Duke University School of Medicine, Duke University Medical Center, Durham, NC, U.S.A.
Duke Cancer Institute, Duke University Medical Center, Durham, NC, U.S.A.
Anticancer Res. 2020 Sep;40(9):5245-5254. doi: 10.21873/anticanres.14528.
BACKGROUND/AIM: To determine whether BMI and sarcopenia were related to treatment-limiting toxicity or efficacy of pembrolizumab treatment in melanoma patients.
Medical records for melanoma patients undergoing pembrolizumab treatment at Duke University from January 2014 to September 2018 were reviewed. Pre-treatment measurements such as BMI were collected. Pre-treatment CT imaging was used to determine psoas muscle index (PMI). Patients in the lowest sex-specific tertile of PMI were sarcopenic. Logistic regression measured associations with treatment toxicity and response. Kaplan-Meier analysis assessed progression-free survival (PFS) and overall survival (OS).
Among 156 patients, the overall objective response rate was 46.2% and 29 patients (18.6%) experienced treatment-limiting toxicity. Sarcopenia was not significantly associated with toxicity, response, or survival. However, obese patients (BMI >30) experienced higher rates of toxicity (p=0.0007).
Sarcopenia did not appear to predict clinically relevant outcomes. Obesity, however, represents a readily available predictor of pembrolizumab toxicity.
背景/目的:确定 BMI 和肌肉减少症是否与黑色素瘤患者接受 pembrolizumab 治疗的治疗限制毒性或疗效相关。
回顾了 2014 年 1 月至 2018 年 9 月期间在杜克大学接受 pembrolizumab 治疗的黑色素瘤患者的病历。收集了 BMI 等治疗前测量值。使用治疗前 CT 成像来确定竖脊肌指数 (PMI)。PMI 处于性别特异性最低三分位的患者患有肌肉减少症。Logistic 回归分析了与治疗毒性和反应的相关性。Kaplan-Meier 分析评估了无进展生存期 (PFS) 和总生存期 (OS)。
在 156 名患者中,总体客观缓解率为 46.2%,29 名患者 (18.6%) 出现治疗限制毒性。肌肉减少症与毒性、反应或生存无显著相关性。然而,肥胖患者 (BMI >30) 毒性发生率更高 (p=0.0007)。
肌肉减少症似乎不能预测临床相关结局。然而,肥胖是 pembrolizumab 毒性的一个易于识别的预测因素。