the cohorts and different definitions of a microscopic positive resection margin (R1) hamper the interpretation of data.</p> </sec> <sec id="bjs9709-sec-0002" sec-type="section"> <title>Methods</title> <p id="bjs9709-para-0002">The predictive value of LNR for 3‐year survival was assessed using a Cox proportional hazards model. From 1992 to 2012, all patients with pancreatic and periampullary cancer operated on with pancreatoduodenectomy were selected from a database. Clinicopathological characteristics were analysed. Microscopic positive resection margin was defined as the microscopic presence of tumour cells within 1 mm of the margins. A nomogram was created.</p> </sec> <sec id="bjs9709-sec-0003" sec-type="section"> <title>Results</title> <p id="bjs9709-para-0003">Some 760 patients were included. Predictive factors for death in 350 patients with pancreatic ductal adenocarcinoma included in the nomogram were: R1 resection (hazard ratio (HR) 1·55, 95 per cent c.i. 1·07 to 2·25), poor tumour differentiation (HR 2·78, 1·40 to 5·52), LNR above 0·18 (HR 1·75, 1·13 to 2·70) and no adjuvant therapy (HR 1·54, 1·01 to 2·34). The <italic>C</italic> statistic was 0·658 (0·632 to 0·698), and calibration was good (Hosmer–Lemeshow χ<sup>2</sup> = 5·67, <italic>P</italic> =0·773). LNR and poor tumour differentiation (HR 4·51 and 3·30 respectively) were also predictive in patients with distal common bile duct (CBD) cancer. LNR, R1 resection and jaundice were predictors of death in patients with ampullary cancer (HR 7·82, 2·68 and 1·93 respectively).</p> </sec> <sec id="bjs9709-sec-0004" sec-type="section"> <title>Conclusion</title> <p id="bjs9709-para-0004">LNR is a common predictor of poor survival in pancreatic, distal CBD and ampullary cancer.</p> </sec> </abstract>