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
Department of Gastroenterology and Metabolism, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Liver Cancer. 2020 Apr;9(2):148-155. doi: 10.1159/000503829. Epub 2019 Nov 8.
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.
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.
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).
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.
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。
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。
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。
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。