Abstract

BackgroundMicroparticles (MPs) are extracellular vesicles that are associated with cancer development and progression. Advanced non-small cell lung cancer (NSCLC) still shows disease progression after multiple lines of treatment. Therefore, the objective of this study was to explore the correlation between circulating MPs and disease progression in advanced NSCLC, and to find a new method for concise and rapid determination of disease progression.MethodsPatients with advanced NSCLC admitted to hospital between October 2019 and October 2020 were included and divided into objective remission (OR) and progressive disease (PD) groups. The morphology of MPs was observed using transmission electron microscopy. The circulating total MPs, neutrophil MPs (NMPs), and platelet MPs (PMPs) before and after treatment were detected by flow cytometry, and a predictive model for disease progression in advanced NSCLC was developed.ResultsEighty-six patients were included; 60 in the OR group and 26 in the PD group. There was no significant difference in total MPs, NMPs, or PMPs at baseline between the two groups. After treatment, total MPs, NMPs, and PMPs were significantly higher in the PD than those in the OR group. Multivariate regression analysis showed that post-treatment NMPs≥160 events/μL(OR,3.748;95%CI,1.147–12.253,p = 0.029), PMPs≥80 events/μL(OR,10.968;95%CI,2.973–40.462,p < 0.0001) and neutrophil/lymphocyte ratio (NLR) ≥3.3 (OR,4.929;95%CI,1.483–16.375,p = 0.009) were independently associated with progression of advanced NSCLC. Post-treatment NMPs and PMPs combined with NLR were used to build a predictive model for progression of advanced NSCLC. The area under the curve was 0.825 (95%CI,0.715–0.934, p < 0.0001), optimal cut-off value was 16, sensitivity was 80.8%, and specificity was 88.3%.ConclusionNMPs and PMPs are associated with progression of advanced NSCLC. The predictive model for progression of advanced NSCLC, established combining NMPs, PMPs, and NLR, can screen out 80.8% of patients with PD. This is helpful for real-time accurate, concise and rapid assessment of disease progression and timely adjustment of drug therapy.Trial registrationChinese Clinical Trial Registry, ChiCTR1800020223. Registered 20 December 2018, http://www.chictr.org.cn/index.aspx.

Highlights

  • Lung cancer is a common malignancy, accounting for 11.6% of total cancer incidence and 18.4% of cancer deaths, and remains the leading cause of cancer death worldwide [1, 2]

  • neutrophil MPs (NMPs) and platelet MPs (PMPs) are associated with progression of advanced non-small cell lung cancer (NSCLC)

  • On the basis of circulating NMPs, PMPs, and neutrophil/lymphocyte ratio (NLR), we developed a predictive model for disease progression in advanced NSCLC, which suggests a high risk of disease progression when the prediction score is > 16

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Summary

Introduction

Lung cancer is a common malignancy, accounting for 11.6% of total cancer incidence and 18.4% of cancer deaths, and remains the leading cause of cancer death worldwide [1, 2]. In 2005, MPs were defined as cell-derived, extracellular vesicles of 0.1–1 μm diameter that lack a nucleus and the ability to synthesize proteins. They carry parentcell-derived proteins (e.g., signaling proteins, skeletal proteins, etc.), nucleic acids (e.g., miRNA, mRNA, DNA), and lipids, and have high level of membrane phosphatidylserine [8]. Advanced non-small cell lung cancer (NSCLC) still shows disease progression after multiple lines of treatment. The objective of this study was to explore the correlation between circulating MPs and disease progression in advanced NSCLC, and to find a new method for concise and rapid determination of disease progression

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