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Efficacy and Toxicity of 5-Fluorouracil-Oxaliplatin in Gastroenteropancreatic Neuroendocrine Neoplasms.
Merola, Elettra; Dal Buono, Arianna; Denecke, Timm; Arsenic, Ruza; Pape, Ulrich-Frank; Jann, Henning; Wiedenmann, Bertram; Pavel, Marianne E.
Afiliação
  • Dal Buono A; Digestive Endoscopy Unit, Division of Gastroenterology, Humanitas Clinical and Research Center, Rozzano Milan, Italy.
  • Arsenic R; Department of Pathology, Charité Mitte.
  • Jann H; Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Charité Mitte, Charité Universitätsmedizin, Berlin.
  • Wiedenmann B; Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Charité Mitte, Charité Universitätsmedizin, Berlin.
Pancreas ; 49(7): 912-917, 2020 08.
Article em En | MEDLINE | ID: mdl-32658073
OBJECTIVES: The objective of this study was to investigate the efficacy and tolerability of 5-fluorouracil-oxaliplatin (FOLFOX) in advanced gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). METHODS: Retrospective analysis of consecutive 72 advanced GEP-NENs treated with FOLFOX between 2005 and 2016 at a single German referral center for NENs was performed. We assessed treatment response by response evaluation criteria in solid tumors 1.0 criteria, progression-free survival by Kaplan-Meyer method, and risk factor analysis by Cox-regression model. RESULTS: Patients were 44.5% G1/G2, 55.5% G3, receiving a median of 7 treatment cycles (range, 2-21), and had a median of 18 months of follow-up (range, 3-111 months). Disease control was achieved in 75.0% of cases but 91.3% in the 23 patients receiving FOLFOX as first line (P = 0.04). Median progression-free survival of the overall population was 8 months. A better outcome was significantly related to treatment duration (P = 0.02) and grade of histological differentiation for G3 patients (well differentiated vs poorly differentiated, P = 0.03). Adverse events occurred in 88.8% of patients, mostly grade 1 and 2 hematotoxicity and chemotherapy-induced peripheral sensory neuropathy (84.1% and 50.0% of patients, respectively). CONCLUSIONS: Our results support FOLFOX as therapeutic option in advanced GEP-NENs with poor prognosis, either at first or further therapy line. Longer duration of therapy was associated with a more durable benefit.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Protocolos de Quimioterapia Combinada Antineoplásica / Tumores Neuroendócrinos / Neoplasias Gastrointestinais Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Protocolos de Quimioterapia Combinada Antineoplásica / Tumores Neuroendócrinos / Neoplasias Gastrointestinais Idioma: En Ano de publicação: 2020 Tipo de documento: Article