Literature DB >> 33588150

Afatinib plus gemcitabine versus gemcitabine alone as first-line treatment of metastatic pancreatic cancer: The randomised, open-label phase II ACCEPT study of the Arbeitsgemeinschaft Internistische Onkologie with an integrated analysis of the 'burden of therapy' method.

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.
RESULTS: One hundred nineteen patients from 25 centres were randomised, 79 patients for Gem/afatinib and 40 for Gem. Median OS was 7.3 months in the Gem/afatinib arm versus 7.4 months in the Gem-alone arm (hazard ratio [HR]: 1.06, p = 0.80). Median progression-free survival was identical in both arms (3.9 months versus 3.9 months, HR: 0.85, p = 0.43). Adverse events were more frequent in the Gem/afatinib arm, especially diarrhoea (71% vs. 13%) and skin rash (65% vs. 5%). The BOTh©™ analysis revealed a significantly higher burden of toxicity in the combination arm (p = 0.0005).
CONCLUSION: The addition of afatinib to Gem did not improve treatment efficacy and was more toxic. The BOTh©™ methodology allowed a detailed insight into the course of treatment-related adverse events over the study period. The trial was registered at clinicaltrials.gov (NCT01728818) and Eudra-CT (2011-004063-77).
Copyright © 2021 Elsevier Ltd. All rights reserved.

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


  3 in total

1.  Identifying Outcomes of Patients With Advanced Pancreatic Adenocarcinoma and RECIST Stable Disease Using Radiomics Analysis.

Authors:  Qiuxia Yang; Yize Mao; Hui Xie; Tao Qin; Zhijun Mai; Qian Cai; Hailin Wen; Yong Li; Rong Zhang; Lizhi Liu
Journal:  JCO Precis Oncol       Date:  2022-03

2.  Preanalytical Variables in the Analysis of Mitochondrial DNA in Whole Blood and Plasma from Pancreatic Cancer Patients.

Authors:  Hannah Randeu; Abel J Bronkhorst; Zsuzsanna Mayer; Angela Oberhofer; Eleni Polatoglou; Volker Heinemann; Michael Haas; Stefan Boeck; Stefan Holdenrieder
Journal:  Diagnostics (Basel)       Date:  2022-08-06

3.  Identification of a lncRNA based signature for pancreatic cancer survival to predict immune landscape and potential therapeutic drugs.

Authors:  Di Ma; Yuchen Yang; Qiang Cai; Feng Ye; Xiaxing Deng; Baiyong Shen
Journal:  Front Genet       Date:  2022-09-14       Impact factor: 4.772

  3 in total

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