Adenocarcinoma, Mucinous* / drug therapy ; Adenocarcinoma, Mucinous* / mortality ; Adenocarcinoma, Mucinous* / surgery ; Aged ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Chemotherapy, Adjuvant / methods ; Deoxycytidine / analogs & derivatives ; Deoxycytidine / therapeutic use ; Female ; Fluorouracil / therapeutic use ; Gemcitabine ; Humans ; Irinotecan / therapeutic use ; Leucovorin / therapeutic use ; Male ; Middle Aged ; Oxaliplatin / therapeutic use ; Pancreatic Intraductal Neoplasms* / drug therapy ; Pancreatic Intraductal Neoplasms* / mortality ; Pancreatic Intraductal Neoplasms* / surgery ; Pancreatic Neoplasms* / drug therapy ; Pancreatic Neoplasms* / mortality ; Pancreatic Neoplasms* / surgery ; Retrospective Studies
Abstract
This cohort study investigates the association of contemporary adjuvant chemotherapy regimens after resection in adenocarcinoma arising from intraductal papillary mucinous neoplasms (A-IPMNs) with overall survival. QuestionWhat is the survival benefit associated with contemporary adjuvant chemotherapy regimens after resection in adenocarcinoma arising from intraductal papillary mucinous neoplasms (A-IPMNs)?FindingsIn this cohort study among 1321 patients with A-IPMNs, adjuvant chemotherapy was not associated with improved overall survival, regardless of adjuvant chemotherapy type.MeaningContemporary adjuvant chemotherapy was not associated with improved overall survival, and a randomized clinical trial is indicated. ImportanceAdjuvant chemotherapy regimens may be administered after pancreatic resection for adenocarcinoma arising from intraductal papillary mucinous neoplasms (A-IPMNs), although the evidence supporting their use is limited.ObjectiveTo evaluate the survival benefit associated with contemporary adjuvant chemotherapy regimens after resection in A-IPMNs between 2017 and 2023.Design, Setting, and ParticipantsThis retrospective cohort study was an international, multicenter study with 69 participating centers across Europe, North America, South America, and the Asia-Pacific region. Patients undergoing resection for A-IPMNs were included. Data were analyzed from May to August 2025.InterventionContemporary adjuvant chemotherapy regimens, such as gemcitabine-capecitabine (GemCap); 5-fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFIRINOX), modified FOLFIRINOX (mFOLFIRINOX), and S-1.Main Outcome and MeasureOverall survival (months).ResultsAmong 1321 patients (median [IQR] age 70 [63 to 76] years; 713 males [54.0%] and 608 females [46.0%]), 781 patients (59.1%) received adjuvant chemotherapy, while in 181 patients (13.7%) it was omitted due to poor patient fitness. Of patients who received adjuvant chemotherapy, 568 patients (72.6%) received contemporary regimens, including GemCap (232 patients [29.7%]), FOLFIRINOX (176 patients [22.5%]), mFOLFIRINOX (71 patients [9.1%]), and S-1 (70 patients [9.0%]). The median (IQR) follow-up for the cohort was 64.2 (40.4 to 85.0) months, and the median overall survival was 73.8 months (95% CI, 66.4 to 81.9 months). After 90-day landmark analysis and exclusion of patients ineligible for chemotherapy, adjuvant chemotherapy vs no adjuvant chemotherapy (propensity score-matched populations, 243:243 patients) was not associated with improved overall survival (median, 82.3 months; 95% CI, 78.2 months to not applicable [NA] vs not reached; 95% CI, 75.3 months to NA; P = .58). Contemporary regimens vs no adjuvant chemotherapy (propensity score-matched populations, 309:309 patients) was not associated with longer survival, and a mean survival benefit greater than 4.2 months over 5 years was excluded (difference in restricted mean survival, 1.26 months; 95%, -1.72 to 4.24 months). Treatment outcomes did not vary by chemotherapy regimen or disease characteristic (eg, N stage or carbohydrate antigen 19-9 level).Conclusions and RelevanceIn this study, contemporary adjuvant chemotherapy was not associated with improved overall survival in A-IPMNs, and a randomized clinical trial is indicated.