Background: Intraductal oncocytic papillary neoplasms (IOPNs) of the pancreas are now considered a separate entity to intraductal papillary mucinous neoplasms (IPMN). Invasive IOPNs are extremely rare, and their recurrence patterns, response to adjuvant chemotherapy and long-term survival outcomes are unknown. Methods: Consecutive patients undergoing pancreatic resection (2010–2020) for invasive IOPNs or adenocarcinoma arising from IPMN (A-IPMN) from 18 academic pancreatic centers worldwide were included. Outcomes of invasive IOPNs were compared with A-IPMN invasive subtypes (ductal and colloid A-IPMN). Results: 415 patients were included: 20 invasive IOPN, 331 ductal A-IPMN and 64 colloid A-IPMN. After a median follow-up of 6-years, 45% and 60% of invasive IOPNs had developed recurrence and died, respectively. There was no significant difference in recurrence or overall survival between invasive IOPN and ductal A-IPMN. Overall survival of invasive IOPNs was inferior to colloid A-IPMNs (median time of survival 24.4 months vs. 86.7, months, p = 0.013), but the difference in recurrence only showed borderline significance (median time to recurrence, 22.5 months vs. 78.5 months, p = 0.132). Adjuvant chemotherapy, after accounting for high-risk features, did not reduce rates of recurrence in invasive IOPN (p = 0.443), ductal carcinoma (p = 0.192) or colloid carcinoma (p = 0.574). Conclusions: Invasive IOPNs should be considered an aggressive cancer with a recurrence rate and prognosis consistent with ductal type A-IPMN.

Invasive intraductal oncocytic papillary neoplasms (IOPN) and adenocarcimoma arising from intraductal papillary mucinous neoplasms (A-IPMN) of the pancreas: comparative analysis of clinicopathological features, patterns of recurrence and survival: a multicentre study / Lucocq, J.; Haugk, B.; Joseph, N.; Hawkyard, J.; White, S.; Mownah, O.; Menon, K.; Furukawa, T.; Inoue, Y.; Hirose, Y.; Sasahira, N.; Mittal, A.; Samra, J.; Sheen, A.; Feretis, M.; Balakrishnan, A.; Ceresa, C.; Davidson, B.; Pande, R.; Dasari, B. V. M.; Tanno, L.; Karavias, D.; Helliwell, J.; Young, A.; Nunes, Q.; Urbonas, T.; Silva, M.; Gordon-Weeks, A.; Barrie, J.; Gomez, D.; Van Laarhoven, S.; Nawara, H.; Doyle, J.; Bhogal, R.; Harrison, E.; Roalso, M.; Zaharia, C.; Ciprani, D.; Aroori, S.; Ratnayake, B.; Koea, J.; Capurso, G.; Bellotti, R.; Stattner, S.; Alsaoudi, T.; Bhardwaj, N.; Jeffery, F.; Connor, S.; Cameron, A.; Jamieson, N.; Roberts, K.; Soreide, K.; Gill, A. J.; Pandanaboyana, S.. - In: HPB. - ISSN 1365-182X. - 26:11(2024), pp. 1421-1428. [10.1016/j.hpb.2024.07.410]

Invasive intraductal oncocytic papillary neoplasms (IOPN) and adenocarcimoma arising from intraductal papillary mucinous neoplasms (A-IPMN) of the pancreas: comparative analysis of clinicopathological features, patterns of recurrence and survival: a multicentre study

Capurso G.;
2024-01-01

Abstract

Background: Intraductal oncocytic papillary neoplasms (IOPNs) of the pancreas are now considered a separate entity to intraductal papillary mucinous neoplasms (IPMN). Invasive IOPNs are extremely rare, and their recurrence patterns, response to adjuvant chemotherapy and long-term survival outcomes are unknown. Methods: Consecutive patients undergoing pancreatic resection (2010–2020) for invasive IOPNs or adenocarcinoma arising from IPMN (A-IPMN) from 18 academic pancreatic centers worldwide were included. Outcomes of invasive IOPNs were compared with A-IPMN invasive subtypes (ductal and colloid A-IPMN). Results: 415 patients were included: 20 invasive IOPN, 331 ductal A-IPMN and 64 colloid A-IPMN. After a median follow-up of 6-years, 45% and 60% of invasive IOPNs had developed recurrence and died, respectively. There was no significant difference in recurrence or overall survival between invasive IOPN and ductal A-IPMN. Overall survival of invasive IOPNs was inferior to colloid A-IPMNs (median time of survival 24.4 months vs. 86.7, months, p = 0.013), but the difference in recurrence only showed borderline significance (median time to recurrence, 22.5 months vs. 78.5 months, p = 0.132). Adjuvant chemotherapy, after accounting for high-risk features, did not reduce rates of recurrence in invasive IOPN (p = 0.443), ductal carcinoma (p = 0.192) or colloid carcinoma (p = 0.574). Conclusions: Invasive IOPNs should be considered an aggressive cancer with a recurrence rate and prognosis consistent with ductal type A-IPMN.
2024
Inglese
HPB
Elsevier B.V.
26
11
1421
1428
8
Pubblicato
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
Invasive intraductal oncocytic papillary neoplasms (IOPN) and adenocarcimoma arising from intraductal papillary mucinous neoplasms (A-IPMN) of the pancreas: comparative analysis of clinicopathological features, patterns of recurrence and survival: a multicentre study / Lucocq, J.; Haugk, B.; Joseph, N.; Hawkyard, J.; White, S.; Mownah, O.; Menon, K.; Furukawa, T.; Inoue, Y.; Hirose, Y.; Sasahira, N.; Mittal, A.; Samra, J.; Sheen, A.; Feretis, M.; Balakrishnan, A.; Ceresa, C.; Davidson, B.; Pande, R.; Dasari, B. V. M.; Tanno, L.; Karavias, D.; Helliwell, J.; Young, A.; Nunes, Q.; Urbonas, T.; Silva, M.; Gordon-Weeks, A.; Barrie, J.; Gomez, D.; Van Laarhoven, S.; Nawara, H.; Doyle, J.; Bhogal, R.; Harrison, E.; Roalso, M.; Zaharia, C.; Ciprani, D.; Aroori, S.; Ratnayake, B.; Koea, J.; Capurso, G.; Bellotti, R.; Stattner, S.; Alsaoudi, T.; Bhardwaj, N.; Jeffery, F.; Connor, S.; Cameron, A.; Jamieson, N.; Roberts, K.; Soreide, K.; Gill, A. J.; Pandanaboyana, S.. - In: HPB. - ISSN 1365-182X. - 26:11(2024), pp. 1421-1428. [10.1016/j.hpb.2024.07.410]
none
54
info:eu-repo/semantics/article
262
Lucocq, J.; Haugk, B.; Joseph, N.; Hawkyard, J.; White, S.; Mownah, O.; Menon, K.; Furukawa, T.; Inoue, Y.; Hirose, Y.; Sasahira, N.; Mittal, A.; Samr...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/198603
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