Diagnosis and management of gastrointestinal complications in adult cancer patients: 2017 updated evidence-based guidelines of the Infectious Diseases Working Party (AGIHO) of the German Society of Hematology and Medical Oncology (DGHO)
- PMID: 29177551
- PMCID: PMC5748412
- DOI: 10.1007/s00277-017-3183-7
Diagnosis and management of gastrointestinal complications in adult cancer patients: 2017 updated evidence-based guidelines of the Infectious Diseases Working Party (AGIHO) of the German Society of Hematology and Medical Oncology (DGHO)
Abstract
Cancer patients frequently suffer from gastrointestinal complications. In this manuscript, we update our 2013 guideline on the diagnosis and management of gastrointestinal complications in adult cancer patients by the Infectious Diseases Working Party (AGIHO) of the German Society of Hematology and Medical Oncology (DGHO). An expert group was put together by the AGIHO to update the existing guideline. For each sub-topic, a literature search was performed in PubMed, Medline, and Cochrane databases, and strengths of recommendation and the quality of the published evidence for major therapeutic strategies were categorized using the 2015 European Society for Clinical Microbiology and Infectious Diseases (ESCMID) criteria. Final recommendations were approved by the AGIHO plenary conference. Recommendations were made with respect to non-infectious and infectious gastrointestinal complications. Strengths of recommendation and levels of evidence are presented. A multidisciplinary approach to the diagnosis and management of gastrointestinal complications in cancer patients is mandatory. Evidence-based recommendations are provided in this updated guideline.
Keywords: Abdominal complications; Cancer; Chemotherapy; Colitis; Diarrhea; Infection.
Conflict of interest statement
Conflict of interest
DB is a consultant to Gilead Sciences and Merck Sharp & Dohme/Merck, received research grants from Gilead Sciences and Pfizer, honoraria for lectures from Astellas, Gilead Sciences, Merck Sharp & Dohme/Merck, Pfizer, and TEVA and travel grants from Astellas, Merck Sharp & Dohme/Merck, and Pfizer.
OAC is supported by the German Federal Ministry of Research and Education (BMBF grant 01KN0706), has received research grants from Astellas Pharma, Bayer, Basilea, Genzyme, Gilead Sciences, Pfizer, Merck, Optimer, Schering-Plough, Vicuron, has worked as a consultant for Astellas Pharma, Basilea, F2G, Gilead Sciences, Pfizer, Merck, Mölnlycke Health Care, Nektar Schering-Plough, Zeneus, and served at the speakers’ bureau of Schering-Plough, Astellas Pharma, Gilead Sciences, Merck, Pfizer, SpePharm and United Medical.
MH has served at the speakers` bureau of MSD, Roche, Novartis, Gilead Sciences, Boehringer Ingelheim, has received travels grants from MSD, Roche, Novartis, Gilead Sciences, Pfizer, Janssen-Cilag, and has served as a consultant for Takeda Pharma.
GM has served as a consultant for Gilead Sciences, MSD, Pfizer, Essex (Schering-Plough), Novartis and Sanofi-Aventis and has been on the Speakers’ Bureau for Gilead Sciences, MSD, Pfizer and Cephalon.
ES has received travel grants from Essex/Schering-Plough, Gilead, Janssen-Cilag, Merck/MSD, Novartis, Pfizer, Roche and Shire.
JV has received grants from Schering-Plough and Astellas Pharma, worked as a consultant for Pfizer and Schering-Plough, and served at the speakers’ bureau of Astellas Pharma, Gilead Sciences, Schering-Plough, Merck and Pfizer.
MJGTV is a consultant to: Berlin Chemie, MSD/Merck and Astellas Pharma; has served at the speakers’ bureau of: Astellas Pharma, Basilea, Gilead Sciences, Merck/MSD, Organobalance and Pfizer; received research funding from: 3M, Astellas Pharma, DaVolterra, Gilead Sciences, Merck/MSD, Organobalance, and Seres Therapeutics.
All remaining authors have declared no conflicts of interest.
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