Pennington Biomedical Research Center, Baton Rouge, LA, USA; LSU Health Sciences Center New Orleans School of Medicine, New Orleans, LA, USA; Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Dana-Farber Cancer Institute, Boston MA, USA.
Clin Nutr. 2022 Jul;41(7):1600-1604. doi: 10.1016/j.clnu.2022.05.016. Epub 2022 May 27.
BACKGROUND & AIMS: Patients with colon cancer who prematurely discontinue postoperative chemotherapy may have an increased risk of disease recurrence and death. This study tested the hypothesis that the quantity and distribution of abdominal adipose tissue predict premature chemotherapy discontinuation.
This cohort study included 533 patients with stage II-III colon cancer who initiated a planned regimen of 24-weeks of 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) chemotherapy. The primary exposures were body mass index (BMI) and computed tomography-derived abdominal adiposity measures (e.g., visceral, subcutaneous, and intramuscular adipose tissue). The primary endpoint was premature chemotherapy discontinuation, defined as receiving <6 cycles of FOLFOX. Generalized linear models quantified the relative risk (RR) of premature chemotherapy discontinuation adjusted for age, sex, cancer stage, height, and muscle area, using two-sided statistical tests.
Forty-two patients [7.9% (95% CI: 5.7, 10.5)] prematurely discontinued chemotherapy. Visceral adipose tissue [RR: 3.27 (95% CI: 1.26, 8.49)] and intramuscular adipose tissue [RR: 2.79 (95% CI: 1.09, 7.12)] were statistically significantly associated with an increased risk of premature chemotherapy discontinuation. BMI [RR: 2.07 (95% CI: 0.75, 5.73)] and subcutaneous adipose tissue [RR: 2.32 (95% CI: 0.91, 5.94)] were not statistically significantly associated with premature chemotherapy discontinuation.
Among patients with stage II-III colon cancer who initiate postoperative chemotherapy, excess visceral and intramuscular adiposity may be risk factors for the premature discontinuation of chemotherapy.
提前停止术后化疗的结肠癌患者疾病复发和死亡的风险可能会增加。本研究检验了这样一个假设,即腹部脂肪组织的数量和分布可预测提前停止化疗。
本队列研究纳入了 533 例接受计划 24 周氟尿嘧啶、亚叶酸钙和奥沙利铂(FOLFOX)化疗的 II-III 期结肠癌患者。主要暴露因素为体重指数(BMI)和计算机断层扫描(CT)检测到的腹部肥胖测量值(如内脏、皮下和肌肉内脂肪组织)。主要终点为提前停止化疗,定义为接受 <6 个周期的 FOLFOX。使用双侧统计检验,广义线性模型调整年龄、性别、癌症分期、身高和肌肉面积后,量化了提前停止化疗的相对风险(RR)。
42 例患者(7.9%(95%CI:5.7,10.5))提前停止化疗。内脏脂肪组织(RR:3.27(95%CI:1.26,8.49))和肌肉内脂肪组织(RR:2.79(95%CI:1.09,7.12))与提前停止化疗的风险增加具有统计学显著相关性。BMI(RR:2.07(95%CI:0.75,5.73))和皮下脂肪组织(RR:2.32(95%CI:0.91,5.94))与提前停止化疗无统计学显著相关性。
在接受术后化疗的 II-III 期结肠癌患者中,过多的内脏和肌肉内脂肪可能是提前停止化疗的危险因素。