Lee Ji Hyun, Jee Byul A, Kim Jae-Hun, Bae Hoyoung, Chung Jae Hoon, Song Wan, Sung Hyun Hwan, Jeon Hwang Gyun, Jeong Byong Chang, Seo Seong Il, Jeon Seong Soo, Lee Hyun Moo, Park Se Hoon, Kang Minyong
Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Cancers (Basel). 2021 Dec 17;13(24):6345. doi: 10.3390/cancers13246345.
The clinical value of sarcopenia has not been determined yet in metastatic hormone-sensitive prostate cancer (mHSPC). We retrospectively evaluated data of 70 consecutive patients with mHSPC receiving treatment with either early docetaxel ( = 42) or abiraterone acetate ( = 28) between July 2018 and April 2021. Skeletal muscle index was calculated from cross-sectional areas of skeletal muscle on baseline computed tomography (CT), defining sarcopenia as a skeletal muscle index of ≤52.4 cm/m. Failure-free survival (FFS), radiographic progression-free survival, and time to prostate-specific antigen (PSA) progression were estimated using the Kaplan-Meier method, and differences in survival probability were compared using the log-rank test. Cox proportional hazards regression analysis was conducted to identify the predictors of clinical outcomes. Patients with sarcopenia ( = 47) had shorter FFS than those without sarcopenia ( = 23) (median, 20.1 months vs. not reached; log-rank < 0.001). Sarcopenia was independently associated with shorter FFS (hazard ratio (HR), 6.69; 95% confidence interval (CI), 1.57-28.49; = 0.010) and time to PSA progression (HR, 12.91; 95% CI, 1.08-153.85; = 0.043). In conclusion, sarcopenia is an independent prognostic factor for poor FFS and time to PSA progression in patients with mHSPC who receive early docetaxel or abiraterone acetate treatment.
肌肉减少症在转移性激素敏感性前列腺癌(mHSPC)中的临床价值尚未确定。我们回顾性评估了2018年7月至2021年4月期间连续70例接受早期多西他赛(n = 42)或醋酸阿比特龙(n = 28)治疗的mHSPC患者的数据。根据基线计算机断层扫描(CT)上的骨骼肌横截面积计算骨骼肌指数,将肌肉减少症定义为骨骼肌指数≤52.4 cm²/m²。采用Kaplan-Meier方法估计无失败生存期(FFS)、影像学无进展生存期和前列腺特异性抗原(PSA)进展时间,并使用对数秩检验比较生存概率差异。进行Cox比例风险回归分析以确定临床结局的预测因素。有肌肉减少症的患者(n = 47)的FFS比无肌肉减少症的患者(n = 23)短(中位数,20.1个月对未达到;对数秩P < 0.001)。肌肉减少症与较短的FFS(风险比(HR),6.69;95%置信区间(CI),1.57 - 28.49;P = 0.010)和PSA进展时间(HR,12.91;95%CI,1.08 - 153.85;P = 0.043)独立相关。总之,对于接受早期多西他赛或醋酸阿比特龙治疗的mHSPC患者,肌肉减少症是FFS不佳和PSA进展时间的独立预后因素。