Prognostic roles of hematological indicators in programmed cell death protein 1/programmed cell death ligand 1 inhibitors for small-cell lung cancer: a retrospective cohort study.

IF 2.1 3区 医学 Q3 RESPIRATORY SYSTEM
Journal of thoracic disease Pub Date : 2024-12-31 Epub Date: 2024-12-28 DOI:10.21037/jtd-24-1826
Jiya Du, Qian Zhang, Le Tian, Yishan Chen, Ye Tian, Wolfram C M Dempke, Hugo Arasanz, Ross Andrew Soo, Zhiguo Zhou, Qingju Meng, Yibing Liu
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引用次数: 0

Abstract

Background: Lung cancer is the main cause of cancer death in the world, with small-cell lung cancer (SCLC) accounting for about 10-15% of all lung cancers. Although programmed cell death protein 1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitors represent a major breakthrough in SCLC treatment, only a minority of patients will benefit and there is still a lack of accurate biomarkers to guide clinical application. Inflammation plays a crucial role in tumorigenesis, tumor development, metastasis, and drug resistance, but there is limited research on the predictive value of these inflammatory indicators in SCLC. The purpose of our study was to determine the influence of prognostic nutritional index (PNI), systemic immune inflammation (SII), and other indexes on the efficacy and prognosis of patients with SCLC treated with PD-1/PD-L1 inhibitors.

Methods: A total of 700 patients of SCLC treated with PD-1/PD-L1 inhibitors in the Fourth Hospital of Hebei Medical University from January 2019 to January 2023 were retrospectively analysed. Among these patients, 246 were included after the inclusion and exclusion criteria were applied. The basic clinical data of patients were collected, included age, sex, PD-1 or PD-L1 inhibitors and so on. The neutrophil:lymphocyte ratio (NLR), platelet:lymphocyte ratio (PLR), PNI, SII, and monocyte:lymphocyte ratio (MLR) were calculated. SPSS 27 software was employed for statistical analysis. As of 1st March 2023, all patients had received a post-diagnosis follow-up. The median follow-up time was 11.7 months.

Results: Among the 246 patients with SCLC receiving PD-1/PD-L1 inhibitor treatment. the overall response rate and disease control rate were 47.6% and 89.8%, respectively. Median progression-free survival (PFS) and median overall survival (OS) were 9.0 months and 21.4 months, respectively. Multivariate analysis showed that MLR [hazard ratio (HR) =0.631; P=0.01], and platelet (PLT) count (HR =1.641; P=0.009) were independent risk factors for PFS. NLR (HR =0.566, P=0.01) and lactate dehydrogenase (LDH) (HR =0.446; P=0.002) were independent risk factors for OS.

Conclusions: Among patients with SCLC treated with PD-1/PD-L1 inhibitors, those with high MLR and low PLT had shorter PFS, whilst patients with high NLR and LDH had a shorter OS. NLR and LDH may be used as prognostic biomarkers patients with SCLC treated with PD-1/PD-L1 inhibitors. The promising clinical application of NLR and LDH in efficacy prognostic indicators and beneficiary selection for SCLC immunotherapy is highlighted.

血液学指标在程序性细胞死亡蛋白1/程序性细胞死亡配体1抑制剂治疗小细胞肺癌中的预后作用:一项回顾性队列研究
背景:肺癌是全球癌症死亡的主要原因,其中小细胞肺癌(SCLC)约占所有肺癌的10-15%。尽管程序性细胞死亡蛋白1 (PD-1)/程序性细胞死亡配体1 (PD-L1)抑制剂代表了SCLC治疗的重大突破,但只有少数患者会受益,而且仍然缺乏准确的生物标志物来指导临床应用。炎症在肿瘤发生、肿瘤发展、转移和耐药过程中起着至关重要的作用,但这些炎症指标在SCLC中的预测价值研究有限。本研究旨在探讨预后营养指数(PNI)、全身免疫炎症(SII)等指标对PD-1/PD-L1抑制剂治疗SCLC患者疗效和预后的影响。方法:回顾性分析河北医科大学第四医院2019年1月至2023年1月接受PD-1/PD-L1抑制剂治疗的700例SCLC患者。其中246例患者经纳入和排除标准纳入。收集患者的基本临床资料,包括年龄、性别、PD-1或PD-L1抑制剂等。计算中性粒细胞:淋巴细胞比值(NLR)、血小板:淋巴细胞比值(PLR)、PNI、SII、单核细胞:淋巴细胞比值(MLR)。采用SPSS 27软件进行统计分析。截至2023年3月1日,所有患者均接受了诊断后随访。中位随访时间为11.7个月。结果:246例SCLC患者接受PD-1/PD-L1抑制剂治疗。总有效率为47.6%,疾病控制率为89.8%。中位无进展生存期(PFS)和中位总生存期(OS)分别为9.0个月和21.4个月。多因素分析显示MLR[危险比(HR) =0.631;P=0.01],血小板(PLT)计数(HR =1.641;P=0.009)是PFS的独立危险因素。NLR (HR =0.566, P=0.01)和乳酸脱氢酶(LDH) (HR =0.446;P=0.002)是OS的独立危险因素。结论:在接受PD-1/PD-L1抑制剂治疗的SCLC患者中,高MLR和低PLT患者的PFS较短,而高NLR和LDH患者的OS较短。NLR和LDH可作为经PD-1/PD-L1抑制剂治疗的SCLC患者的预后生物标志物。强调NLR和LDH在SCLC免疫治疗疗效预后指标和受益人选择方面的临床应用前景。
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来源期刊
Journal of thoracic disease
Journal of thoracic disease RESPIRATORY SYSTEM-
CiteScore
4.60
自引率
4.00%
发文量
254
期刊介绍: The Journal of Thoracic Disease (JTD, J Thorac Dis, pISSN: 2072-1439; eISSN: 2077-6624) was founded in Dec 2009, and indexed in PubMed in Dec 2011 and Science Citation Index SCI in Feb 2013. It is published quarterly (Dec 2009- Dec 2011), bimonthly (Jan 2012 - Dec 2013), monthly (Jan. 2014-) and openly distributed worldwide. JTD received its impact factor of 2.365 for the year 2016. JTD publishes manuscripts that describe new findings and provide current, practical information on the diagnosis and treatment of conditions related to thoracic disease. All the submission and reviewing are conducted electronically so that rapid review is assured.
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