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review of literature on clinical pancreatology - The Pancreapedia

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was observed in the NACRT group. <strong>The</strong> frequency <str<strong>on</strong>g>of</str<strong>on</strong>g> residual tumor grading in the NACRTgroup was significantly different from that in surgery-al<strong>on</strong>e (R0/1/2 %, 52/15/33 vs 22/51/27).In R0/1 cases, overall survival and disease-free survival rates in the NACRT group (n=18)were significantly l<strong>on</strong>ger than in surgery-al<strong>on</strong>e (n=30). <strong>The</strong> rate <str<strong>on</strong>g>of</str<strong>on</strong>g> local recurrence in theNACRT group was significantly less than in surgery-al<strong>on</strong>e (11 % vs 47 %). It was c<strong>on</strong>cludedthat this single-instituti<strong>on</strong> experience indicates that neoadjuvant chemoradiati<strong>on</strong> therapy isable to increase the resectability rate with clear margins and to decrease the rate <str<strong>on</strong>g>of</str<strong>on</strong>g>metastatic lymph nodes, resulting in improved prognosis <str<strong>on</strong>g>of</str<strong>on</strong>g> curative cases with pancreaticcancer that extended bey<strong>on</strong>d the pancreas [526].Adjuvant chemoradiati<strong>on</strong><strong>The</strong> role <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant chemoradiati<strong>on</strong> therapy (CRT) in pancreatic cancer remainsc<strong>on</strong>troversial. <strong>The</strong> primary aim <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>on</strong>e study was therefore to determine if CRT improvedsurvival in patients with resected pancreatic cancer in a large, multiinstituti<strong>on</strong>al cohort <str<strong>on</strong>g>of</str<strong>on</strong>g>patients. Patients undergoing resecti<strong>on</strong> for pancreatic adenocarcinoma from seven academicmedical instituti<strong>on</strong>s were included. Exclusi<strong>on</strong> criteria included patients with T4 or M1 disease,R2 resecti<strong>on</strong> margin, preoperative therapy, chemotherapy al<strong>on</strong>e, or if adjuvant therapy statuswas unknown. <strong>The</strong>re were 747 patients included in the initial evaluati<strong>on</strong>. Primary analysiswas performed between patients that had surgery al<strong>on</strong>e (n=374) and those receivingadjuvant CRT (n=299). Median follow-up time was 12 m<strong>on</strong>ths and 15 m<strong>on</strong>ths, respectively,for survivors. Median overall survival for patients receiving adjuvant CRT was significantlyl<strong>on</strong>ger than for those undergoing operati<strong>on</strong> al<strong>on</strong>e (20 vs 15 m<strong>on</strong>ths). On subset andmultivariate analysis, adjuvant CRT dem<strong>on</strong>strated a significant survival advantage <strong>on</strong>lyam<strong>on</strong>g patients who had lymph node (LN)-positive disease (hazard ratio 0.48, 95 % CI 0.36to 0.64) and not for LN-negative patients (hazard ratio 0.81, 95 % CI 0.56 to 1.18). Diseasefreesurvival in patients with LN-negative disease who received adjuvant CRT wassignificantly worse than in patients who had surgery al<strong>on</strong>e (15 m<strong>on</strong>ths vs 19 m<strong>on</strong>ths). Thusthis large multiinstituti<strong>on</strong>al study emphasizes the importance <str<strong>on</strong>g>of</str<strong>on</strong>g> analyzing subsets <str<strong>on</strong>g>of</str<strong>on</strong>g> patientswith pancreas adenocarcinoma who have LN metastasis. Benefit <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant CRT is seen<strong>on</strong>ly in patients with LN-positive disease, regardless <str<strong>on</strong>g>of</str<strong>on</strong>g> resecti<strong>on</strong> margin status. CRT inpatients with LN-negative disease may c<strong>on</strong>tribute to reduced disease-free survival [527].Pre- plus postoperative chemoradiati<strong>on</strong>To evaluate both the feasibility and efficacy <str<strong>on</strong>g>of</str<strong>on</strong>g> our combined therapy, which c<strong>on</strong>sisted <str<strong>on</strong>g>of</str<strong>on</strong>g>preoperative chemoradiati<strong>on</strong>, surgery, and postoperative liver perfusi<strong>on</strong> chemotherapy (LPC)for patients with T3 (extended bey<strong>on</strong>d the pancreatic c<strong>on</strong>fines) cancer <str<strong>on</strong>g>of</str<strong>on</strong>g> the pankreas 38patients with T3-pancreatic cancers c<strong>on</strong>sented to receive a combinati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> preoperativechemoradiati<strong>on</strong>, surgery, and postoperative LPC 2002 to 2007. With the aid <str<strong>on</strong>g>of</str<strong>on</strong>g> 3D radiati<strong>on</strong>planning, irradiati<strong>on</strong> fields were c<strong>on</strong>structed that included both the primary pancreatic tumorand retropancreatic tissues while taking care to exclude any secti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> the gastrointestinaltract. <strong>The</strong> total dose <str<strong>on</strong>g>of</str<strong>on</strong>g> radiati<strong>on</strong> was 50 Gy (2 Gy x 25 fracti<strong>on</strong>s/5 weeks) and wasadministered in combinati<strong>on</strong> with gemcitabine treatments (1000 mg/m/week x 9/3 m<strong>on</strong>ths).Preoperative restaging via computerized tomography and intraoperative inspecti<strong>on</strong> wereused to determine if pancreatectomy was indicated. For resected cases, <strong>on</strong>e catheter wasplaced into the gastroduodenal artery and another <strong>on</strong>e into the superior mesenteric vein.Postoperatively, 5-FU (125 mg/day x 28 days) was infused via each <str<strong>on</strong>g>of</str<strong>on</strong>g> these 2 routes.Preoperative chemoradiati<strong>on</strong> was completed for all 38 patients, including 3 patients whorequired gemcitabine-dose reducti<strong>on</strong>. Seven patients (18 %) did not undergo surgicalresecti<strong>on</strong> because either distant metastases or progressive local tumors had been detectedafter chemoradiati<strong>on</strong>. <strong>The</strong> remaining 31 patients (82 %) underwent pancreatectomy pluspostoperative perfusi<strong>on</strong> chemotherapy, without postoperative or in-hospital mortality. <strong>The</strong> 5-year survival rate after pancreatectomy was 53 percent, with low incidences <str<strong>on</strong>g>of</str<strong>on</strong>g> both localrecurrence (9 %) and liver metastasis (7 %). Postoperative histopathologic study revealed amarked degenerative change in cancer tissue, showing negative surgical margins (R0) for 30patients (96 %) and negative nodal involvement for 28 patients (90 %) [528].

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