Division of Oncology, Lombardi Comprehensive Cancer Center, Georgetown, University School of Medicine, Washington DC, 20007, USA.
The University of Texas Health Science Center School of Public Health, Houston, TX, 77030, USA.
BMC Cancer. 2018 Nov 27;18(1):1174. doi: 10.1186/s12885-018-5080-4.
Cachexia is a multisystem syndrome characterized by weight loss, anorexia, loss of muscle mass, systemic inflammation, insulin resistance, and functional decline. Management of cachexia involves addressing multiple underlying biological mechanisms. Previous review on pharmacological management of cancer cachexia identified progestins and corticosteroids as effective agents for treatment of cachexia. However, to date no consensus exists on a single effective or standard treatment for management of cachexia. The aim of this systematic review is to determine the effectiveness of pharmacological treatments used to manage cachexia among adult cancer patients.
We performed literature searches of PubMed (NLM), Embase (Ovid), and Medline(Ovid) to identify clinical trials focused on pharmacological management of cancer cachexia among adult cancer patients from 2004 to 2018. Three reviewers screened a random selection of abstracts to measure for interrater reliability. After this step, each screener screened two-thirds of all abstracts and 177 studies were identified for full text review. The primary outcome was impact of pharmacological management on change in either weight or lean body mass in cancer patients.
We identified 19 articles (representing 20 RCTs) that focused on pharmacological management of cancer cachexia. Agents showing promising results included Anamorelin and Enobosarm. Anamorelin at 50 or 100 mg per day for 12 weeks showed a consistent benefit across all studies and resulted in significant improvement in weight as compared to baseline among cancer patients. Enobosarm at 1 and 3 mg per day was also effective in improving lean body mass and QOL symptoms among advancer stage cancer patients. Finally, use of combination agents provide evidence for targeting multiple pathways underlying cachexia mechanism to achieve maximum benefit. No agents showed functional improvement in cancer patients.
Anamorelin as a single agent shows promising results in improving cachexia related weight loss among cancer patients. Further research on combination therapies may be helpful to address critical gaps in cachexia management.
恶病质是一种多系统综合征,其特征为体重减轻、厌食、肌肉量减少、全身炎症、胰岛素抵抗和功能下降。恶病质的治疗需要针对多种潜在的生物学机制。先前对癌症恶病质药物治疗的综述确定孕激素和皮质类固醇是治疗恶病质的有效药物。然而,迄今为止,尚无针对癌症恶病质管理的单一有效或标准治疗方法。本系统综述的目的是确定用于治疗成人癌症患者恶病质的药物治疗的有效性。
我们检索了 2004 年至 2018 年间在 PubMed(NLM)、Embase(Ovid)和 Medline(Ovid)上发表的关于成年癌症患者癌症恶病质药物治疗的临床试验。三位审查员随机筛选摘要以评估组内一致性。完成这一步骤后,每位筛查员筛选了三分之二的摘要,确定了 177 项研究进行全文审查。主要结局是药物治疗对癌症患者体重或瘦体重变化的影响。
我们共确定了 19 篇(代表 20 项 RCT)关注癌症恶病质药物治疗的文章。显示出有前途的结果的药物包括 Anamorelin 和 Enobosarm。每天服用 Anamorelin 50 或 100mg,连续 12 周,所有研究均显示出一致的益处,与基线相比,癌症患者的体重显著增加。每天服用 1 或 3mg 的 Enobosarm 也能有效改善晚期癌症患者的瘦体重和生活质量症状。最后,联合使用药物为针对恶病质机制的多个途径提供了证据,以达到最大的获益。没有药物显示出对癌症患者的功能改善。
单一药物 Anamorelin 显示出在改善癌症患者恶病质相关体重减轻方面有较好的效果。进一步研究联合治疗可能有助于解决恶病质管理中的关键差距。