001     301547
005     20250524113308.0
024 7 _ |a 10.1007/s00423-025-03735-3
|2 doi
024 7 _ |a pmid:40402347
|2 pmid
024 7 _ |a 0023-8236
|2 ISSN
024 7 _ |a 1435-2443
|2 ISSN
024 7 _ |a 0174-4542
|2 ISSN
024 7 _ |a 0367-0023
|2 ISSN
024 7 _ |a 1432-1491
|2 ISSN
024 7 _ |a 1435-2451
|2 ISSN
037 _ _ |a DKFZ-2025-01068
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Hüttner, Felix J
|b 0
245 _ _ |a Pancreatic resection with perioperative drug repurposing of propranolol and etodolac - the phase II randomized controlled PROSPER trial.
260 _ _ |a Heidelberg
|c 2025
|b Springer
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1748004803_18334
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a The perioperative period is characterized by psychological stress and inflammatory reactions that can contribute to disease recurrence or metastatic spread. These reactions are mediated particularly by catecholamines and prostaglandins. The PROSPER trial aimed to evaluate whether a perioperative drug repurposing with a non-selective betablocker (propranolol) and a COX-2 inhibitor (etodolac) is feasible and safe in the setting of pancreatic cancer surgery.Patients undergoing partial pancreatoduodenectomy for pancreatic cancer were randomized to perioperative treatment with propranolol and etodolac or placebo. Main safety endpoint was the rate of serious adverse events (SAE) and the main feasibility endpoint was adherence. Overall and disease-free survival (DFS) as well as recurrences were assessed as efficacy parameters and the trial was accompanied by a translational study.The trial was prematurely closed due to slow recruitment. 26 patients were randomized, but 6 never started trial medication. Finally, 9 patients received the trial medication and 11 patients placebo. There were 6 SAE in the treatment vs. 14 in the placebo group. Adherence was lower in the treatment group, but without statistically significance. Median DFS was 16.36 months (95%-CI 1.18 - not reached) in verum vs. 11.25 (95%-CI 2.2 - 17.25) in placebo group. The rate of distant recurrences was 11.1% in verum vs. 54.5% in placebo group.There were no safety concerns, but the trial intervention was not feasible given slow recruitment and limited adherence. However, the translational study and preliminary efficacy data revealed some promising findings, warranting further investigation.DRKS00014054.
536 _ _ |a 314 - Immunologie und Krebs (POF4-314)
|0 G:(DE-HGF)POF4-314
|c POF4-314
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a Betablockade
|2 Other
650 _ 7 |a COX-2-inhibition
|2 Other
650 _ 7 |a Inflammation
|2 Other
650 _ 7 |a Pancreatic cancer
|2 Other
650 _ 7 |a Perioperative period
|2 Other
650 _ 7 |a Etodolac
|0 2M36281008
|2 NLM Chemicals
650 _ 7 |a Propranolol
|0 9Y8NXQ24VQ
|2 NLM Chemicals
650 _ 7 |a Cyclooxygenase 2 Inhibitors
|2 NLM Chemicals
650 _ 7 |a Adrenergic beta-Antagonists
|2 NLM Chemicals
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Pancreatic Neoplasms: surgery
|2 MeSH
650 _ 2 |a Pancreatic Neoplasms: mortality
|2 MeSH
650 _ 2 |a Pancreatic Neoplasms: pathology
|2 MeSH
650 _ 2 |a Pancreatic Neoplasms: drug therapy
|2 MeSH
650 _ 2 |a Etodolac: therapeutic use
|2 MeSH
650 _ 2 |a Drug Repositioning
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Propranolol: therapeutic use
|2 MeSH
650 _ 2 |a Pancreaticoduodenectomy
|2 MeSH
650 _ 2 |a Cyclooxygenase 2 Inhibitors: therapeutic use
|2 MeSH
650 _ 2 |a Adrenergic beta-Antagonists: therapeutic use
|2 MeSH
650 _ 2 |a Perioperative Care: methods
|2 MeSH
700 1 _ |a Klotz, Rosa
|b 1
700 1 _ |a Giese, Nathalia A
|b 2
700 1 _ |a Kong, Bo
|b 3
700 1 _ |a Ahmed, Azaz
|0 P:(DE-He78)bac8c2c56238485ecf0475ff14438430
|b 4
|u dkfz
700 1 _ |a Merz, Daniela
|b 5
700 1 _ |a Pöchmann, Alexandra
|0 P:(DE-He78)3ca80d09e9dd0c1e6adb522a70caf051
|b 6
|u dkfz
700 1 _ |a Burghaus, Ina
|b 7
700 1 _ |a Hackert, Thilo
|b 8
700 1 _ |a Strobel, Oliver
|b 9
700 1 _ |a Mihaljevic, André L
|b 10
700 1 _ |a Michalski, Christoph W
|b 11
700 1 _ |a Büchler, Markus W
|b 12
700 1 _ |a Diener, Markus K
|b 13
773 _ _ |a 10.1007/s00423-025-03735-3
|g Vol. 410, no. 1, p. 168
|0 PERI:(DE-600)1459390-7
|n 1
|p 168
|t Langenbeck's archives of surgery
|v 410
|y 2025
|x 0023-8236
909 C O |o oai:inrepo02.dkfz.de:301547
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 4
|6 P:(DE-He78)bac8c2c56238485ecf0475ff14438430
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 6
|6 P:(DE-He78)3ca80d09e9dd0c1e6adb522a70caf051
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-314
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Immunologie und Krebs
|x 0
914 1 _ |y 2025
915 _ _ |a DEAL Springer
|0 StatID:(DE-HGF)3002
|2 StatID
|d 2024-12-05
|w ger
915 _ _ |a DEAL Springer
|0 StatID:(DE-HGF)3002
|2 StatID
|d 2024-12-05
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1110
|2 StatID
|b Current Contents - Clinical Medicine
|d 2024-12-05
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2024-12-05
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b LANGENBECK ARCH SURG : 2022
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2024-12-05
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2024-12-05
915 _ _ |a IF < 5
|0 StatID:(DE-HGF)9900
|2 StatID
|d 2024-12-05
920 1 _ |0 I:(DE-He78)D196-20160331
|k D196
|l Translationale Immuntherapie
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)D196-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21