Meyer Hans-Jonas, Strobel Alexandra, Wienke Andreas, Surov Alexey
Department of Diagnostic and Interventional Radiology, University of Leipzig, Leipzig, Germany.
Institute of Medical Epidemiology, Biostatistics, and Informatics, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany; Profile Area Clinical Studies and Biostatistics, Halle (Saale), Germany.
Clin Colorectal Cancer. 2022 Sep;21(3):e213-e225. doi: 10.1016/j.clcc.2022.03.005. Epub 2022 Jun 3.
Low-skeletal muscle mass (LSMM) is defined as skeletal muscle loss, which can be assessed by imaging. Our aim was to establish the effect of LSMM on overall survival (OS) in metastasized colorectal cancer patients based on a large patient sample.
MEDLINE library, EMBASE, and SCOPUS databases were screened for the associations between LSMM and mortality in metastasized colorectal cancer patients up to March 2022. The primary aim of the systematic review was to investigate the influence of LSMM on overall survival (OS) by means of the effect of measure hazard ratio. Fifteen studies were included into the present analysis.
The included studies comprised 1744 patients. The frequency of LSMM was 46.2%. Associations between LSMM and OS were as follows: hazard ratio (HR) = 1.34 (95% confidence interval [CI] 0.94-1.91), P = .10 in univariable analysis and HR = 2.05 (95% CI 1.18-3.56), P = .01 in multivariable analysis. LSMM influenced OS in patients undergoing first-line chemotherapy, HR = 1.51 (95% CI 1.20-1.89), P = .0004. In patients undergoing second- and third-line chemotherapy, LSMM was not associated with OS, HR = 1.43 (95% CI 0.65-3.14), P = .37 Also, LSMM did not affect OS in patients with resection of hepatic metastases, HR = 0.93 (95% CI 0.70-1.24), P = .63. LSMM tended to affect progression-free survival, HR = 1.49 (95% CI 0.94-2.35), P = .09. LSMM did not predict treatment toxicity, odds ratio (OR) = 1.52 (95% CI 0.84-2.72), P = .16.
LSMM occurs in 46.2% of patients with metastasized colorectal cancers. LSMM is associated with OS in patients undergoing first-line chemotherapy. LSMM does not affect OS in second- and third-line chemotherapy and in patients undergoing resection of hepatic metastases. LSMM is not associated with progression-free survival and treatment toxicity.
低骨骼肌质量(LSMM)被定义为骨骼肌流失,可通过影像学评估。我们的目的是基于大量患者样本,确定LSMM对转移性结直肠癌患者总生存期(OS)的影响。
检索MEDLINE数据库、EMBASE数据库和SCOPUS数据库,以查找截至2022年3月的转移性结直肠癌患者中LSMM与死亡率之间的关联。本系统评价的主要目的是通过测量风险比的效应来研究LSMM对总生存期(OS)的影响。本分析纳入了15项研究。
纳入的研究共1744例患者。LSMM的发生率为46.2%。LSMM与OS之间的关联如下:单因素分析中,风险比(HR)=1.34(95%置信区间[CI]0.94 - 1.91),P = 0.10;多因素分析中,HR = 2.05(95%CI 1.18 - 3.56),P = 0.01。LSMM对接受一线化疗患者的OS有影响,HR = 1.51(95%CI 1.20 - 1.89),P = 0.0004。在接受二线和三线化疗的患者中,LSMM与OS无关,HR = 1.43(95%CI 0.65 - 3.14),P = 0.37。此外,LSMM对肝转移切除患者的OS无影响,HR = 0.93(95%CI 0.70 - 1.24),P = 0.63。LSMM倾向于影响无进展生存期,HR = 1.49(95%CI 0.94 - 2.35),P = 0.09。LSMM不能预测治疗毒性,比值比(OR) = 1.52(95%CI 0.84 - 2.72),P = 0.16。
46.2%的转移性结直肠癌患者存在LSMM。LSMM与接受一线化疗患者的OS相关。LSMM对二线和三线化疗患者以及肝转移切除患者的OS无影响。LSMM与无进展生存期和治疗毒性无关。