Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Radiology Department, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Curr Oncol. 2021 Mar 23;28(2):1325-1337. doi: 10.3390/curroncol28020126.
Our study measured the body composition of Diffuse large B-cell lymphoma (DLBCL) patients receiving rituximab with cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) regimen by computed tomographic (CT) and assessed their correlation with treatment-related toxicity and other adverse outcomes.
We retrospectively analyzed 201 DLBCL patients who underwent pre-treatment abdominal CT examination. CT images were used to assess body composition metrics at the third lumbar vertebrae including fat tissues and muscle. Based on the skeletal muscle area (SMA) and density (SMD), skeletal muscle index (SMI), skeletal muscle gauge (SMG = SMI × SMD) and lean body mass (LBM) were calculated. Also analyzed were the toxicity, adverse events and survival.
We found that SMG, SMD, SMI and LBM were correlated with any grade 3-4 toxicity, dose reduction, hospitalization or termination of the treatment due to immunochemotherapy and worse survival. However, multivariate analysis demonstrated SMG [progression-free survival (PFS): hazard ratio (HR), 2.889; 95% CI, 1.401-5.959; = 0.004; overall survival (OS): HR, 2.655; 95% CI, 1.218-5.787; = 0.014] was the best predictor of poor prognosis.
SMG, SMD, SMI and LBM were identified as predictors of adverse reactions and poor survival. SMG was an innovative and valuable indicator of immunochemotherapy toxicity and other adverse outcomes. Additionally, it can be used to individualize antineoplastic drug dosing.
本研究通过计算机断层扫描(CT)测量接受利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)方案治疗的弥漫性大 B 细胞淋巴瘤(DLBCL)患者的身体成分,并评估其与治疗相关毒性和其他不良结局的相关性。
我们回顾性分析了 201 例接受治疗前腹部 CT 检查的 DLBCL 患者。使用 CT 图像评估第三腰椎处的身体成分指标,包括脂肪组织和肌肉。基于骨骼肌面积(SMA)和密度(SMD),计算骨骼肌指数(SMI)、骨骼肌测量仪(SMG = SMI × SMD)和瘦体重(LBM)。还分析了毒性、不良事件和生存情况。
我们发现 SMG、SMD、SMI 和 LBM 与任何 3-4 级毒性、剂量减少、因免疫化疗而住院或终止治疗以及更差的生存相关。然而,多变量分析表明 SMG [无进展生存期(PFS):风险比(HR),2.889;95%置信区间,1.401-5.959; = 0.004;总生存期(OS):HR,2.655;95%置信区间,1.218-5.787; = 0.014]是预后不良的最佳预测因子。
SMG、SMD、SMI 和 LBM 是预测不良反应和不良生存的指标。SMG 是免疫化疗毒性和其他不良结局的创新性和有价值的指标。此外,它可以用于个体化抗肿瘤药物剂量。