Janka Eszter Anna, Ványai Beatrix, Szabó Imre Lőrinc, Toka-Farkas Tünde, Várvölgyi Tünde, Kapitány Anikó, Szegedi Andrea, Emri Gabriella
Department of Dermatology, MTA Centre of Excellence, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
ELKH-DE Allergology Research Group, Debrecen, Hungary.
Front Oncol. 2023 Aug 17;13:1237643. doi: 10.3389/fonc.2023.1237643. eCollection 2023.
Prognostic classification of metastatic melanoma patients treated with anti-PD-1 is of great interest to clinicians.
We aimed to determine the anti-PD-1 treatment related prognostic performance of demographics, clinical and histological prognostic markers and baseline serum S100B and LDH levels in advanced melanoma.
A total of 200 patients with unresectable metastatic melanoma were included in this retrospective study. 34.5% had stage M1c disease and 11.5% had stage M1d disease at the start of therapy. 30% had pT4b primary melanoma. 55.5% had elevated baseline serum S100B levels and 62.5% had elevated baseline serum LDH levels. We analysed the risk of death using univariate and multivariate Cox proportional-hazards models and the median overall (OS) and progression-free (PFS) survival using the Kaplan-Meier estimator.
The median follow-up time from the start of anti-PD-1 treatment in patients who were alive at the end of the study (N=81) was 37 months (range: 6.1-95.9). The multivariate Cox regression analysis showed that M1c stage (vs. M1a, p=0.005) or M1d stage at the start of therapy (vs. M1a, p=0.001), pT4b category (vs. pT1a, p=0.036), elevated baseline serum S100B levels (vs. normal S100B, p=0.008) and elevated LDH levels (vs. normal LDH, p=0.049) were independently associated with poor survival. The combination of M1d stage, elevated baseline serum S100B and LDH levels and pT4b category was associated with a very high risk of death (HR 4.72 [1.81; 12.33]). In the subgroup of patients with pT4b primary melanoma, the median OS of patients with normal serum S100B levels was 37.25 months [95% CI 11.04; 63.46]), while the median OS of patients with elevated serum S100B levels was 8.00 months [95% CI 3.49; 12.51]) (p<0.001); the median OS of patients with normal serum LDH levels was 41.82 months [95% CI 11.33; 72.32]), while the median OS of patients with elevated serum LDH levels was 12.29 months [95% CI 4.35; 20.23]) (p=0.002).
Our real-world study indicates that the prognostic role of primary melanoma parameters is preserved in anti-PD-1 treated stage IV patients. Furthermore, there seems to be perspective in combining clinical, histological and serum prognostic markers in a prognostic model.
接受抗PD-1治疗的转移性黑色素瘤患者的预后分类是临床医生非常感兴趣的。
我们旨在确定晚期黑色素瘤患者的人口统计学、临床和组织学预后标志物以及基线血清S100B和LDH水平与抗PD-1治疗相关的预后表现。
本回顾性研究共纳入200例不可切除的转移性黑色素瘤患者。治疗开始时,34.5%的患者处于M1c期,11.5%的患者处于M1d期。30%的患者原发性黑色素瘤为pT4b。55.5%的患者基线血清S100B水平升高,62.5%的患者基线血清LDH水平升高。我们使用单因素和多因素Cox比例风险模型分析死亡风险,并使用Kaplan-Meier估计器分析中位总生存期(OS)和无进展生存期(PFS)。
在研究结束时仍存活的患者(N=81)中,从开始抗PD-1治疗起的中位随访时间为37个月(范围:6.1-95.9)。多因素Cox回归分析显示,治疗开始时的M1c期(vs.M1a,p=0.005)或M1d期(vs.M1a,p=0.001)、pT4b类别(vs.pT1a,p=0.036)、基线血清S100B水平升高(vs.S100B正常,p=0.008)和LDH水平升高(vs.LDH正常,p=0.049)与生存不良独立相关。M1d期、基线血清S100B和LDH水平升高以及pT4b类别的组合与极高的死亡风险相关(HR 4.72[1.81;12.33])。在原发性黑色素瘤为pT4b的患者亚组中,血清S100B水平正常的患者中位OS为37.25个月[95%CI 11.04;63.46]),而血清S100B水平升高的患者中位OS为8.00个月[95%CI 3.49;12.51])(p<0.001);血清LDH水平正常的患者中位OS为41.82个月[95%CI 11.33;72.32]),而血清LDH水平升高的患者中位OS为12.29个月[95%CI 4.35;20.23])(p=0.002)。
我们的真实世界研究表明,原发性黑色素瘤参数在接受抗PD-1治疗的IV期患者中仍具有预后作用。此外,在预后模型中结合临床、组织学和血清预后标志物似乎具有前景。