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Serum cytokine profiles in patients with pancreatic cancer and chronic pancreatitis.
Lanki, Mira; Mustonen, Harri; Salmi, Marko; Jalkanen, Sirpa; Haglund, Caj; Seppänen, Hanna.
Afiliação
  • Lanki M; Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland; Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Finland. Electronic address: mira.lanki@helsinki.fi.
  • Mustonen H; Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. Electronic address: harri.mustonen@helsinki.fi.
  • Salmi M; MediCity Research Laboratory, University of Turku, Turku, Finland. Electronic address: masalmi@utu.fi.
  • Jalkanen S; MediCity Research Laboratory, University of Turku, Turku, Finland. Electronic address: sirjal@utu.fi.
  • Haglund C; Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland; Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Finland. Electronic address: caj.haglund@hus.fi.
  • Seppänen H; Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland; Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Finland. Electronic address: hanna.seppanen@hus.fi.
Pancreatology ; 23(6): 657-662, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37468364
BACKGROUND: Chronic pancreatitis (CP) may cause tumor-like lesions, creating a challenge in distinguishing between CP and pancreatic ductal adenocarcinoma (PDAC) in a patient. Given that invasive surgery is a standard cancer treatment, we aimed to examine whether a noninvasive diagnostic tool utilizing serum cytokines could safely differentiate between PDAC and CP. METHODS: A pre-operative serum panel comprising 48 inflammatory cytokines, CA19-9, and C-reactive protein (CRP) was analyzed, consisting of 231 patients, 186 with stage I-III PDAC and 45 with CP. We excluded PDAC patients who underwent neoadjuvant therapy and those CP patients with other active malignancies. The laboratory variables most associated with PDAC diagnosis were assessed using logistic regression and selected using the lasso method. RESULTS: The cytokines CTACK, GRO-α, and ß-NGF were selected alongside CA19-9 and CRP for our differential diagnostic model. The area under the curve (AUC) for our differential diagnostic model was 0.809 (95% confidence interval [CI] 0.738-0.880), compared with 0.791 (95% CI 0.728-0.854) for CA19-9 alone (not significant). CONCLUSIONS: We found that inflammatory cytokines CTACK, GRO-α, and ß-NGF alongside CA19-9 and CRP may help distinguish PDAC from CP.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Pancreatite Crônica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Pancreatology Assunto da revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Pancreatite Crônica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Pancreatology Assunto da revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Ano de publicação: 2023 Tipo de documento: Article