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review of literature on clinical pancreatology - The Pancreapedia

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understand the utility <str<strong>on</strong>g>of</str<strong>on</strong>g> these devices, <strong>on</strong>e need to first c<strong>on</strong>sider mechanical properties suchas radial force (expansi<strong>on</strong> force) and axial force (straightening force) [517].Endoscopic biliary drainage is widely accepted as palliative treatment in patients withpancreatic cancer. One study was designed to compare self-expanding metal stent andpolyethylene stent in a homogeneous patient group with advanced pancreatic cancer. <strong>The</strong>study included 154 patients initially treated with a metal or plastic stent. Median survival time,stent patency, and stent-associated hospital admissi<strong>on</strong>s were evaluated. <strong>The</strong> mediansurvival time in patients treated with metal and plastic stent was 6 and 4 m<strong>on</strong>ths,respectively. Self-expanding metal stents have a significantly higher patency rate thanpolyethylene stents. Stent occlusi<strong>on</strong> was observed in 21 (33 %) <str<strong>on</strong>g>of</str<strong>on</strong>g> 63 patients in the plasticstent group after a median period <str<strong>on</strong>g>of</str<strong>on</strong>g> 57 days and in 17 (19 %) <str<strong>on</strong>g>of</str<strong>on</strong>g> 91 patients in the metalstent group after a median period <str<strong>on</strong>g>of</str<strong>on</strong>g> 126 days. <strong>The</strong> total time <str<strong>on</strong>g>of</str<strong>on</strong>g> hospital stay after initialimplantati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> metal or plastic stent was 7 and 17 days, respectively. It was c<strong>on</strong>cluded thatself-expanding metal stents have a l<strong>on</strong>ger patency than polyethylene stents. Additi<strong>on</strong>ally, thenumber <str<strong>on</strong>g>of</str<strong>on</strong>g> stent-associated hospital admissi<strong>on</strong>s and the total time <str<strong>on</strong>g>of</str<strong>on</strong>g> hospital stay werehigher in the plastic stent group. <strong>The</strong> median survival time was not significantly different inboth groups [518].Predicti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> survival<strong>The</strong> pancreatic nomogram, originally developed in the Memorial Sloan-Kettering CancerCenter in the USA, combines clinicopathological and operative data to predict diseasespecificsurvival at 1, 2 and 3 years from initial resecti<strong>on</strong>. An external patient cohort from aretrospective pancreatic adenocarcinoma database at the Academic Medical Centre inAmsterdam was used to test the validity <str<strong>on</strong>g>of</str<strong>on</strong>g> the pancreatic adenocarcinoma nomogram. <strong>The</strong>cohort included 263 c<strong>on</strong>secutive patients who had surgery between 1985 and 2004. Data forall the necessary variables were available for 256 patients (97 %). At the last follow-up, 35patients were alive, with a median follow-up <str<strong>on</strong>g>of</str<strong>on</strong>g> 27 (range 3-114) m<strong>on</strong>ths. <strong>The</strong> 1-, 2- and 3-year disease-specific survival rates were 61, 30 and 16 percent respectively. <strong>The</strong> nomogramc<strong>on</strong>cordance index was 0.61. <strong>The</strong> calibrati<strong>on</strong> analysis <str<strong>on</strong>g>of</str<strong>on</strong>g> the model showed that the predictedsurvival did not significantly deviate from the actual survival. <strong>The</strong> Memorial Sloan-KetteringCancer Center pancreatic cancer nomogram provided an accurate survival predicti<strong>on</strong>. It mayaid in counselling patients and in stratificati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> patients for <strong>clinical</strong> trials [519].Identificati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> defined patient groups based <strong>on</strong> a prognostic index may improve thepredicti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> survival and selecti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> therapy for patients with pancreatic cancer. Manyprognostic factors have been identified <str<strong>on</strong>g>of</str<strong>on</strong>g>ten based <strong>on</strong> retrospective, underpowered studieswith unclear analyses. Data from 653 patients were analysed. C<strong>on</strong>tinuous variables are <str<strong>on</strong>g>of</str<strong>on</strong>g>tensimplified assuming a linear relati<strong>on</strong>ship with log hazard or introducing a step functi<strong>on</strong>(dichotomising). Misspecificati<strong>on</strong> may lead to inappropriate c<strong>on</strong>clusi<strong>on</strong>s but has not beenpreviously investigated in pancreatic cancer studies. Models based <strong>on</strong> standard assumpti<strong>on</strong>swere compared with a novel approach using n<strong>on</strong>linear fracti<strong>on</strong>al polynomial transformati<strong>on</strong>s.<strong>The</strong> model based <strong>on</strong> fracti<strong>on</strong>al polynomial-transformed covariates was most appropriate andc<strong>on</strong>firmed five previously reported prognostic factors: albumin, CA 19-9, alkalinephosphatase, LDH and metastases, and identified three additi<strong>on</strong>al factors not previouslyreported: WBC, AST and BUN. <strong>The</strong> effects <str<strong>on</strong>g>of</str<strong>on</strong>g> CA 19-9, alkaline phosphatase, AST and BUNmay go unrecognised due to simplistic assumpti<strong>on</strong>s made in statistical modelling. Weadvocate a multivariable approach that uses informati<strong>on</strong> c<strong>on</strong>tained within c<strong>on</strong>tinuousvariables appropriately. <strong>The</strong> functi<strong>on</strong>al form <str<strong>on</strong>g>of</str<strong>on</strong>g> the relati<strong>on</strong>ship between c<strong>on</strong>tinuouscovariates and survival should always be assessed [520].

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