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Early recognition of malnutrition and cachexia in the cancer patient: A position paper of a European School of Oncology Task Force

  • M. Aapro
  • , J. Arends
  • , F. Bozzetti
  • , Ken Fearon*
  • , S. M. Grunberg
  • , J. Herrstedt
  • , J. Hopkinson
  • , N. Jacquelin-Ravel
  • , A. Jatoi
  • , S. Kaasa
  • , F. Strasser
  • *Corresponding author for this work

    Research output: Contribution to journal › Review › Research › peer-review

    Abstract

    Background: Weight loss and cachexia are common, reduce tolerance of cancer treatment and the likelihood of response, and independently predict poor outcome. Methods: A group of experts met under the auspices of the European School of Oncology to review the literature and- on the basis of the limited evidence at present-make recommendations for malnutrition and cachexia management and future research. Conclusions: Our focus should move from end-stage wasting to supporting patients' nutritional and functional state throughout the increasingly complex and prolonged course of anti-cancer treatment. When inadequate nutrient intake predominates (malnutrition), this can be managed by conventional nutritional support. In the presence of systemic inflammation/ altered metabolism (cachexia), a multi-modal approach including novel therapeutic agents is required. For all patients, oncologists should consider three supportive care issues: ensuring sufficient energy and protein intake, maintaining physical activity to maintain muscle mass and (if present) reducing systemic inflammation. The results of phase II/III trials based on novel drug targets (e.g. cytokines, ghrelin receptor, androgen receptor, myostatin) are expected in the next 2 years. If effective therapies emerge, early detection of malnutrition and cachexia will be increasingly important in the hope that timely intervention can improve both patient-centered and oncology outcomes.

    Original languageEnglish
    Article numbermdu085
    Pages (from-to)1492-1499
    Number of pages8
    JournalAnnals of Oncology
    Volume25
    Issue number8
    DOIs
    Publication statusPublished - Aug 2014

    Funding

    The European School of Oncology (ESO) Sharing Progress in Cancer Care programme has funded the meeting of the Task Force and covered the cost of the medical writer. KF has received speaker fees, advisory board fees or grant funding from Abbott, Nutricia, Helsinn, Novartis, Ono and Acacia Pharmaceuticals. MA has had recent relationships with the following companies: Abraxis, Amgen, AstraZeneca, Bayer-Schering, Bristol-Myers, Celgene, Cephalon, Chugai, Ferring, GSK, Helsinn, Hospira, Ipsen, Johnson and Johnson, Ortho Biotech, Merck Serono, Novartis, Pfizer, Pierre-Fabre, Roche, Sandoz, Schering, Sanofi, Teva and Vifor. AJ has had recent relationships with the following companies: GTX (served as a consultant); Incyte (was affiliated with a research network that accrued to one of its trials); Entera Health (received research funding); Helsinn Pharmaceuticals (served as a consultant); and X Biotech (received research funding). AJ has had recent relationships with the following companies: GTX (served as a consultant); Incyte (was affiliated with a research network that accrued to one of its trials); Entera Health (received research funding); Helsinn Pharmaceuticals (served as a consultant); and X Biotech (received research funding). MA is/has been a consultant for Amgen, Astellas, BMS, Celegene, GSK, Helsinn, Hospira, Novartis, Merck, Merck Serono, Pfizer, Pharmacosmos, Pierre Fabre, Roche, Sandoz, Teva, Vifor, and has received honoraria for lectures at symposia of Amgen, Bayer Schering, Cephalon, GSK, Helsinn, Hospira, JnJ OrthoBiotech, Merck, Merck Serono, Novartis, Pfizer, Pierre Fabre, Roche, Sandoz, Sanofi Aventis, Teva, Vifor. KF has received speaker fees, advisory board fees or grant funding from Abbott, Nutricia, Helsinn, Novartis, Ono, and Acacia Pharmaceuticals. All other authors have declared no conflicts of interest.

    Keywords

    • Cancer cachexia
    • Malnutrition
    • Nutritional support
    • Review
    • Systemic inflammation

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