Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, 84084, Fisciano, SA, Italy.
Melanoma, Cancer Immunotherapy and Innovative Therapies O.U, National Cancer Institute "G. Pascale", Naples, Italy.
J Transl Med. 2017 Dec 4;15(1):244. doi: 10.1186/s12967-017-1348-8.
Nivolumab is an anti-PD1 checkpoint inhibitor active in patients with advanced melanoma and as adjuvant therapy in high-risk metastatic melanoma patients.
In this single-center retrospective analysis, we investigated the CD73 enzyme activity in patients with metastatic melanoma stage IV and its correlation with the response to nivolumab. The soluble CD73 (sCD73) enzyme activity was measured in the serum of 37 melanoma patients before receiving nivolumab and the Harrel's C index was used to find the best cut-off for this biomarker. The multivariate Cox proportional hazard model was used to evaluate the prognostic value of CD73 enzyme activity for survival and progression-free survival.
Our results show that high levels of sCD73 enzyme activity were significantly associated with poor overall survival and progression-free survival in patients with metastatic melanoma. The median progression-free survival was 2.6 months [95% confidence interval (CI) 1.9-3.3] in patients with high sCD73 enzyme activity (> 27.8 pmol/min/mg protein), and 14.2 months (95% CI 4.6-23.8) in patients with lower CD73 enzyme activity, when patients were follow-up for a median of 24 months range. The median overall survival was not reached in patients with low sCD73 activity (< 27.8 pmol/min/mg protein) compared with 6.1 months (95% CI 0-14.8) in patients with higher sCD73 activity. In multivariate analyses, the sCD73 enzyme activity emerged as the strongest prognostic factor for overall survival and progression-free survival. Elevated basal levels of sCD73 enzyme activity, before starting nivolumab treatment, were associated with lower response rates to therapy.
We observed a significant association between the activity of sCD73 in the blood and clinical outcomes in patients with metastatic melanoma stage IV, receiving nivolumab. Although our results need to be confirmed and validated, we suggest that sCD73 might be used as serologic prognostic biomarker. Potentially evaluating sCD73 enzyme activity in the peripheral blood before treatment could help to estimate the response to nivolumab.
尼伏鲁单抗是一种抗 PD-1 检查点抑制剂,对晚期黑色素瘤患者有效,也可作为高危转移性黑色素瘤患者的辅助治疗药物。
在这项单中心回顾性分析中,我们研究了转移性黑色素瘤 IV 期患者的 CD73 酶活性及其与尼伏鲁单抗反应的相关性。在接受尼伏鲁单抗治疗前,我们检测了 37 名黑色素瘤患者血清中的可溶性 CD73(sCD73)酶活性,并使用 Harrel 的 C 指数来确定该生物标志物的最佳截断值。多变量 Cox 比例风险模型用于评估 CD73 酶活性对生存和无进展生存期的预后价值。
我们的结果表明,高水平的 sCD73 酶活性与转移性黑色素瘤患者的总生存期和无进展生存期不良显著相关。在中位随访 24 个月时,高 sCD73 酶活性(>27.8 pmol/min/mg 蛋白)患者的中位无进展生存期为 2.6 个月(95%CI 1.9-3.3),而 sCD73 酶活性较低的患者为 14.2 个月(95%CI 4.6-23.8)。sCD73 酶活性低的患者(<27.8 pmol/min/mg 蛋白)的中位总生存期未达到,而 sCD73 酶活性较高的患者(>27.8 pmol/min/mg 蛋白)为 6.1 个月(95%CI 0-14.8)。在多变量分析中,sCD73 酶活性是总生存期和无进展生存期的最强预后因素。在开始接受尼伏鲁单抗治疗前,sCD73 酶活性基础水平升高与治疗反应率降低相关。
我们观察到接受尼伏鲁单抗治疗的转移性黑色素瘤 IV 期患者血液中 sCD73 活性与临床结局之间存在显著关联。尽管我们的结果需要得到证实和验证,但我们建议 sCD73 可能作为血清学预后标志物。在治疗前评估外周血中的 sCD73 酶活性可能有助于估计对尼伏鲁单抗的反应。