Serum Tumor Marker Dynamics as Predictive Biomarkers in NSCLC Chemo-Immunotherapy and Mono-Immunotherapy Maintenance: A Registry-Based Descriptive Study.

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2020-12-18 eCollection Date: 2020-01-01 DOI:10.2147/LCTT.S286228
David Lang, Wolfgang Haslinger, Kaveh Akbari, Mario Scala, Benedikt Hergan, Christian Asel, Andreas Horner, Romana Wass, Elmar Brehm, Bernhard Kaiser, Bernd Lamprecht
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引用次数: 6

Abstract

Objective: To evaluate serum tumor markers (STM) as predictive biomarkers in advanced non-small cell lung cancer (NSCLC) treated with chemo-immunotherapy.

Methods: Patients having received platinum-based chemo-(CHT) and PD-1/PD-L1-directed immune checkpoint inhibitor (ICI) combination therapy were retrospectively followed. Carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), cytokeratin-19 fragments (CYFRA 21-1) and neuron specific enolase (NSE) were routinely measured at NSCLC diagnosis. The marker with the highest relative elevation was defined "leading STM", its change was assessed between CHT-ICI as well as mono-ICI maintenance initiation and the respective subsequent restaging. Corresponding computed tomography evaluations were analyzed using response evaluation criteria in solid tumors (RECIST). For CHT-ICI combination and subsequent mono-ICI-maintenance therapy, leading STM and RECIST response were evaluated regarding progression-free (PFS) and overall survival (OS) in Kaplan-Meier analyses.

Results: Among 80 CHT-ICI patients (41% women, mean age 63 years), median PFS was 5 months (M;4,9), median OS was 15M (10,/). PFS was significantly (p=0.042) longer, when the leading STM had decreased at first restaging under CHT-ICI combination therapy (9M (5,12; n=41) vs 5M (3,6; n=16)). In the 54 (67.5%) patients who received subsequent mono-ICI maintenance therapy, STM decrease was similarly associated with significantly (p<0.001) longer PFS (16M (7,/; n=16) vs 3.5M (2,6; n=22)). Patients with radiologically stable or progressive disease and concomitant leading STM decrease had similar PFS in the CHT-ICI combination phase (4M (3,7; n=16) vs 4.5M (2,6; n=14)), but longer PFS in the mono-ICI maintenance setting (13M (7,16; n=10) vs 3M (2,4; n=17)). Median OS was not reached in most subgroups.

Conclusion: Leading STM dynamics provide predictive biomarker information additional to radiological response evaluation patients receiving CHT-ICI combination therapy, especially in the mono-ICI maintenance setting.

血清肿瘤标志物动态作为非小细胞肺癌化疗免疫治疗和单免疫治疗维持的预测性生物标志物:一项基于注册表的描述性研究。
目的:评价血清肿瘤标志物(STM)在晚期非小细胞肺癌(NSCLC)化疗免疫治疗中的预测作用。方法:对接受铂基化疗(CHT)和PD-1/ pd - l1定向免疫检查点抑制剂(ICI)联合治疗的患者进行回顾性随访。在诊断非小细胞肺癌时,常规检测癌胚抗原(CEA)、碳水化合物抗原19-9 (CA19-9)、细胞角蛋白19片段(CYFRA 21-1)和神经元特异性烯醇酶(NSE)。相对高度最高的标记物被定义为“领先STM”,评估其在CHT-ICI和单ici维持开始和各自随后的再分期之间的变化。采用实体瘤应答评价标准(RECIST)分析相应的计算机断层扫描评价。对于CHT-ICI联合治疗和随后的单一ici维持治疗,Kaplan-Meier分析评估了领先的STM和RECIST反应,包括无进展(PFS)和总生存期(OS)。结果:80例CHT-ICI患者中(41%为女性,平均年龄63岁),中位PFS为5个月(M;4,9),中位OS为15M(10,/)。当CHT-ICI联合治疗首次再分期时领先STM减少时,PFS显著延长(p=0.042) (9M (5,12;n=41) vs 5M (3,6;n = 16)。在54例(67.5%)接受后续单ici维持治疗的患者中,STM的减少与接受CHT-ICI联合治疗的患者的放射反应评估提供了预测性生物标志物信息,特别是在单ici维持环境中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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