恶病质
医学
浪费的
厌食症
癌症
临床试验
肌萎缩
食欲
合成代谢
药物治疗
生物信息学
胰岛素抵抗
内科学
肿瘤科
胰岛素
生物
作者
Guilherme Wesley Peixoto da Fonseca,Ryosuke Sato,Maria Janieire de Nazaré Nunes Alves,Stephan von Haehling
标识
DOI:10.1080/14656566.2023.2194489
摘要
Introduction Cancer cachexia is a multifactorial metabolic syndrome associated with a pathophysiology intertwined with increased inflammatory response, anorexia, metabolic dysregulation, insulin resistance, and hormonal alterations, which together generate a negative energy balance in favor of catabolism. The development of therapeutic strategies to treat cancer cachexia has always been related to clinical interventions with increased food intake/supplementation, physical exercise regimens, and/or medication to attenuate catabolism and increase the anabolic response. However, the approval of drugs by regulatory agencies has always been a challenge.Areas covered This review outlines the main pharmacotherapy findings in cancer cachexia as well as the ongoing clinical trials that have evaluated changes in body composition and muscle function. The National Library of Medicine (PubMed) was used as search tool.Expert opinion The pharmacological therapy for cachexia should be focused on improving body composition, muscle function, and mortality, although none of the compounds used so far was able to demonstrate positive results beyond increased appetite and improvements in body composition. Ponsegromab (GDF15 inhibitor), a new compound that has just entered a phase II clinical trial, is a promising candidate to treat cancer cachexia and may produce exciting results if the study can be conducted as planned.
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