4.4 Article

PD-L1 Expression in Circulating Tumor Cells as a Promising Prognostic Biomarker in Advanced Non-small-cell Lung Cancer Treated with Immune Checkpoint Inhibitors

期刊

CLINICAL LUNG CANCER
卷 22, 期 5, 页码 423-431

出版社

CIG MEDIA GROUP, LP
DOI: 10.1016/j.cllc.2021.03.005

关键词

Advanced cancer; NSCLC; CTCs; PD-1; Predictive; Immune Checkpoint

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资金

  1. IRC -Fondazione AIRC per la Ricerca sul Cancro [19026]

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This study found that PD-L1 expression on CTCs is correlated with overall survival in lung cancer patients, while CTC number is associated with baseline tumor size.
Biomarkers for immunotherapy represent a clinical need. Circulating tumor cells (CTCs) are associated with a worse outcome. This is a prospective single-center cohort study enrolling 39 patients with non-small-cell lung cancer. A median overall survival of 2.2, 3.7, and 16 months was observed in patients with negative CTC, positive CTC, and no CTC detectable, respectively. No correlation was found between PD-L1 expression on CTCs and on tumor tissue. CTCs were correlated with baseline tumor size. PD-L1 on CTCs is a promising biomarker. Background: Circulating tumor cells (CTCs) are a promising source of biological information in cancer. Data correlating PD-L1 expression in CTCs with patients' response to immune checkpoint inhibitors (ICIs) in non-small-cell lung cancer (NSCLC) are still lacking. Methods: This is a prospective single-center cohort study enrolling patients with advanced NSCLC. CTCs were identified and counted with the CellSearch system. PD-L1 expression on CTCs was assessed with phycoerythrin-conjugated anti-human PD-L1 antibody, clone MIH3 (BioLegend, USA). Primary endpoint was the correlation between the CTCs PD-L1 expression and overall survival (OS). Among secondary objectives, we evaluated the correlation between PD-L1 expression on CTCs and matched tumor tissue and the correlation of CTC number and baseline tumor size (BTS). Results: Thirty-nine patients treated with anti-PD-1/PD-L1 agents as second- or third-line therapy were enrolled. Patients were divided into 3 groups: no CTC detectable (CTCnull, n = 15), PD-L1 positive CTC (CTCpos, n = 13), and PD-L1 negative CTC (CTCneg, n = 11). Median OS in patients with CTCneg was 2.2 months, 95% confidence interval (CI), 0.8-3.6 (reference) versus 3.7 months, 95% CI, 0.1-7.5 (hazard ratio [HR] 0.33; 95% CI, 0.13-0.83; P=.019) in patients with CTCpos versus 16.0 months, 95% CI, 2.2-29.8 (HR 0.17; 95% CI, 0.06-0.45; P<.001) in patients with CTCnull. No correlation was found between PD-L1 expression on CTCs and on tumor tissue. CTC number was correlated with BTS. Conclusion: PD-L1 expression on CTCs is a promising biomarker in patients with NSCLC treated with ICIs. Further validation as predictive biomarker is needed. (C) 2021 Elsevier Inc. All rights reserved.

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