Department of Pediatric Surgery, Reproductive and Developmental Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Pediatric Surgery, Reproductive and Developmental Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Surg Res. 2019 Apr;236:101-105. doi: 10.1016/j.jss.2018.10.048. Epub 2018 Dec 7.
Sarcopenia is a syndrome that is defined by the loss of skeletal muscle mass, quality, and strength. In adult patients with malignancies, the presence of sarcopenia is known to be correlated with a poor prognosis; however, there have been no reports on the influence of sarcopenia on malignant tumors in pediatric patients. In the present study, we investigated whether or not sarcopenia affects the prognosis of high-risk neuroblastoma.
Thirteen patients with high-risk neuroblastoma who were treated according to the standard protocol at our hospital from 2007 to 2016 were divided into a progression-free survival group (n = 8) and a relapse/death group (n = 5). The rate of change in sarcopenia was calculated by comparing the psoas muscle area (PMA) of the L3-level lumbar spine on computed tomography before and after treatment with the standard protocol. The rate of change in the PMA, Kaup index, and serum albumin level were compared. Furthermore, we determined the cutoff rate of change in the PMA and compared the overall and progression-free survival.
The rates of change in the PMA were 1.24 and 0.84 in the progression-free survival and relapse/death groups, respectively (P = 0.0472). There were no significant differences in the rates of change in the Kaup index or the serum albumin level of the two groups. The patients whose rate of change in the PMA was >1.00 showed a prolonged overall (P = 0.0078) and progression-free survival (P = 0.006).
A decrease in the skeletal muscle mass was suggested to be a significant prognostic factor for high-risk neuroblastoma.
肌肉减少症是一种以骨骼肌质量、质量和力量丧失为特征的综合征。在患有恶性肿瘤的成年患者中,已知存在肌肉减少症与预后不良相关;然而,尚未有关于肌肉减少症对儿科患者恶性肿瘤的影响的报告。在本研究中,我们研究了肌肉减少症是否影响高危神经母细胞瘤的预后。
将我院 2007 年至 2016 年按照标准方案治疗的 13 例高危神经母细胞瘤患者分为无进展生存组(n=8)和复发/死亡组(n=5)。通过比较治疗前后标准方案的 L3 腰椎水平的腰大肌面积(PMA)来计算肌肉减少症的变化率。比较 PMA、Kaup 指数和血清白蛋白水平的变化率。此外,我们确定了 PMA 变化率的截止值,并比较了总生存和无进展生存。
无进展生存组和复发/死亡组的 PMA 变化率分别为 1.24 和 0.84(P=0.0472)。两组的 Kaup 指数或血清白蛋白水平变化率无显著差异。PMA 变化率>1.00 的患者总生存(P=0.0078)和无进展生存(P=0.006)延长。
骨骼肌质量的减少被认为是高危神经母细胞瘤的一个重要预后因素。