Department of Oncology and Dermatological Oncology, IDI-IRCCS, Rome, Italy.
Epidemiology Unit, IDI-IRCCS, Rome, Italy.
Clin Oncol (R Coll Radiol). 2022 Jan;34(1):e18-e24. doi: 10.1016/j.clon.2021.09.006. Epub 2021 Sep 23.
Cutaneous melanoma is one of the most immunogenic tumours. Immunotherapy with checkpoint inhibitors, such as anti-PD-1 antibodies, has significantly improved the prognosis in metastatic melanoma. However, only half of the patients respond to this therapy and have a favourable outcome. Identifying factors associated with treatment failure and early identification of responders are both important to select the best treatment approach for each patient. The aim of our study was to investigate clinical biomarkers of response to treatment with anti-PD-1 antibodies.
We selected all patients with stage IV melanoma (n = 147), subjected to first-line treatment with anti-PD-1 in the last 10 years. We investigated the associations between patients' different clinical features and progression-free survival, using the Cox proportional hazards models.
In the multivariate analysis, an increased risk of disease progression was observed among patients with stage M1d metastases (hazard ratio 3.30; 95% confidence interval 1.58-6.91), compared with patients with stage M1a-M1b. Moreover, the risk of progression was greater in patients with the Eastern Cooperative Oncology Group Performance Status (ECOG PS) 1 (hazard ratio 2.04; 95% confidence interval 1.02-4.06) and in patients with ECOG PS ≥ 2 (hazard ratio 2.19; 95% confidence interval 1.05-4.55) compared with ECOG PS 0. High levels of lactate dehydrogenase (hazard ratio 2.06; 95% confidence interval 1.18-3.59) and the presence of respiratory diseases (hazard ratio 4.14; 95% confidence interval 1.42-12.0) at the beginning of anti-PD-1 treatment were also associated with an increased risk of disease progression. In a subgroup analysis, neutrophil count and neutrophil/lymphocyte ratio before anti-PD-1 treatment were higher in patients who underwent disease progression.
In our study population, independent predictors of disease progression among patients treated with first-line anti-PD-1 were as follows: ECOG PS, staging, lactate dehydrogenase and the presence of respiratory diseases.
皮肤黑色素瘤是最具免疫原性的肿瘤之一。免疫疗法联合检查点抑制剂,如抗 PD-1 抗体,已显著改善转移性黑色素瘤患者的预后。然而,只有一半的患者对此治疗有反应,并获得良好的效果。确定与治疗失败相关的因素以及早期识别应答者对于为每位患者选择最佳治疗方法都很重要。本研究旨在探讨抗 PD-1 抗体治疗反应的临床生物标志物。
我们选择了过去 10 年中接受一线抗 PD-1 治疗的所有 IV 期黑色素瘤患者(n=147)。我们使用 Cox 比例风险模型,研究了患者不同临床特征与无进展生存期之间的关系。
多变量分析显示,与 M1a-M1b 期患者相比,M1d 期转移患者疾病进展的风险更高(危险比 3.30;95%置信区间 1.58-6.91)。此外,ECOG PS 1 (危险比 2.04;95%置信区间 1.02-4.06)和 ECOG PS≥2(危险比 2.19;95%置信区间 1.05-4.55)的患者进展风险大于 ECOG PS 0 的患者。在开始抗 PD-1 治疗时,乳酸脱氢酶水平升高(危险比 2.06;95%置信区间 1.18-3.59)和存在呼吸系统疾病(危险比 4.14;95%置信区间 1.42-12.0)也与疾病进展风险增加相关。在亚组分析中,抗 PD-1 治疗前中性粒细胞计数和中性粒细胞/淋巴细胞比值较高的患者疾病进展。
在本研究人群中,接受一线抗 PD-1 治疗的患者疾病进展的独立预测因素如下:ECOG PS、分期、乳酸脱氢酶和呼吸系统疾病。