Department of Medical Oncology, Università Politecnica delle Marche, AOU delle Marche, Ancona, Italy.
Department of Pulmonary Medicine, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Oncologist. 2024 Mar 4;29(3):e372-e381. doi: 10.1093/oncolo/oyad273.
Specific components of lipid profile seem to differently impact on immune activity against cancer and unraveling their prognostic role in patients with solid cancer treated with immune checkpoint inhibitors (ICIs) is needed.
We retrospectively collected baseline clinicopathological characteristics including circulating lipid profile (total cholesterol [TC], triglycerides [TG], low-density lipoproteins [LDL], high-density lipoproteins [HDL]) of patients with consecutive solid cancer treated with ICIs, and we investigated their role in predicting clinical outcomes.
At a median follow-up of 32.9 months, among 430 enrolled patients, those with TC ≥ 200 mg/dl showed longer median progression-free survival (mPFS; 6.6 vs. 4.7 months, P = .4), although not reaching statistical significance, and significantly longer median overall survival (mOS; 19.4 vs. 10.8 months, P = .02) compared to those with TC < 200 mg/dl. Conversely, patients with TG ≥150 mg/dl displayed shorter PFS (3.4 vs. 5.1 months, P = .02) and OS (7.1 vs. 12.9 months, P = .009) compared to those with TG <150 mg/dl. TC and TG were then combined in a "LIPID score" identifying three subgroups: good-risk (GR) (TC ≥200 mg/dl and TG <150 mg/dl), intermediate-risk (IR) (TC <200 mg/dl and TG <150 mg/dl or TC ≥200 mg/dl and TG ≥150 mg/dl) and poor-risk (PR) (TC <200 mg/dl and TG ≥150 mg/dl). The mPFS of GR, IR, and PR groups was 7.8, 4.3, and 2.5 months, respectively (P = .005); mOS of GR, IR, and PR was 20.4, 12.4, and 5.3 months, respectively (P < .001). At multivariable analysis, the PR profile represented an independent poor prognostic factor for both PFS and OS.
We developed a lipid score that defined subgroups of patients with cancer who differently benefit from ICIs. Further mechanistic insights are warranted to clarify the prognostic and predictive role of lipid profile components in patients treated with ICIs.
脂质谱的特定成分似乎对癌症的免疫活性有不同的影响,因此需要阐明它们在接受免疫检查点抑制剂 (ICI) 治疗的实体瘤患者中的预后作用。
我们回顾性收集了连续接受 ICI 治疗的实体瘤患者的基线临床病理特征,包括循环脂质谱(总胆固醇 [TC]、甘油三酯 [TG]、低密度脂蛋白 [LDL]、高密度脂蛋白 [HDL]),并研究了它们在预测临床结局中的作用。
在中位随访 32.9 个月时,在纳入的 430 名患者中,TC≥200mg/dl 的患者中位无进展生存期 (mPFS; 6.6 个月 vs. 4.7 个月,P=0.4) 较长,尽管未达到统计学意义,中位总生存期 (mOS; 19.4 个月 vs. 10.8 个月,P=0.02) 也显著更长,与 TC<200mg/dl 的患者相比。相反,TG≥150mg/dl 的患者 PFS(3.4 个月 vs. 5.1 个月,P=0.02)和 OS(7.1 个月 vs. 12.9 个月,P=0.009)较短。然后,TC 和 TG 被组合成一个“脂质评分”,确定了三个亚组:低危组(GR)(TC≥200mg/dl 且 TG<150mg/dl)、中危组(IR)(TC<200mg/dl 且 TG<150mg/dl 或 TC≥200mg/dl 且 TG≥150mg/dl)和高危组(PR)(TC<200mg/dl 且 TG≥150mg/dl)。GR、IR 和 PR 组的 mPFS 分别为 7.8、4.3 和 2.5 个月(P=0.005);GR、IR 和 PR 的 mOS 分别为 20.4、12.4 和 5.3 个月(P<0.001)。多变量分析显示,PR 特征是 PFS 和 OS 的独立不良预后因素。
我们开发了一种脂质评分,定义了不同程度受益于 ICI 治疗的癌症患者亚组。需要进一步的机制研究来阐明脂质谱成分在接受 ICI 治疗的患者中的预后和预测作用。