Adjuvant chemotherapy for adenocarcinoma arising from intraductal papillary mucinous neoplasia: multicentre ADENO-IPMN study.
Author
Lucocq, JamesHawkyard, Jake
Haugk, Beate
Mownah, Omar
Menon, Krishna
Furukawa, Takaki
Inoue, Yosuke
Hirose, Yuki
Sasahira, Naoki
Feretis, Michael
Balakrishnan, Anita
Ceresa, Carlo
Davidson, Brian
Pande, Rupaly
Dasari, Bobby
Tanno, Lulu
Karavias, Dimitrios
Helliwell, Jack
Young, Alistair
Nunes, Quentin
Urbonas, Tomas
Silva, Michael
Gordon-Weeks, Alex
Barrie, Jenifer
Gomez, Dhanny
van Laarhoven, Stijn
Robertson, Francis
Nawara, Hossain
Doyle, Joseph
Bhogal, Ricky
Harrison, Ewen
Roalso, Marcus
Ciprani, Debora
Aroori, Somaiah
Ratnayake, Bathiya
Koea, Jonathan
Capurso, Gabriele
Bellotti, Ruben
Stättner, Stefan
Alsaoudi, Tareq
Bhardwaj, Neil
Rajesh, Srujan
Jeffery, Fraser
Connor, Saxon
Cameron, Andrew
Jamieson, Nigel
Sheen, Amy
Mittal, Anubhav
Samra, Jas
Gill, Anthony
Roberts, Keith
Søreide, Kjetil
Pandanaboyana, Sanjay
Publication date
2024-04-03
Metadata
Show full item recordAbstract
Background: The clinical impact of adjuvant chemotherapy after resection for adenocarcinoma arising from intraductal papillary mucinous neoplasia is unclear. The aim of this study was to identify factors related to receipt of adjuvant chemotherapy and its impact on recurrence and survival. Methods: This was a multicentre retrospective study of patients undergoing pancreatic resection for adenocarcinoma arising from intraductal papillary mucinous neoplasia between January 2010 and December 2020 at 18 centres. Recurrence and survival outcomes for patients who did and did not receive adjuvant chemotherapy were compared using propensity score matching. Results: Of 459 patients who underwent pancreatic resection, 275 (59.9%) received adjuvant chemotherapy (gemcitabine 51.3%, gemcitabine-capecitabine 21.8%, FOLFIRINOX 8.0%, other 18.9%). Median follow-up was 78 months. The overall recurrence rate was 45.5% and the median time to recurrence was 33 months. In univariable analysis in the matched cohort, adjuvant chemotherapy was not associated with reduced overall (P = 0.713), locoregional (P = 0.283) or systemic (P = 0.592) recurrence, disease-free survival (P = 0.284) or overall survival (P = 0.455). Adjuvant chemotherapy was not associated with reduced site-specific recurrence. In multivariable analysis, there was no association between adjuvant chemotherapy and overall recurrence (HR 0.89, 95% c.i. 0.57 to 1.40), disease-free survival (HR 0.86, 0.59 to 1.30) or overall survival (HR 0.77, 0.50 to 1.20). Adjuvant chemotherapy was not associated with reduced recurrence in any high-risk subgroup (for example, lymph node-positive, higher AJCC stage, poor differentiation). No particular chemotherapy regimen resulted in superior outcomes. Conclusion: Chemotherapy following resection of adenocarcinoma arising from intraductal papillary mucinous neoplasia does not appear to influence recurrence rates, recurrence patterns or survival.Citation
Lucocq J, Hawkyard J, Haugk B, Mownah O, Menon K, Furukawa T, Inoue Y, Hirose Y, Sasahira N, Feretis M, Balakrishnan A, Ceresa C, Davidson B, Pande R, Dasari B, Tanno L, Karavias D, Helliwell J, Young A, Nunes Q, Urbonas T, Silva M, Gordon-Weeks A, Barrie J, Gomez D, Van Laarhoven S, Robertson F, Nawara H, Doyle J, Bhogal R, Harrison E, Roalso M, Ciprani D, Aroori S, Ratnayake B, Koea J, Capurso G, Bellotti R, Stättner S, Alsaoudi T, Bhardwaj N, Rajesh S, Jeffery F, Connor S, Cameron A, Jamieson N, Sheen A, Mittal A, Samra J, Gill A, Roberts K, Søreide K, Pandanaboyana S. Adjuvant chemotherapy for adenocarcinoma arising from intraductal papillary mucinous neoplasia: multicentre ADENO-IPMN study. Br J Surg. 2024 Apr 3;111(4):znae100. doi: 10.1093/bjs/znae100. PMID: 38659247.Type
ArticleOther
PMID
38659247Journal
British Journal of SurgeryPublisher
Oxford University Pressae974a485f413a2113503eed53cd6c53
10.1093/bjs/znae100