Correlation of reduced temporal muscle thickness and systemic muscle loss in newly diagnosed glioblastoma patients

被引:14
|
作者
Ten Cate, Cecil [1 ]
Huijs, Sandra M. H. [2 ]
Willemsen, Anna C. H. [3 ,4 ,5 ]
Pasmans, Raphael C. O. S. [2 ]
Eekers, Danielle B. P. [6 ]
Zegers, Catharina M. L. [6 ]
Ackermans, Linda [7 ]
Beckervordersandforth, Jan [3 ,8 ]
van Raak, Elisabeth P. M. [9 ]
Anten, Monique H. M. E. [3 ,9 ]
Hoeben, Ann [3 ,5 ]
Postma, Alida A. [10 ]
Broen, Martinus P. G. [3 ,9 ]
机构
[1] Maastricht Univ, Master Sci Med & Clin Res, Maastricht, Netherlands
[2] Zuyderland Med Ctr, Dept Neurol, Heerlen, Netherlands
[3] Maastricht Univ, GROW Sch Oncol & Reprod, Maastricht, Netherlands
[4] Maastricht Univ, NUTRIM Sch Nutr & Translat Res Metab, Dept Resp Med, Med Ctr, Maastricht, Netherlands
[5] Maastricht Univ, Dept Internal Med, Div Med Oncol, Med Ctr, Maastricht, Netherlands
[6] Maastricht Univ, GROW Sch Oncol & Reprod, Dept Radiat Oncol Maastro, Med Ctr, Maastricht, Netherlands
[7] Maastricht Univ, Dept Neurosurg, Med Ctr, Maastricht, Netherlands
[8] Maastricht Univ, Dept Pathol, Med Ctr, Maastricht, Netherlands
[9] Maastricht Univ, Dept Neurol, Med Ctr, POB 5800, NL-6202 AZ Maastricht, Netherlands
[10] Maastricht Univ, Dept Radiol, Med Ctr, Maastricht, Netherlands
关键词
Temporal muscle thickness; Skeletal muscle area; Glioblastoma; Sarcopenia; Imaging marker; SKELETAL-MUSCLE; SARCOPENIA; CANCER;
D O I
10.1007/s11060-022-04180-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Reduced temporal muscle thickness (TMT) has recently been postulated as a prognostic imaging marker and an objective tool to assess patients frailty in glioblastoma. Our aim is to investigate the correlation of TMT and systemic muscle loss to confirm that TMT is an adequate surrogate marker of sarcopenia in newly diagnosed glioblastoma patients. Methods TMT was assessed on preoperative MR-images and skeletal muscle area (SMA) was assessed at the third lumbar vertebra on preoperative abdominal CT-scans. Previous published TMT sex-specific cut-off values were used to classify patients as 'patient at risk of sarcopenia' or 'patient with normal muscle status'. Correlation between TMT and SMA was assessed using Spearman's rank correlation coefficient. Results Sixteen percent of the 245 included patients were identified as at risk of sarcopenia. The mean SMA of glioblastoma patients at risk of sarcopenia (124.3 cm(2), SD 30.8 cm(2)) was significantly lower than the mean SMA of patients with normal muscle status (146.3 cm(2), SD 31.1 cm(2), P < .001). We found a moderate association between TMT and SMA in the patients with normal muscle status (Spearman's rho 0.521, P < .001), and a strong association in the patients at risk of sarcopenia (Spearman's rho 0.678, P < .001). Conclusion Our results confirm the use of TMT as a surrogate marker of total body skeletal muscle mass in glioblastoma, especially in frail patients at risk of sarcopenia. TMT can be used to identify patients with muscle loss early in the disease process, which enables the implementation of adequate intervention strategies.
引用
收藏
页码:611 / 618
页数:8
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