Sarcopenia as a predictor of post-transplant tumor recurrence after living donor liver transplantation for hepatocellular carcinoma beyond the Milan criteria

被引:29
|
作者
Kim, Young Ri [1 ]
Park, Sukhee [1 ]
Han, Sangbin [1 ]
Ahn, Joong Hyun [2 ]
Kim, Seonwoo [2 ]
Sinn, Dong Hyun [3 ]
Jeong, Woo Kyoung [4 ]
Ko, Justin S. [1 ]
Gwak, Mi Sook [1 ]
Kim, Gaab Soo [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Anesthesiol & Pain Med, Seoul 06351, South Korea
[2] Samsung Med Ctr, Stati & Data Ctr, Seoul 06351, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med, Seoul 06351, South Korea
[4] Sungkyunkwan Univ, Sch Med, Dept Radiol, Seoul 06351, South Korea
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
COMPUTED-TOMOGRAPHY; SKELETAL-MUSCLE; CIRRHOSIS; SURVIVAL; OBESITY; MODEL; DIAGNOSIS; ATROPHY; RISK;
D O I
10.1038/s41598-018-25628-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To evaluate the association between sarcopenia and tumor recurrence after living donor liver transplantation (LDLT) in patients with advanced hepatocellular carcinoma (HCC), we analyzed 92 males who underwent LDLT for treating HCC beyond the Milan criteria. Sarcopenia was defined when the height-normalized psoas muscle thickness was < 15.5 mm/m at the L3 vertebra level on computed tomography based on an optimum stratification method using the Gray's test statistic. Survival analysis was performed with death as a competing risk event. The primary outcome was post-transplant HCC recurrence. The median follow-up time was 36 months. There was a 9% increase in recurrence risk per unit decrease in height-normalized psoas muscle thickness. Twenty-six (36.1%) of 72 sarcopenic recipients developed HCC recurrence, whereas only one (5.0%) of 20 non-sarcopenic recipients developed HCC recurrence. Recurrence risk was greater in sarcopenic patients in univariable analysis (hazard ratio [HR] = 8.06 [1.06-16.70], p = 0.044) and in multivariable analysis (HR = 9.49 [1.18-76.32], p = 0.034). Greater alpha-fetoprotein and microvascular invasion were also identified as independent risk factors. Incorporation of sarcopenia improved the model fitness and prediction power of the estimation model. In conclusion, sarcopenia appears to be one of the important host factors modulating tumor recurrence risk after LDLT for advanced HCC.
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页数:11
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