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阿那莫林之后接下来是什么?

What is next after anamorelin?

作者信息

Garcia Jose M

机构信息

aGeriatric Research, Education and Clinical Center (GRECC), VA Puget Sound Healthcare System bDepartment of Medicine, Division of Gerontology & Geriatric Medicine, University of Washington School of Medicine, Seattle, Washington, USA.

出版信息

Curr Opin Support Palliat Care. 2017 Dec;11(4):266-271. doi: 10.1097/SPC.0000000000000299.

Abstract

PURPOSE OF REVIEW

In spite of its relevance, treatments for the cancer anorexia and cachexia syndrome (CACS) are not available. One of the agents that recently reached phase III clinical trials is anamorelin. Its development, along with that of other agents for this indication, will be reviewed here, with a focus on the gaps in the current knowledge and future directions.

RECENT FINDINGS

In spite of several targets showing promising results in early development, their difficulties obtaining regulatory approval underscore the need to reconsider the current strategies in drug development and the challenges in the field of CACS.

SUMMARY

Further research is needed in order to meet the challenges of developing treatments for CACS. Preclinical studies should expand our understanding about key regulators of appetite, muscle, and energy metabolism in this setting using models that can be translated reliably to humans. Clinical research efforts should focus on validating the entry criteria, endpoints, outcomes, and the potential synergistic effects and interaction between different targets, nutrition, and exercise interventions. Clinical meaningfulness and significance should be taken into account in the design of clinical trials. It is essential that all key stakeholders are included in the design of future strategies.

摘要

综述目的

尽管癌症恶病质综合征(CACS)相关治疗具有重要意义,但目前仍缺乏有效的治疗方法。阿那莫林是一种最近进入III期临床试验的药物。本文将回顾其研发情况以及其他针对该适应症的药物的研发情况,重点关注当前知识的空白和未来的发展方向。

最新研究成果

尽管有几个靶点在早期研发中显示出有希望的结果,但它们在获得监管批准方面遇到的困难凸显了重新审视当前药物研发策略以及CACS领域所面临挑战的必要性。

总结

为应对开发CACS治疗方法的挑战,需要进一步开展研究。临床前研究应利用能够可靠地转化为人体模型的方法,加深我们对该情况下食欲、肌肉和能量代谢关键调节因子的理解。临床研究工作应专注于验证入组标准、终点指标、结局以及不同靶点、营养和运动干预之间潜在的协同效应和相互作用。在临床试验设计中应考虑临床意义和重要性。至关重要的是,所有关键利益相关者都应参与未来策略的设计。

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