Understanding the mechanisms and treatment options in cancer cachexia

被引:681
作者
Fearon, Kenneth [1 ]
Arends, Jann [2 ]
Baracos, Vickie [3 ]
机构
[1] Univ Edinburgh, Sch Clin Sci & Community Hlth, Royal Infirm, Edinburgh EH16 45A, Midlothian, Scotland
[2] Univ Freiburg, Tumour Biol Ctr, D-79106 Freiburg, Germany
[3] Univ Alberta, Dept Oncol, Div Palliat Care Med, Edmonton, AB T6G 1Z2, Canada
关键词
CELL LUNG-CANCER; SKELETAL-MUSCLE HYPERTROPHY; WEIGHT-LOSS; BODY-COMPOSITION; DOUBLE-BLIND; CLINICAL-IMPLICATIONS; NUTRITIONAL SUPPORT; ENERGY-EXPENDITURE; PHYSICAL-ACTIVITY; ORAL SUPPLEMENT;
D O I
10.1038/nrclinonc.2012.209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer cachexia is a metabolic syndrome that can be present even in the absence of weight loss ('precachexia'). Cachexia is often compounded by pre-existing muscle loss, and is exacerbated by cancer therapy. Furthermore, cachexia is frequently obscured by obesity, leading to under-diagnosis and excess mortality. Muscle wasting (the signal event in cachexia) is associated not only with reduced quality of life, but also markedly increased toxicity from chemotherapy. Many of the primary events driving cachexia are likely mediated via the central nervous system and include inflammation-related anorexia and hypoanabolism or hypercatabolism. Treatment of cachexia should be initiated early. In addition to active management of secondary causes of anorexia (such as pain and nausea), therapy should target reduced food intake (nutritional support), inflammation-related metabolic change (anti-inflammatory drugs or nutrients) and reduced physical activity (resistance exercise). Advances in the understanding of the molecular biology of the brain, immune system and skeletal muscle have provided novel targets for the treatment of cachexia. The combination of therapies into a standard multimodal package coupled with the development of novel therapeutics promises a new era in supportive oncology whereby quality of life and tolerance to cancer therapy could be improved considerably. Fearon, K. et.al. Nat. Rev. Clin. Oncol. 10, 90-99 (2013); published online 4 December 2012; doi:10.1038/nrclinonc.2012.209
引用
收藏
页码:90 / 99
页数:10
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