Suppr超能文献

晚期肝细胞癌患者接受酪氨酸激酶抑制剂治疗期间的骨骼肌损失

Skeletal Muscle Loss during Tyrosine Kinase Inhibitor Treatment for Advanced Hepatocellular Carcinoma Patients.

作者信息

Uchikawa Shinsuke, Kawaoka Tomokazu, Namba Maiko, Kodama Kenichiro, Ohya Kazuki, Morio Kei, Nakahara Takashi, Murakami Eisuke, Tsuge Masataka, Hiramatsu Akira, Imamura Michio, Takahashi Shoichi, Chayama Kazuaki, Aikata Hiroshi

机构信息

Department of Gastroenterology and Metabolism, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.

出版信息

Liver Cancer. 2020 Apr;9(2):148-155. doi: 10.1159/000503829. Epub 2019 Nov 8.

Abstract

INTRODUCTION

The measurement of body composition such as the skeletal muscle index (SMI) has been reported to be useful for predicting prognosis in hepatocellular carcinoma (HCC). In this study, we analyzed skeletal muscle change during sorafenib and lenvatinib therapy and the association between SMI and prognosis.

METHODS

A total of 67 patients with advanced HCC and Child-Pugh grade A status treated with tyrosine kinase inhibitors (TKIs) at Hiroshima University between September 2009 and December 2018 were enrolled in this retrospective cohort study. Patients underwent computed tomography (CT) imaging before starting sorafenib treatment and 1-3 months after treatment initiation.

RESULTS

In all patients, the median SMI was 45.3 cm/m before TKI treatment and 42.1 cm/m after treatment; 54 of 67 (80.6%) patients experienced SMI loss. The median ΔSMI was -1.5 cm/m/months, and no difference in ΔSMI was observed between patients receiving sorafenib and lenvatinib. No significant differences were observed in median ΔSMI between patients with and without progressive disease (-2.35 and -1.1 cm/m/months, respectively), albumin-bilirubin grade 1 and 2 group disease (-1.7 and -1.5 cm/m/months, respectively), and relative dose intensity ≤80 and >80 (-1.8 and -1.2 cm/m/months, respectively).

CONCLUSION

This report demonstrated that patients receiving TKI treatment experienced a significant loss of skeletal muscle mass regardless of disease progression, hepatic reserve, or which TKI (sorafenib or lenvatinib) they received.

摘要

引言

据报道,测量身体成分如骨骼肌指数(SMI)有助于预测肝细胞癌(HCC)的预后。在本研究中,我们分析了索拉非尼和仑伐替尼治疗期间骨骼肌的变化以及SMI与预后之间的关系。

方法

本回顾性队列研究纳入了2009年9月至2018年12月期间在广岛大学接受酪氨酸激酶抑制剂(TKIs)治疗的67例晚期HCC且Child-Pugh A级的患者。患者在开始索拉非尼治疗前及治疗开始后1 - 3个月接受计算机断层扫描(CT)成像。

结果

所有患者中,TKI治疗前SMI中位数为45.3 cm/m,治疗后为42.1 cm/m;67例患者中有54例(80.6%)出现SMI下降。SMI中位数变化(ΔSMI)为-1.5 cm/m/月,接受索拉非尼和仑伐替尼治疗的患者之间ΔSMI无差异。疾病进展患者与未进展患者之间(分别为-2.35和-1.1 cm/m/月)、白蛋白-胆红素分级1组和2组患者之间(分别为-1.7和-1.5 cm/m/月)以及相对剂量强度≤80和>80的患者之间(分别为-1.8和-1.2 cm/m/月)的ΔSMI均无显著差异。

结论

本报告表明,接受TKI治疗的患者无论疾病进展、肝脏储备情况或接受哪种TKI(索拉非尼或仑伐替尼),均出现骨骼肌质量显著下降。

相似文献

1
Skeletal Muscle Loss during Tyrosine Kinase Inhibitor Treatment for Advanced Hepatocellular Carcinoma Patients.
Liver Cancer. 2020 Apr;9(2):148-155. doi: 10.1159/000503829. Epub 2019 Nov 8.
6
Strategy for advanced hepatocellular carcinoma based on liver function and portal vein tumor thrombosis.
Hepatol Res. 2020 Dec;50(12):1375-1385. doi: 10.1111/hepr.13567. Epub 2020 Sep 26.
7
8
Impact of Grip Strength in Patients with Unresectable Hepatocellular Carcinoma Treated with Lenvatinib.
Cancers (Basel). 2020 Aug 3;12(8):2146. doi: 10.3390/cancers12082146.
9

引用本文的文献

2
Paradoxical Effect of Myosteatosis on the Immune Checkpoint Inhibitor Response in Metastatic Renal Cell Carcinoma.
J Cachexia Sarcopenia Muscle. 2025 Apr;16(2):e13758. doi: 10.1002/jcsm.13758.
3
Sorafenib induces cachexia by impeding transcriptional signaling of the SET1/MLL complex on muscle-specific genes.
iScience. 2024 Sep 10;27(10):110913. doi: 10.1016/j.isci.2024.110913. eCollection 2024 Oct 18.
5
Association between metabolic dysfunction-associated steatotic liver disease and myosteatosis measured by computed tomography.
J Cachexia Sarcopenia Muscle. 2024 Oct;15(5):1942-1952. doi: 10.1002/jcsm.13543. Epub 2024 Jul 16.
7
The New Era of Systemic Treatment for Hepatocellular Carcinoma: From the First Line to the Optimal Sequence.
Curr Oncol. 2023 Sep 26;30(10):8774-8792. doi: 10.3390/curroncol30100633.
10
Frailty in chronic myeloid leukemia: evidence from 2016-2018 Nationwide Inpatient Sample of the US.
BMC Geriatr. 2023 May 30;23(1):334. doi: 10.1186/s12877-023-03962-7.

本文引用的文献

1
4
Prognostic significance of sarcopenia in patients with hepatocellular carcinoma undergoing sorafenib therapy.
Oncol Lett. 2017 Aug;14(2):1637-1647. doi: 10.3892/ol.2017.6287. Epub 2017 May 31.
5
Fibroblast growth factor 19 regulates skeletal muscle mass and ameliorates muscle wasting in mice.
Nat Med. 2017 Aug;23(8):990-996. doi: 10.1038/nm.4363. Epub 2017 Jun 26.
6
Autophagy and Mitophagy in Cardiovascular Disease.
Circ Res. 2017 May 26;120(11):1812-1824. doi: 10.1161/CIRCRESAHA.117.311082.
8
Muscle volume loss as a prognostic marker in hepatocellular carcinoma patients treated with sorafenib.
Hepatol Res. 2017 May;47(6):558-565. doi: 10.1111/hepr.12780. Epub 2016 Aug 30.
9
Cause and management of muscle wasting in chronic liver disease.
Curr Opin Gastroenterol. 2016 May;32(3):159-65. doi: 10.1097/MOG.0000000000000261.
10
Review article: sarcopenia in cirrhosis--aetiology, implications and potential therapeutic interventions.
Aliment Pharmacol Ther. 2016 Apr;43(7):765-77. doi: 10.1111/apt.13549. Epub 2016 Feb 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验