Emerging new therapeutic alternatives for the management of cancer cachexia: recent insights

Abstract

To the Editor: Garcia et al. have provided interesting data in their recent article [1]. New compounds have been identified recently that may play a significant role in mitigating cancer cachexia. BL-6020/979 has recently been shown to attenuate cancer cachexia. It mediates its effect by antagonizing melanocortin-4 receptor function [2]. Its administration significantly improves food intake. At the same time, energy expenditure is attenuated significantly. In addition, it is orally effective and demonstrates depression mitigating properties. Another drug with considerable potential is ARA286. It is an erythropoietin analogue that significantly attenuates muscle loss in cancer cachexia models [3]. Another drug that has shown effectiveness in mitigating cancer cachexia is theophylline; it mediates its effect by attenuating cachexia-associated proteolysis [4]. As a result there is a reduction in serum TNF-alpha levels. MT-102 is another emerging alternative with considerable efficacy. It is an anabolic/ catabolic transforming agent that reduces muscle loss in cancer cachexia. The ACT-ONE study is currently underway to see if these anabolic effects can be illustrated in humans also [5]. Similarly, rosiglitazone has recently been shown to attenuate cancer-associated cachexia; it results in marked improvement in adipose tissue mass. It also restores PPARdelta in muscles to their normal levels [6]. A similar effect is seen on muscle PDK4 levels. As a result, it delays cachexia-associated weight loss. Another recent alternative is tocilizumab. It is an antiinterleukin-6 receptor antibody that has shown effectiveness in reducing the signs and symptoms of cancer-associated cachexia [7]. It enhances retinol-binding protein levels. At the same time, pre-albumin levels are also accentuated. Ursolic acid has also been recently shown to reduce cancer cachexia. It is a natural triterpene that mediates its effect by accentuating skeletal muscle insulin: IGF-1 signaling [8]. At the same time, it attenuates the expression of atrophy related mRNAs. The above-mentioned agents have shown considerable promise so far. Hopefully, the coming few years will see further research to fully evaluate their role in mitigating cancer cachexia.