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The evolution of clinical outcomes in metastatic pancreatic adenocarcinoma: a 10-year experience at a tertiary referral center.
Ellithi, Moataz; Abdallah, Mohamed; Fischer, McKenna; Ailts, Isaak; Fanta, John; Waligoske, Kate; Bell, Matthew; Nelson, Morgan E; Bleeker, Jonathan.
Affiliation
  • Ellithi M; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South Dakota, USA.
  • Abdallah M; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South Dakota, USA.
  • Fischer M; Department of Medicine, University of Minnesota, Minneapolis, Mn, USA.
  • Ailts I; Department of Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South DakotaSouth Dakota, USA.
  • Fanta J; Department of Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South DakotaSouth Dakota, USA.
  • Waligoske K; Department of Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South DakotaSouth Dakota, USA.
  • Bell M; Department of Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South DakotaSouth Dakota, USA.
  • Nelson ME; Department of Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South DakotaSouth Dakota, USA.
  • Bleeker J; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South Dakota, USA.
Expert Rev Gastroenterol Hepatol ; 16(5): 479-486, 2022 May.
Article in En | MEDLINE | ID: mdl-35400291
BACKGROUND: Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer mortality in the US. Recent studies have demonstrated survival benefits for FOLFIRINOX (5-FU, leucovorin, irinotecan, and oxaliplatin) and Gem/nab-P (gemcitabine/nab-paclitaxel) over gemcitabine. We aimed to evaluate the clinical outcomes of mPDAC before and after incorporating these newer regimens into the clinical practice. METHODS: A retrospective study of patients with mPDAC at our institution between 2009 and 2018, who were followed up until December 2019. Overall survival (OS) and progression-free survival (PFS) were calculated using Kaplan-Meier survival analysis. Univariate and multivariable Cox regression analyses were used to explore predictors of survival. RESULTS: A total of 394 patients with mPDAC were included: 122 (31%) were diagnosed 2009-2013 and 272 (69%) 2014-2018. In 2009-2013 cohort vs. 2014-2018 cohort, the median OS and PFS were similar (4 vs. 3.6 months, P = 0.5) and (2.3 vs. 2.5 months, P = 0.41), respectively. Age, ECOG-PS >1, serum albumin, neutrophil-to-lymphocyte ratio, and platelets-to-lymphocyte ratio were independent predictors of better OS. CONCLUSIONS: In this study of real-world data, the median OS and PFS for all patients with mPDAC were equivalent before and after incorporating newer treatment regimens into the clinical practice.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Adenocarcinoma Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Expert Rev Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Adenocarcinoma Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Expert Rev Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom