Department of Medical Oncology, Institute of Oncology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
Department of Internal Medicine and Medical Oncology, Research and Practice Hospital, Balıkesir University, Balıkesir, Turkey.
J Oncol Pharm Pract. 2021 Sep;27(6):1357-1363. doi: 10.1177/1078155220959427. Epub 2020 Sep 22.
The efficacy and tolerability of modern cytotoxic chemotherapy regimens used in malnourished metastatic colorectal cancer (mCRC) patients is uncertain. The aim of this study was to investigate the effect of malnutrition on efficacy and tolerability of cytotoxic chemotherapy and overall survival in mCRC patients.
In this multicenter study, demographic, oncologic and nutritional data were collected prospectively from mCRC patients. Nutritional status of the patients were evaluated on the basis of NRI (Nutritional Risk Assessment), BMI (Body Mass Index) and WL (Weight Loss) before the first chemotherapy, after the first and second chemotherapy during 2 cycles of chemotherapy every 15 days. To determine the inter-treatment weight loss toxicity assessment was included to theese parameters after each chemotherapy. NRI calculation was performed as [1.51xserum albumin level (g/L)+41.7xcurrent weight/basic weight]. NRIs were examined in 3 categories as 'no malnutrition' (NRI >97.5), 'moderate malnutrition' (97.5 ≥NRI ≥83.5) or 'severe malnutrition' (NRI <83.5). Response to treatment and drug-induced toxicities were assessed based on Criteria in Solid Tumors (RECIST) 1.1 and National Cancer Institute CTCAE version 4.0 respectively.
One-hundred and thirty-seven mCRC patients were prospectively included. Median age was 48 (range 18-83). Primary location was colon in 66% of patients and 84% of their primary source was left colon. Malnutrition was detected in 39% of the cases. Response rate to treatment was twenty four percent. While there was no significant relationship between chemotherapy response and moderate/severe malnutrition (p = 0.24), moderate/severe malnutrition was associated with multipl site of metastases, WHO PS (World Health Organization Performance Status) of 1, over the median value of CEA/CA 19-9 (carcinoembryonic antigen/carbohydate antigen 19-9) levels (p = 0.003, p = 0.03, p < 0.001, and p = 0.02; respectively). Hypoalbuminemia and moderate/severe malnutrition were associated with all types of toxicity (p < 0.001 and p < 0.001). Moderate/severe malnutrition was associated with thrombocytopenia, and diarrhea following chemotherapy predominately, (p = 0.02 and p = 0.04; respectively). In moderate/severe malnutrition group median overall survival was prominently shorter than those with no malnutrition [6.6 moths (95%CI, 5.6-7.6) vs 11.9 moths (95% CI, 11.1-12.7) respectively, p < 0.001].
Our study showed that moderate/severe malnutrition in mCRC patients was associated with decreased overall survival and increased chemotherapy toxicity.
在营养不良的转移性结直肠癌(mCRC)患者中,现代细胞毒性化疗方案的疗效和耐受性尚不确定。本研究旨在探讨营养不良对 mCRC 患者细胞毒性化疗的疗效和耐受性以及总生存期的影响。
在这项多中心研究中,前瞻性收集了 mCRC 患者的人口统计学、肿瘤学和营养数据。在每 15 天进行 2 个周期的化疗期间,在第一次化疗前、第一次化疗后和第二次化疗后,根据 NRI(营养风险评估)、BMI(体重指数)和 WL(体重减轻)评估患者的营养状况。为了确定治疗期间的体重减轻毒性评估,在每次化疗后将其纳入这些参数。NRI 计算方法为[1.51x血清白蛋白水平(g/L)+41.7x当前体重/基础体重]。NRI 分为 3 类:“无营养不良”(NRI>97.5)、“中度营养不良”(97.5≥NRI≥83.5)或“重度营养不良”(NRI<83.5)。根据实体瘤反应评估标准(RECIST)1.1 和国家癌症研究所 CTCAE 版本 4.0 评估治疗反应和药物引起的毒性。
前瞻性纳入了 137 名 mCRC 患者。中位年龄为 48 岁(范围 18-83 岁)。原发部位在结肠的占 66%,原发部位在左结肠的占 84%。39%的病例存在营养不良。治疗反应率为 24%。虽然中度/重度营养不良与化疗反应无显著关系(p=0.24),但中度/重度营养不良与多部位转移、WHO PS(世界卫生组织表现状态)为 1、CEA/CA 19-9(癌胚抗原/碳水化合物抗原 19-9)水平超过中位数有关(p=0.003、p=0.03、p<0.001 和 p=0.02)。低白蛋白血症和中度/重度营养不良与所有类型的毒性相关(p<0.001 和 p<0.001)。中度/重度营养不良与化疗后血小板减少症和腹泻相关(p=0.02 和 p=0.04)。在中度/重度营养不良组,中位总生存期明显短于无营养不良组[6.6 个月(95%CI,5.6-7.6)与 11.9 个月(95%CI,11.1-12.7)相比,p<0.001]。
本研究表明,mCRC 患者的中度/重度营养不良与总生存期缩短和化疗毒性增加有关。