Abstract

In cancer patients, loss of muscle mass is significantly associated with low tolerability of chemotherapy and poor survival. Despite the great strides in the treatment of cancer, targeted therapies such as tyrosine kinase inhibitors (TKIs) could exacerbate muscle wasting. Over recent years, the impact of skeletal muscle loss during TKI therapy on clinical outcomes has been in the spotlight. In this review, we focus on the different molecular pathways of TKIs potentially involved in muscle wasting. Then, we report the results of the studies assessing the effects of different TKI therapies—such as sorafenib, regorafenib, sunitinib, and lenvatinib—on muscle mass, and highlight their potential clinical implications. Finally, we discuss an integrative nutritional approach to be adopted during TKI treatment. The assessment of muscle mass from computerized tomography imaging could be helpful in predicting toxicity and prognosis in patients treated with TKI such as sorafenib. Early recognition of low muscle mass and effective personalized nutritional support could prevent or attenuate muscle mass wasting. However, the role of nutrition is still overlooked, and future clinical trials are needed to find the optimal nutritional support to countermeasure muscle mass depletion during TKI therapy.

Highlights

  • The discovery of the overexpression of kinases in various cancers has led to the development of tyrosine kinase inhibitors (TKIs)

  • Just to name a few examples, imatinib has revolutionized the treatment of chronic myelogenous leukemia as well as gastrointestinal stromal tumors (GISTs) [1]; sorafenib was the first therapy proven to prolong survival in patients with metastatic hepatocellular carcinoma (HCC) [2]; sunitinib provided for the first time a survival advantage over interferon to treat metastatic renal cell cancer (RCC) [3]

  • After focusing on the specific molecular pathways of TKI involved in muscle wasting, we review the impact of TKI therapy on muscle mass for several types of cancer and its implications in terms of clinical outcomes

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Summary

Introduction

The discovery of the overexpression of kinases in various cancers has led to the development of tyrosine kinase inhibitors (TKIs). TKIs demonstrated to produce a significant improvement in survival rates in several cancers. Low skeletal muscle mass was already shown to be a significant predictor of chemotherapy toxicity and survival in cancer patients [5,6,7]. A growing number of studies attempted to understand whether muscle wasting was exacerbated by TKI treatment and if such muscle loss was associated with toxicity and survival outcomes. This review aims to understand how TKI therapy could impact muscle mass in cancer patients and highlights potential clinical implications and nutritional opportunities. After focusing on the specific molecular pathways of TKI involved in muscle wasting, we review the impact of TKI therapy on muscle mass for several types of cancer and its implications in terms of clinical outcomes. We discuss the state of the art about nutritional strategies to counteract muscle wasting during these treatments

Molecular Pathways of TKI Involved in Muscle Wasting
Impact of TKI Treatment on Muscle Wasting
Method of Muscle Mass
Sorafenib
Lenvatinib
Sunitinib
Regorafenib
Pazopanib
Axitinib
Vandetanib
Thyroid Cancer
Early Assessment and Monitoring of Nutritional Status During Treatment
Personalized Nutritional Support
Conclusions
Findings
Methods
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