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治疗癌症恶病质的研究性药物:重点关注 I 期和 II 期临床试验。

Investigational drugs for the treatment of cancer cachexia: a focus on phase I and phase II clinical trials.

机构信息

a Department of Translational and Precision Medicine, Sapienza University of Rome , Rome , Italy.

b Department of Surgical Sciences, Sapienza University of Rome , Rome , Italy.

出版信息

Expert Opin Investig Drugs. 2019 Aug;28(8):733-740. doi: 10.1080/13543784.2019.1646727. Epub 2019 Jul 26.

Abstract

: Cachexia is frequent in chronic diseases and especially during cancer development. Multiple definitions of cachexia have been proposed; it may be considered a multifactorial complex syndrome that presents with progressive unintentional weight loss and wasting of muscle mass and adipose tissue. : This article covers phase-I and phase-II clinical trials of investigational drugs for cancer cachexia. We performed a search on PubMed with keywords as cancer cachexia, phase-I/phase-II trial, drug, identifying articles relevant to this review. Studies were conducted using compounds, including anabolic agents such as ghrelin analogs, selective androgen receptor modulators, as well as anti-inflammatory drugs such as thalidomide, OHR, anti-interleukin antibody, cannabinoids, and omega-3 supplements. We also describe the mechanisms of action of these molecules and their phase-I and phase-II study design. The major outcomes were appetite stimulation, weight gain, improvement of muscle mass and function, modulation of inflammation, and quality of life. : The molecules discussed act on molecular pathways involved in cancer cachexia; they modulate appetite, anabolic effects, inflammation and direct interaction with muscle. Considering the multifactorial aspects of the cachexia syndrome, the combination of these drugs with metabolic and nutritional interventions may represent the most promising therapeutic approach to cancer cachexia.

摘要

恶病质在慢性疾病中很常见,尤其是在癌症发展过程中。恶病质有多种定义;它可能被认为是一种多因素复杂的综合征,表现为进行性非有意的体重减轻和肌肉质量及脂肪组织的消耗。

本文涵盖了用于癌症恶病质的研究性药物的 I 期和 II 期临床试验。我们在 PubMed 上使用了关键词“癌症恶病质、I 期/II 期试验、药物”进行搜索,以确定与本综述相关的文章。研究使用了化合物,包括促生长素类似物、选择性雄激素受体调节剂等合成代谢剂,以及沙利度胺、OHR、抗白细胞介素抗体、大麻素和欧米伽-3 补充剂等抗炎药物。我们还描述了这些分子的作用机制及其 I 期和 II 期研究设计。主要结果是食欲刺激、体重增加、肌肉质量和功能改善、炎症调节以及生活质量。

讨论的分子作用于涉及癌症恶病质的分子途径;它们调节食欲、合成代谢作用、炎症,并与肌肉直接相互作用。考虑到恶病质综合征的多因素方面,这些药物与代谢和营养干预的联合可能代表治疗癌症恶病质最有前途的方法。

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