| Literature DB >> 33588150 |
M Haas1, D T Waldschmidt2, M Stahl3, A Reinacher-Schick4, J Freiberg-Richter5, L Fischer von Weikersthal6, F Kaiser7, S Kanzler8, N Frickhofen9, T Seufferlein10, T Dechow11, R Mahlberg12, P Malfertheiner13, G Illerhaus14, S Kubicka15, A Abdul-Ahad16, R Snijder16, S Kruger17, C B Westphalen17, S Held18, M von Bergwelt-Baildon17, S Boeck17, V Heinemann17.
Abstract
BACKGROUND: Targeting the epidermal growth factor receptor pathway remains controversial in pancreatic cancer. Afatinib is an oral irreversible ErbB family blocker approved in non-small-cell lung cancer. This open-label, multicenter, randomised phase II trial evaluated gemcitabine plus afatinib (Gem/afatinib) versus gemcitabine (Gem) alone as first-line treatment for metastatic pancreatic cancer. PATIENTS AND METHODS: Patients were randomised in a 2:1 ratio to either Gem (1000 mg/m2 weekly for three weeks followed by one week of rest, repeated every four weeks) and afatinib (40 mg orally once daily) or Gem alone. Overall survival (OS) was the primary study end-point. The novel BOTh©™ methodology was implemented to derive a quantitative estimate for the 'Burden of Therapy/Toxicity' (BOTh) for each patient on every day during the clinical study.Entities:
Keywords: Afatinib; Burden of therapy/toxicity; Chemotherapy; Gemcitabine; Pancreatic cancer
Year: 2021 PMID: 33588150 DOI: 10.1016/j.ejca.2020.12.029
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162