PANCREATECTOMY WITH MESENTERIC AND PORTAL VEIN RESECTION FOR BORDERLINE RESECTABLE PANCREATIC CANCER: MULTICENTER STUDY

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PROPOSAL: PANCREATECTOMY WITH MESENTERIC AND PORTAL VEIN RESECTION FOR BORDERLINE RESECTABLE PANCREATIC CANCER: MULTICENTER STUDY Pancreatic carcinoma represents the fourth-leading cause of cancer-related death in the United States with 46,420 estimated new cases for 2014 and 35,590 deaths. 1 In Europe, 103,773 new cases are estimated in 2012, 2 and 8.15 deaths/100,000 in men and 5.62/100,000 in women are predicted for 2015. 3 Surgical resection represents the only potentially curative treatment for pancreatic adenocarcinoma: 5-year survival for patients undergoing complete surgical resection approaches 25 %. 4 Unfortunately, approximately 80 % of patients are inoperable for locally advanced or metastatic disease. 5 Superior mesenteric vein (SMV) and portal vein (PV) invasion is frequent because of the proximity of these vessels to the uncinate process and pancreatic head. Potentially curative surgery is possible in these patients combining pancreatic resection with en bloc resection of the PV-SMV venous axis. 6 Single- center reports, systematic reviews, and metaanalyses have shown the feasibility and the advantages of this approach, which may provide survival results comparable to those obtained with standard pancreatectomy without venous resection. 7 10 Other studies have stressed the role of histological venous invasion as prognostic factor, reporting worst survival in patients with venous invasion confirmed by pathological examination. 11,12 A recent study has even questioned the utility of aggressive surgery in these cases. 13 The objective of this study, we previously published, is to update a multicentric study on a series of 406 patients with borderline resectable pancreatic cancer submitted to pancreatectomy with en bloc venous resection. 14 Our purpose is to analyze perioperative and survival results of this technique and to identify predictive factors of histological venous invasion. We also define the prognostic role of histological venous invasion and identify other prognostic factors of overall survival. PATIENTS AND METHODS The study will be an analysis of a multicenter database of patients submitted to pancreatectomy with en bloc SMV and/or PV resection for pancreatic adenocarcinoma. Consecutive patients treated in different centers will be recruted. Only patients with borderline resectable pancreatic cancer will be included in this study. Borderline pancreatic cancer will be defined according to

NCCN guidelines, version 2.2015. Collected data will include: patients characteristics, preoperative workup, tumor characteristics, surgical treatment, postoperative outcomes, histological tumor features, postoperative adjuvant therapies, and survival. Preoperative Workup and Treatment Diagnosis of pancreatic adenocarcinoma will be made by imaging and confirmed by pathological examination. Only patients with confirmed pathological diagnosis of pancreatic adenocarcinoma will be included. Preoperative workup will include contrast-enhanced thoracoabdominal computed tomography (CT); abdominal contrast-enhanced magnetic resonance (MR) will be performed in selected patients according to results of CT scan or in case of contraindication of CT scan. Echo-endoscopy with fine-needle aspiration will be performed in selected cases. Positron emission tomography (PET) will be used used only in highly selected cases. Indication and protocols of neoadjuvant treatment will be established case by case by the multidisciplinary tumor board of each single center, according to patients and tumors characteristics and to the expected probability to obtain an R0 resection. Surgery An Excell database, including all the necessary variables, will be emailed to the partecipating centers. Patients will undergo pancreaticoduodenectomy, left spleno-pancreatectomy, or total pancreatectomy according to the location and extent of the tumor. Standard lymphadenectomy will be performed as previously described. 15 Venous invasion is suspected by preoperative imaging and intraoperatively diagnosed in case of not dissociable adherence between the tumor and the PV/SMVaxis. The technique of venous resection and reconstruction includes tangential resection with primary suture or patch interposition, segmental resection with end-to-end venous anastomosis or venous graft interposition or vascular prosthesis interposition. Venous resection and reconstruction are defined according to the International Study Group of Pancreatic Surgery (ISGPS) as follows: type 1 = partial venous excision with direct closure (venorrhaphy) by suture closure; type 2 = partial venous excision using a patch; type 3 = segmental resection with primary veno-venous anastomosis; and type 4 = segmental resection with interpose venous conduit and at least two anastomoses. 16 The splenic vein will be ligated, or preserved, or ligated and reimplanted according to tumor location and surgeon s choice. The technique of vascular reconstruction and the type of pancreatic, biliary, and enteric anastomoses dependes on operating surgeon s choice.

Definition of Clinical Outcomes Postoperative complications are defined according to the ISGPS. Postoperative mortality are defined as death occurring during the first 30 days after surgery or during hospitalization. Overall survival is calculated from the date of surgery to the date of death. Pathological Examination Pathologists with specific experience on pancreatic oncology will examine the specimens. A microscopic positive resection margin (R1) is defined as presence of tumor cells within 1 mm from the margin in the absence of macroscopic evidence of residual tumor, which is classified as R2. Margins are classified according to the recommendation of the ISGPS. 15 Adjuvant Therapies and Follow-up Adjuvant chemotherapy or radiochemotherapy will be administered according to the evaluation of the multidisciplinary tumor board of each single institution, basing on performance status and tumor characteristics. Follow-up will consist on physical examination and CA 19-9 determination every 3 months and thoraco-abdominal CT scan every 6 months during the first 2 years. After 2 years physical examination, CA 19-9 determination and CT scan will be performed every 6 months. Statistical Analysis Data will be collected by every center and analyzed. Qualitative variables will be compared using the Chi square test, and quantitative variables will be analyzed using Student s t test. Univariate and multivariate analysis of factors related to histological venous invasion will be performed using logistic regression model. Multivariate analysis will include variables significant at univariate analysis. Univariate analysis of factors related to postoperative morbidity and mortality will be performed using logistic regression model. The survival rates will be estimated using the Kaplan Meier method. The log-rank test will be used to compare survival curves of subgroups, with continuous variables dichotomized around the median value. Multivariate proportional hazard regression (Cox model) analysis of prognostic factors will be performed. Two-sided P values will be computed; P\0.05 will be considered statistically significant. All analyses will be performed using MedCalc for Windows, version 10.2.0.0 (MedCalc Software, Belgium). REFERENCES

1. Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin. 2014;64:9-29. 2. NewEuropan CancerObservatory IARC; Cancer factsheets. http:// eco.iarc.fr/eucan/cancer.aspx?cancer=15. Accessed 13 July 2015. 3. Malvezzi M, Bertuccio P, Rosso T, Rota M, Levi F, La Vecchia C, Negri E. European cancer mortality predictions for the year 2015: does lung cancer have the highest death rate in EU women? Ann Oncol 2015;26:779 86. 4. Katz MH, Hwang R, Fleming JB, Evans DB. Tumor-nodemetastasis staging of pancreatic adenocarcinoma. CA Cancer J Clin 2008;58:111 25. 5. National Cancer Institute. SEER Cancer Statistics Review, 1975 2009 (Vintage 2009 Populations). http://seer.cancer.gov/csr/ 1975_2009_pops09/. Accessed 13 July 2015. 6. Tseng JF, Tamm EP, Lee JE, Pisters PW, Evans DB. Venous resection in pancreatic cancer surgery. Best Pract Res Clin Gastroenterol 2006;20:349 64. 7. Harrison LE, Klimstra DS, Brennan MF. Isolated portal vein involvement in pancreatic adenocarcinoma. A contraindication for resection? Ann Surg 1996;224:342 9. 8. Fuhrman GM, Leach SD, Staley CA, et al. Rationale for en bloc vein resection in the treatment of pancreatic adenocarcinoma adherent to the superior mesenteric-portal vein confluence. Pancreatic Tumor Study Group. Ann Surg 1996;223:154 62. 9. Ramacciato G, Mercantini P, Petrucciani N, et al. Does portalsuperior mesenteric vein invasion still indicate irresectability for pancreatic carcinoma? Ann Surg Oncol 2009;16:817 25. 10. Zhou Y, Zhang Z, Liu Y, Li B, Xu D. Pancreatectomy combined with superior mesenteric veinportal vein resection for pancreatic cancer: a meta-analysis. World J Surg 2012;36:884 91. 11. Fukuda S, Oussoultzoglou E, Bachellier P, Rosso E, Nakano H, Audet M, Jaeck D. Significance of the depth of portal vein wall invasion after curative resection for pancreatic adenocarcinoma. Arch Surg 2007;142:172 9. 12. Wang J, Estrella JS, Peng L, et al. Histologic tumor involvement of superior mesenteric vein/portal vein predicts poor prognosis in patients with stage II pancreatic adenocarcinoma treated with neoadjuvant chemoradiation. Cancer 2012;118:3801 11. 13. Okabayashi T, Shima Y, Iwata J, et al. Reconsideration about the aggressive surgery for resectable pancreatic cancer: a focus on real pathological portosplenomesenteric venous invasion. Langenbecks Arch Surg 2015;400:487 94. 14. G. Ramacciato, G. Nigri, N. Petrucciani, A D Pinna, M. Ravaioli, E. Jovine, F. Minni, G. L. Grazi, P. Chirletti, G. Tisone, N. Napoli, and U. Boggi. Pancreatectomy with Mesenteric and Portal Vein

Resection for Borderline Resectable Pancreatic Cancer: Multicenter Study of 406 Patients. Ann Surg Oncol. DOI 10.1245/s10434-016-5123-5 15. Tol JA, Gouma DJ, Bassi C, et al. Definition of a standard lymphadenectomy in surgery for pancreatic ductal adenocarcinoma: a consensus statement by the International Study Group on Pancreatic Surgery (ISGPS). Surgery 2014;156:591 600. 16. Bockhorn M, Uzunoglu FG, Adham M, et al. Borderline resectable pancreatic cancer: a consensus statement by the International Study Group of Pancreatic Surgery (ISGPS). Surgery 2014;155:977 88.