Research
Studies In Progress
MANAGEMENT OF groove pancreatitis (paraduodenal pancreatitis)
Evaluation and effectiveness of non surgical treatments in management of symptomatic paraduodenal pancreatitis
Etude du Club Français du Pancréas
Investigateurs:
Dr Bertrand Napoléon, Hôpital Privé Jean Mermoz
Dr Christelle d’Engremont, CHU Besançon
Abstract :
Paraduodenal pancreatitis (PP) is now a well histologically defined entity. However its incidence is poorly known. A surgical series of patients recorded 3.5% of paraduodenal pancreatis among pancreatic resections (Vitali F, pancreas 2014). Chronic panctreatitis is present in 60% of cases (De Pretis N, pancreas 2017).
The treatment strategy is still poorly codified. In the past, pancreatic surgery was the only option but its morbidity leds to find another effective possibilities. Symptomatic treatments (analgesics, artificial nutrition), somatostatin analogs and endoscopic procedures are available options (Rebours V, Am J Gastroenterol 2007and Arvanitakis M, endoscopy 2014).
The aim of this multicentric retrospective study is to evaluate the therapeutic possibilities and their efficacity in the management of PP.
Key words : paraduodenal pancreatitis, groove pancreatitis, cystic dystrophy of the duodenal wall
Methods
Retrospective study
Multicentric study :
Investigators and centres: CHU Beaujon (Prof. REBOURS), CHU Besançon (Dr. D’ENGREMONT), CHU Nantes (Dr. LERHUN), Hôpital Privé Mermoz (Dr. NAPOLEON), CHU Marseille (Prof. BARTHET) and IPC (Dr. GIOVANINI), CHU Reims (Dr. DEFOUR), CHU Rouen (Dr. THOMASSIN), CHU Toulouse (Prof. BUSCAIL)
Inclusion criteria:
- All patients suffering from paraduodenal pancreatitis diagnosed by scan, MRI, echoendoscopy or pathological analysis of surgical specimens
- Symptomatic patients
- Between 2000 and 2020
Data collection:
- Demographic data: date of birth, sex, tobacco and alcohol consumption
- Clinical data: diabetes, pain, weight loss, vomiting, jaundice, haemorrhage, pancreatic exocrine insufficiency
- Morphological data: location of paraduodenal pancreatitis lesions, presence and number of cysts in duodenal wall, lesions of chronic pancreatitis (calcifications, ducts abnormalities, pancreatic atrophy…)
- Therapeutic approaches:
- - endoscopic treatment (pancreatic stenting, cyst fenestration….), ,
- - medical treatment: artificial nutrition, pain killers, analogues of somatostatine ….,
Main objective: to assess the efficacy of the treatments (pain relief relapse …)
HOW TO PARTICIPATE Contact us:
cdengremont@chu-besancon.fr
dr.napoleon@wanadoo.fr
CLINICAL AND RADIOLOGICAL GRADING SYSTEM FOR PREDICTING SEVERITY OF DYSPLASIA IN MUCINOUS CYSTADENOMA OF THE PANCREAS (MUCINOUS COHORT)
PaRaDis Reference Centre Project
Head of Coordinating Team:
Prof. Vinciane REBOURS (PU-PH) - Deputy Head of Department - Department of Gastroenterology and Pancreatology, Hôpital Beaujon
Chief Investigator:
Dr Lina AGUILERA MUNOZ - Hôpital Beaujon - Service gastro-entérologie et pancréatologie
Investigateurs:
Dr. Lucie LAURENT - Hôpital Beaujon - Department of Gastroenterology and Pancreatology
Prof. Marie Pierre VULLIERME - Hôpital Beaujon - Medical Imaging - Clichy (Centralized review of preoperative images)
Prof. Jerome CROS - Hôpital Beaujon - Anatomy and Pathology - (Centralized review of surgical tissue slides)
Other teams from the Rare Pancreatic Diseases Reference Centre (PaRaDis) who wish to participate.
Logistics: Sandra ROLLET, CRA PaRaDis - Hôpital Beaujon - Department of Gastroenterology and Pancreatology
SUMMARY
Mucinous Cystic Neoplasia (MCN) is a rare pancreatic cyst lesion, but also one of the three precancerous pancreatic conditions. Its natural history is unknown and diagnosis necessarily requires surgical resection.
It is possible that like intraductal papillary mucinous neoplasms of the pancreas, a majority of these cysts could be simply monitored, without systematic recourse to resection, thus avoiding the risks of major and long-term surgery. However, no predictive clinical or morphological criteria have been studied or evaluated to validate such an approach, and experts’ recommendations remain unclear as to the optimal attitude to adopt.
Main objective:
Obtain a predictive score for malignity of mucinous cystadenoma using the clinical and radiological information available at diagnosis. Malignity is defined by at least high-grade dysplasia, distinguished at time of histological analysis of the surgical tissue biopsy.
Secondary objectives:
- Evaluate overall survival with reference to the grade of dysplasia of the mucinous cystadenoma
- Assess the degree of post-operative complications
Methodology:
Retrospective multicentric cohort of approximately 300 patients
Inclusion criteria:
- 1. Patients having undergone surgery for pancreatic mucinous cystadenoma between January 2008 and September 2020 in a participating centre
- Histologically confirmed mucinous cystadenoma
- Pre-operative imaging available including TDM and/or MRI
Exclusion criteria :
- Histological material not available
- Absence of pre-operative TDM or MRI
- Patient refusal
Main data to be collected:
Age, sex, blood group ABO, use of tobacco, alcohol, weight and height, diabetes, personal history of pancreatitis, family or personal history of cancer (pancreas), gynaecology and obstetrics history;
CA level of 19.9 at diagnosis
Group ABO
Pre-operative TDM or MRI imaging will undergo centralized review via CD-ROM
Pathological reports
Post-operative complications: infection, fistula, haemorrhage etc.
Relapse of mucinous cystadenoma
Date of death
Cause of death
Main selection criteria:
- Presence of at least high-grade dysplasia in surgical biopsy tissue (confirmed after second reading)
Selection criteria/secondary assessment:
- Status alive or dead if known at time of biopsy collection.
- Complications, e.g., fistula, infection or haemorrhage post-operatively; i.e., within 30 days of resection
Analytical methods:
Assessment of predictive score for possibility of mucinous cystadenoma with at least high-grade dysplasia; initially, candidate factors will undergo univariate analysis (logistic regression model). Factors with a p-value <0.20 will be included in a multivariate model using a descending model with
p <0.05. The predictive score is derived from the regression coefficients of this multivariate logistic regression model.
How to participate ?
If you wish to participate in data collection for this cohort, please contact:
Dr Lina AGUILERA MUNOZ lina.aguileramunoz@aphp.fr
Sandra ROLLET (ARC) sandra.rollet@aphp.fr ou centre.paradis@aphp.fr Tél : 01 71 11 46 73
Publications From PaRaDis Members
Pancreatic Cysts
Do we need contrast agents for EUS?
Saftoiu A, Napoleon B, Arcidiacono PG, Braden B, Burmeister S, Carrara S, Cui XW, Fusaroli P, Gottschalk U, Hocke M, Hollerbach S, Iglesias-Garcia J, Jenssen C, Kitano M, Larghi A, Oppong KW, Sahai AV, Sun S, Burmester E, Di Leo M, Petrone MC, Santos E, Teoh AYB, Hwang JH, Rimbas M, Sharma M, Puri R, Kahaleh M, Dietrich CF.
Endosc Ultrasound. Nov-Dec 2020;9(6):361-368
Pancreatic cystic lesions: time to move to 19-gauge needle with EUS-guided microforceps biopsy or needle-based confocal laser endomicroscopy. [No abstract available]
Larghi A, Crinò SF, Napoleon B.
Gastrointest Endosc. 2020 Jul;92(1):222.
Palazzo M, Sauvanet A, Gincul R, Borbath I, Vanbiervliet G, Bourdariat R, Lemaistre AI, Pujol B, Caillol F, Palazzo L, Aubert A, Maire F, Buscail L, Giovannini M, Marque S, Napoléon B.
Surg Endos, 2020 Jun; 34(6), 2532-2540
Karsenti D, Palazzo L, Perrot B, Zago J, Lemaistre AI, Cros J, Napoléon B.
Endoscopy. 2020 May 14. doi: 10.1055/a-1160-5485.
Genomic profile concordance between pancreatic cyst fluid and neoplastic tissue.
Laquière AE, Lagarde A, Napoléon B, Bourdariat R, Atkinson A, Donatelli G, Pol B, Lecomte L, Curel L, Urena-Campos R, Helbert T, Valantin V, Mithieux F, Buono JP, Grandval P, Olschwang S.
World J Gastroenterol. 2019 Sep 28;25(36):5530-5542.
Napoleon B, Palazzo M, Lemaistre AI, Caillol F, Palazzo L, Aubert A, Buscail L, Maire F, Morellon BM, Pujol B, Giovannini M.
Endoscopy. 2019;51(9):825-835.
The Role of Endoscopic Ultrasound in the Diagnosis of Cystic Lesions of the Pancreas.
Lévy P, Rebours V.Visc Med. 2018 Jul;34(3):192-196. Review.
Diagnostic and Treatment Algorithms of Pancreatic Cystic Tumors. [No abstract available]
Werner J, Belyaev O, Fernández-Del Castillo C, Lévy P, Löhr M, Mayerle J, Uhl W.Visc Med. 2018 Jul;34(3):212-215.
European evidence-based guidelines on pancreatic cystic neoplasms.
European Study Group on Cystic Tumours of the Pancreas.
Gut. 2018 May;67(5):789-804
Serous cystic neoplasm of the pancreas: a multinational study of 2622 patients under the auspices of the International Association of Pancreatology and European Pancreatic Club (European Study Group on Cystic Tumors of the Pancreas).
Jais B, Rebours V, Malleo G, Salvia R, Fontana M, Maggino L, Bassi C, Manfredi R, Moran R, Lennon AM, Zaheer A, Wolfgang C, Hruban R, Marchegiani G, Fernández Del Castillo C, Brugge W, Ha Y, Kim MH, Oh D, Hirai I, Kimura W, Jang JY, Kim SW, Jung W, Kang H, Song SY, Kang CM, Lee WJ, Crippa S, Falconi M, Gomatos I, Neoptolemos J, Milanetto AC, Sperti C, Ricci C, Casadei R, Bissolati M, Balzano G, Frigerio I, Girelli R, Delhaye M, Bernier B, Wang H, Jang KT, Song DH, Huggett MT, Oppong KW, Pererva L, Kopchak KV, Del Chiaro M, Segersvard R, Lee LS, Conwell D, Osvaldt A, Campos V, Aguero Garcete G, Napoleon B, Matsumoto I, Shinzeki M, Bolado F, Fernandez JM, Keane MG, Pereira SP, Acuna IA, Vaquero EC, Angiolini MR, Zerbi A, Tang J, Leong RW, Faccinetto A, Morana G, Petrone MC, Arcidiacono PG, Moon JH, Choi HJ, Gill RS, Pavey D, Ouaïssi M, Sastre B, Spandre M, De Angelis CG, Rios-Vives MA, Concepcion-Martin M, Ikeura T, Okazaki K, Frulloni L, Messina O, Lévy P.Gut. 2016 Feb;65(2):305-12.
Quality assessment of the guidelines on cystic neoplasms of the pancreas. Pancreatology.
Falconi M, Crippa S, Chari S, Conlon K, Kim SW, Levy P, Tanaka M, Werner J, Wolfgang CL, Pezzilli R, Castillo CF.
2015 Sep-Oct;15(5):463-9. doi: 10.1016/j.pan.2015.05.478. Epub 2015 Jun 12Dokmak S, Aussilhou B, Rasoaherinomenjanahary F, Sauvanet A, Vullierme MP, Rebours V, Lévy P.
World J Gastroenterol. 2015 Jun 14;21(22):7047-51.
Differential Diagnosis of Cystic Pancreatic Lesions Including the Usefulness of Biomarkers.
Lévy P, Rebours V.
Viszeralmedizin. 2015 Feb;31(1):7-13. Review
Macrocystic pancreatic cystadenoma: The role of EUS and cyst fluid analysis in distinguishing mucinous and serous lesions.
O'Toole D, Palazzo L, Hammel P, Ben Yaghlene L, Couvelard A, Felce-Dachez M, Fabre M, Dancour A, Aubert A, Sauvanet A, Maire F, Levy P,Ruszniewski P.Gastrointest Endosc 2004;59:823-9.
Chronic Pancretitis
Analysis of GPRC6A variants in different pancreatitis etiologies.
Kaune T, Ruffert C, Hesselbarth N, Damm M, Krug S, Cardinal von Widdern J, Masson E, Chen JM, Rebours V, Buscail L, Férec C, Grützmann R, Te Morsche RHM, Drenth JP, Cavestro GM, Zuppardo RA, Saftoiu A, Malecka-Panas E, Głuszek S, Bugert P, Lerch MM, Sendler M, Weiss FU, Zou WB, Deng SJ, Liao Z, Scholz M, Kirsten H, Hegyi P, Witt H, Michl P, Griesmann H, Rosendahl J.Pancreatology. 2020 Oct;20(7):1262-1267.
International consensus guidelines on interventional endoscopy in chronic pancreatitis. Recommendations from the working group for the international consensus guidelines for chronic pancreatitis in collaboration with the International Association of Pancreatology, the American Pancreatic Association, the Japan Pancreas Society, and European Pancreatic Club.
Kitano M, Gress TM, Garg PK, Itoi T, Irisawa A, Isayama H, Kanno A, Takase K, Levy M, Yasuda I, Lévy P, Isaji S, Fernandez-Del Castillo C, Drewes AM, Sheel ARG, Neoptolemos JP, Shimosegawa T, Boermeester M, Wilcox CM, Whitcomb DC.Pancreatology. 2020 Sep;20(6):1045-1055.
International consensus guidelines on the role of diagnostic endoscopic ultrasound in the management of chronic pancreatitis. Recommendations from the working group for the international consensus guidelines for chronic pancreatitis in collaboration with the International Association of Pancreatology, the American Pancreatic Association, the Japan Pancreas Society, and European Pancreatic Club.
Mel Wilcox C, Gress T, Boermeester M, Masamune A, Lévy P, Itoi T, Varadarajulu S, Irisawa A, Levy M, Kitano M, Garg P, Isaji S, Shimosegawa T, Sheel ARG, Whitcomb DC, Neoptolemos JP; International (IAP-APA-JPS-EPC) Consensus Guidelines for Chronic Pancreatitis.Pancreatology. 2020 Jul;20(5):822-827.
Masamune A, Kotani H, Sörgel FL, Chen JM, Hamada S, Sakaguchi R, Masson E, Nakano E, Kakuta Y, Niihori T, Funayama R, Shirota M, Hirano T, Kawamoto T, Hosokoshi A, Kume K, Unger L, Ewers M, Laumen H, Bugert P, Mori MX, Tsvilovskyy V, Weißgerber P, Kriebs U, Fecher-Trost C, Freichel M, Diakopoulos KN, Berninger A, Lesina M, Ishii K, Itoi T, Ikeura T, Okazaki K, Kaune T, Rosendahl J,Nagasaki M, Uezono Y, Algül H, Nakayama K, Matsubara Y, Aoki Y, Férec C, Mori Y, Witt H, Shimosegawa T.
Gastroenterology. 2020 May;158(6):1626-1641.
Hegyi P, Párniczky A, Lerch MM, Sheel ARG, Rebours V, Forsmark CE, Del Chiaro M, Rosendahl J, de-Madaria E, Szücs Á, Takaori K, Yadav D, Gheorghe C, Rakonczay Z Jr, Molero X, Inui K, Masamune A, Fernandez-Del Castillo C, Shimosegawa T, Neoptolemos JP, Whitcomb DC, Sahin-Tóth M; Working Group for the International (IAP – APA – JPS – EPC) Consensus Guidelines for Chronic Pancreatitis
Pancreatology. 2020 Jun;20(4):579-585.
Kleeff J, Whitcomb DC, Shimosegawa T, Esposito I, Lerch MM, Gress T, Mayerle J, Drewes AM, Rebours V, Akisik F, Muñoz JED, Neoptolemos JP.
Nat Rev Dis Primers. 2017 Sep 7;3:17060. Review
Epidemiology of chronic pancreatitis: burden of the disease and consequences.
Lévy P, Domínguez-Muñoz E, Imrie C, Löhr M, Maisonneuve P.
United European Gastroenterol J. 2014 Oct;2(5):345-54.Genetics and pathogenesis of chronic pancreatitis: the 2012 update.
Chen JM, Férec C.
Clin Res Hepatol Gastroenterol. 2012 Aug;36(4):334-40.An overview of hereditary pancreatitis.
Rebours V, Lévy P, RuszniewskiP.
Dig Liver Dis. 2012 Jan;44(1):8-15. Review
Pathology analysis reveals that dysplastic pancreatic ductal lesions are frequent in patients with hereditary pancreatitis.
Rebours V, Lévy P, Mosnier JF, Scoazec JY, Soubeyrand MS, Fléjou JF, Turlin B, Hammel P, Ruszniewski P, Bedossa P, Couvelard A.Clin Gastroenterol Hepatol. 2010 Feb;8(2):206-12.
Mortality rate and risk factors in patients with hereditary pancreatitis: uni- and multidimensional analyses.
Rebours V, Boutron-Ruault MC, Jooste V, Bouvier AM, Hammel P, Ruszniewski P, Lévy PAm J Gastroenterol. 2009 Sep;104(9):2312-7.
Chronic pancreatitis: genetics and pathogenesis.
Chen JM, Férec C.
Annu Rev Genomics Hum Genet. 2009;10:63-87.The natural history of hereditary pancreatitis: a national series.
Rebours V, Boutron-Ruault MC, Schnee M, Férec C, Le Maréchal C, Hentic O,Maire F, Hammel P, Ruszniewski P, Lévy P.Gut 2009;58:97-103.
From the chronic pancreatitis to chronic pancreatites.
Maire F, Lévy P, Rebours V, Hammel P, Ruszniewski P.
Gastroenterol Clin Biol. 2009 Aug-Sep;33(8-9):725-36.
Diagnosis and management of chronic pancreatitis.
Buscail L.
Rev Prat. 2002 Sep 15;52(14):1561-6.Hereditary Pancreatitis related to PRSS1 and PRSS2 Mutations
The variable phenotype of the p.A16V mutation of cationic trypsinogen (PRSS1) in pancreatitis families.
Grocock CJ, Rebours V, Delhaye MN, Andrén-Sandberg A, Weiss FU, Mountford R, Harcus MJ, Niemczyck E, Vitone LJ, Dodd S, Jørgensen MT, Ammann RW, Schaffalitzky de Muckadell O, Butler JV, Burgess P, Kerr B, Charnley R, Sutton R, Raraty MG, Devière J, Whitcomb DC, Neoptolemos JP, Lévy P, Lerch MM, Greenhalf W; European Registry of Hereditary Pancreatitis and Pancreatic Cancer.Gut. 2010 Mar;59(3):357-63.
A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis.
Witt H, Sahin-Tóth M, Landt O, Chen JM, Kähne T, Drenth JP, Kukor Z, Szepessy E, Halangk W, Dahm S, Rohde K, Schulz HU, Le Maréchal C, Akar N, Ammann RW, Truninger K, Bargetzi M, Bhatia E, Castellani C, Cavestro GM, Cerny M, Destro-Bisol G, Spedini G, Eiberg H, Jansen JB, Koudova M, Rausova E, Macek M Jr, Malats N, Real FX, Menzel HJ, Moral P, Galavotti R, Pignatti PF, Rickards O, Spicak J, Zarnescu NO, Böck W, Gress TM, Friess H, Ockenga J, Schmidt H, Pfützer R, Löhr M, Simon P, Weiss FU, Lerch MM, Teich N, Keim V, Berg T, Wiedenmann B, Luck W, Groneberg DA, Becker M, Keil T, Kage A, Bernardova J, Braun M, Güldner C, Halangk J, Rosendahl J, Witt U, Treiber M, Nickel R, Férec C.
Nat Genet. 2006 Jun;38(6):668-73.Genetic Pancreatitis related to CFTR Mutations
Ivacaftor CFTR Potentiator Therapy is Efficient for Pancreatic Manifestations in Cystic Fibrosis.
Kounis I, Lévy P, Rebours V.
Am J Gastroenterol. 2018 Jul;113(7):1058-1059.
Pelletier AL, Bienvenu T, Rebours V, O'Toole D, Hentic O, Maire F, Hammel P, Ruszniewski P, Lévy P.
Pancreatology. 2010;10(2-3):158-64.
Etude prospective de la fréquence des mutations du gène CFTR chez des malades ayant une pancréatite idiopathique.
Maire F, Bienvenu T, Ngukam A, Hammel P, Ruszniewski P, Lévy P.Gastroenterol Clin Biol 2003;27:398-402.
Pediatric Population
Mercier C, Pioche M, Albuisson E, Ponchon T, Gonzalez JM, Barthet M, Boytchev I, Vanbiervliet G, Fortier Beaulieu C, Prat F, Belle A, Branche J, Grandval P, Valats JC, Rudler F, Wallenhorst T, Koch S, Comte A, Williet N, Musquer N, Coron E, Derosiere A, Le Mouel JP, Schaefer M, Chabot C, Scheers I, Deprez PH, Chevaux JB.
Endoscopy. 2020 Jun 29.
Revue Douleurs: Evaluation - Diagnostic - Traitement, Volume 19, Issue 4, pe7-e8, 159-204 (September 2018)
Genetic Pancreatitis related to SPINK1 mutations
Clinical interpretation of SPINK1 and CTRC variants in pancreatitis.
Girodon E, Rebours V, Chen JM, Pagin A, Levy P, Ferec C, Bienvenu T.
Pancreatology. 2020 Oct;20(7):1354-1367.Natural history of SPINK1 germline mutation related-pancreatitis.
Muller N, Sarantitis I, Rouanet M, de Mestier L, Halloran C, Greenhalf W, Férec C,Masson E, Ruszniewski P, Lévy P, Neoptolemos J, Buscail L, Rebours V.
EBioMedicine. 2019 Oct;48:581-591.
Severe infantile isolated exocrine pancreatic insufficiency caused by the complete functional loss of the SPINK1 gene.
Venet T, Masson E, Talbotec C, Billiemaz K, Touraine R, Gay C, Destombe S, Cooper DN, Patural H, Chen JM, Férec C.
Hum Mutat. 2017 Dec;38(12):1660-1665.Functional analysis of eight missense mutations in the SPINK1 gene. [No abstract available]
Boulling A, Keiles S, Masson E, Chen JM,Férec C.Pancreas. 2012 Mar;41(2):329-30
Assessing the pathological relevance of SPINK1 promoter variants.
Boulling A, Witt H, Chandak GR, Masson E, Paliwal S, Bhaskar S, Reddy DN, Cooper DN, Chen JM, Férec C.
Eur J Hum Genet. 2011 Oct;19(10):1066-73.Baudry C, Rebours V, Houillier P, Hammel P, Ruszniewski P, Levy P.
Pancreas. 2010 Apr;39(3):420-1.
Genetic Pancreatitis related to CTRC mutations
Association of rare chymotrypsinogen C (CTRC) gene variations in patients with idiopathic chronic pancreatitis.
Masson E, Chen JM, Scotet V, Le Maréchal C, Férec C.
Hum Genet. 2008 Feb;123(1):83-91.