TY - JOUR
T1 - Skeletal muscle status and survival among patients with advanced biliary tract cancer
AU - Takaoka, Shinya
AU - Hamada, Tsuyoshi
AU - Takahara, Naminatsu
AU - Saito, Kei
AU - Endo, Go
AU - Hakuta, Ryunosuke
AU - Ishida, Kota
AU - Ishigaki, Kazunaga
AU - Kanai, Sachiko
AU - Kurihara, Kohei
AU - Oyama, Hiroki
AU - Saito, Tomotaka
AU - Sato, Tatsuya
AU - Suzuki, Tatsunori
AU - Suzuki, Yukari
AU - Tange, Shuichi
AU - Tokito, Yurie
AU - Tateishi, Ryosuke
AU - Nakai, Yousuke
AU - Fujishiro, Mitsuhiro
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/3
Y1 - 2024/3
N2 - Background: Studies have demonstrated a prognostic role of sarcopenia (i.e., loss of skeletal muscle volume and functionality) in patients with various cancer types. In patients with biliary tract cancer, the quantity and quality of skeletal muscles and their serial changes have not been fully investigated in relation to survival outcomes. Methods: We identified 386 patients with unresectable or recurrent biliary tract cancer and calculated skeletal muscle index (SMI) and skeletal muscle density (SMD) to estimate muscular quantity and quality, respectively, based on computed tomography images. Using the Cox regression model with adjustment for potential confounders, we calculated hazard ratios (HRs) and 95% confidence intervals (CIs) for progression-free survival (PFS) and overall survival (OS) according to skeletal muscle status and its serial change. Results: Compared to patients without sarcopenia, patients with sarcopenia were associated with shorter PFS (multivariable HR, 1.60; 95% CI, 1.15–2.22; P = 0.005), but not with OS (P = 0.027) at the adjusted α level of 0.013. SMD at baseline was associated with OS (multivariable HR comparing the extreme quartiles, 1.52; 95% CI, 1.07–2.14; Ptrend = 0.012), but not with PFS (Ptrend = 0.13). A reduction in SMI rather than that in SMD was associated with OS. Progressive disease was a risk factor for reductions in SMI and SMD. Conclusions: Skeletal muscle quantity and quality and their serial changes were associated with survival outcomes in patients with advanced biliary tract cancer. Our data highlight the importance of designing nutritional and physical interventions for improvements in skeletal muscle status.
AB - Background: Studies have demonstrated a prognostic role of sarcopenia (i.e., loss of skeletal muscle volume and functionality) in patients with various cancer types. In patients with biliary tract cancer, the quantity and quality of skeletal muscles and their serial changes have not been fully investigated in relation to survival outcomes. Methods: We identified 386 patients with unresectable or recurrent biliary tract cancer and calculated skeletal muscle index (SMI) and skeletal muscle density (SMD) to estimate muscular quantity and quality, respectively, based on computed tomography images. Using the Cox regression model with adjustment for potential confounders, we calculated hazard ratios (HRs) and 95% confidence intervals (CIs) for progression-free survival (PFS) and overall survival (OS) according to skeletal muscle status and its serial change. Results: Compared to patients without sarcopenia, patients with sarcopenia were associated with shorter PFS (multivariable HR, 1.60; 95% CI, 1.15–2.22; P = 0.005), but not with OS (P = 0.027) at the adjusted α level of 0.013. SMD at baseline was associated with OS (multivariable HR comparing the extreme quartiles, 1.52; 95% CI, 1.07–2.14; Ptrend = 0.012), but not with PFS (Ptrend = 0.13). A reduction in SMI rather than that in SMD was associated with OS. Progressive disease was a risk factor for reductions in SMI and SMD. Conclusions: Skeletal muscle quantity and quality and their serial changes were associated with survival outcomes in patients with advanced biliary tract cancer. Our data highlight the importance of designing nutritional and physical interventions for improvements in skeletal muscle status.
KW - Body composition
KW - Chemotherapy
KW - Cholangiocarcinoma
KW - Cohort studies
KW - Sarcopenia
KW - Survival analysis
UR - http://www.scopus.com/inward/record.url?scp=85184173602&partnerID=8YFLogxK
U2 - 10.1007/s10147-023-02466-z
DO - 10.1007/s10147-023-02466-z
M3 - Article
C2 - 38319509
AN - SCOPUS:85184173602
SN - 1341-9625
VL - 29
SP - 297
EP - 308
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 3
ER -