Department of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Harvard Medical School, Boston, MA, USA.
J Immunother Cancer. 2019 Mar 29;7(1):89. doi: 10.1186/s40425-019-0512-5.
A male gender driven obesity paradox (improved survival for overweight/obese patients compared to normal weight) was recently shown in melanoma in the context of checkpoint inhibition (anti-PD-1/anti-CTLA4 monotherapy) in a pooled meta-analysis. We characterized the relationship of Body Mass Index (BMI) with survival and explored gender-based interactions with surrogates of body composition/malnutrition in the context of PD-1 blockade as monotherapy or in combination with ipilimumab in a real-world setting.
Advanced melanoma patients who received at least one dose of pembrolizumab, nivolumab, or nivolumab plus ipilimumab (combination) from June 2014 to September 2016 were included in this retrospective cohort study (N = 139). Overall Survival (OS) and Progression Free Survival (PFS) were the main outcomes. Analysis was performed using Random Survival Forests (RSF)/ multivariable Cox Proportional-Hazards models.
Overweight/Class-I (25- < 35 kg/m) obese patients had a significantly lower risk of mortality (adjusted-HR:0.26; 95%CI:0.1-0.71; p-value = 0.008) and progressive disease (adjusted-HR:0.43; 95%CI:0.19-0.95; p-value:0.038) compared to normal-weight (18.5- < 25 kg/m). Class II/III obesity (compared to normal-weight) had an adjusted HR of 0.42 (95%CI: 0.1-1.77; p-value: 0.238) for OS and 1 (95%CI:0.34-2.94; p-value:0.991) for PFS. Exploration of interactions for OS showed that the association was predominantly driven by males (adjusted-HR:0.11; 95%CI:0.03-0.4; adjusted-HR: 0.56; 95%CI:0.16-1.89 p-value:0.044); the association was not seen in patients with serum creatinine< 0.9 mg/dL (adjusted-HR:0.43; 95%CI:0.15-1.24; p-value:0.020), who were predominantly females. These observations were made in both the anti-PD-1 monotherapy (n = 79) and combination therapy (anti-PD-1/CTLA-4, n = 60) cohorts.
The findings support the existence of an "obesity paradox" restricted to overweight/Class-I obesity in the real-world setting; the association was driven predominantly by males who largely had higher serum creatinine levels, a surrogate for skeletal muscle mass in the setting of metastatic disease. These observations suggest that sarcopenia (low skeletal muscle mass) or direct measures of body mass composition may be more suitable predictors of survival in melanoma patients treated with PD-1 blockade (monotherapy/combination).
最近在黑色素瘤中进行的一项汇集荟萃分析显示,男性性别驱动的肥胖悖论(超重/肥胖患者的生存改善与正常体重患者相比)在检查点抑制(抗 PD-1/抗 CTLA-4 单药治疗)的情况下存在。我们描述了体重指数(BMI)与生存的关系,并在真实世界环境中探索了 PD-1 阻断作为单药治疗或与 ipilimumab 联合治疗时,性别与身体成分/营养不良的替代指标之间的相互作用。
本回顾性队列研究纳入了 2014 年 6 月至 2016 年 9 月期间至少接受过 pembrolizumab、nivolumab 或 nivolumab 联合 ipilimumab(联合治疗)的晚期黑色素瘤患者(N=139)。总生存(OS)和无进展生存(PFS)是主要终点。使用随机生存森林(RSF)/多变量 Cox 比例风险模型进行分析。
超重/1 级肥胖(25-<35kg/m)患者的死亡率(调整后 HR:0.26;95%CI:0.1-0.71;p 值=0.008)和进展性疾病(调整后 HR:0.43;95%CI:0.19-0.95;p 值:0.038)的风险显著降低。2 级/3 级肥胖(与正常体重相比)的 OS 调整后 HR 为 0.42(95%CI:0.1-1.77;p 值:0.238),PFS 调整后 HR 为 1(95%CI:0.34-2.94;p 值:0.991)。对 OS 的交互作用的探索表明,这种关联主要由男性驱动(调整后 HR:0.11;95%CI:0.03-0.4;调整后 HR:0.56;95%CI:0.16-1.89;p 值:0.044);在血清肌酐<0.9mg/dL(调整后 HR:0.43;95%CI:0.15-1.24;p 值:0.020)的患者中未观察到这种关联,这些患者主要为女性。这些观察结果在抗 PD-1 单药治疗(n=79)和联合治疗(抗 PD-1/CTLA-4,n=60)队列中均可见。
这些发现支持在真实世界环境中存在“肥胖悖论”,仅限于超重/1 级肥胖;这种关联主要由男性驱动,这些男性的血清肌酐水平较高,这是转移性疾病中骨骼肌质量的替代指标。这些观察结果表明,在接受 PD-1 阻断(单药治疗/联合治疗)治疗的黑色素瘤患者中,肌肉减少症(低骨骼肌质量)或身体成分的直接测量可能是更合适的生存预测指标。