Novel circulating tumor cell-based blood test for the assessment of PD-L1 protein expression in treatment-naïve, newly diagnosed patients with non-small cell lung cancer

We evaluated the analytical and clinical performance of a novel circulating tumor cell (CTC)-based blood test for determination of programmed death ligand 1 (PD-L1) protein expression status in real time in treatment-naïve non-small cell lung cancer (NSCLC) patients. CTCs were detected in 86% of pat...

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Veröffentlicht in:Cancer Immunology, Immunotherapy Immunotherapy, 2019-07, Vol.68 (7), p.1087-1094
Hauptverfasser: Chen, Yen-Lin, Huang, Wen-Chien, Lin, Feng-Ming, Hsieh, Huangpin B., Hsieh, Chia-Hsun, Hsieh, Ruey Kuen, Chen, Kuo-Wei, Yen, Ming-Hong, Lee, James, Su, Stephen, Marfatia, Twinkal, Chang, Shih-En, Sundar, Padma, Patterson, Bruce, Watson, Drew, Mei, Rui, Javey, Manana
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Sprache:eng
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Zusammenfassung:We evaluated the analytical and clinical performance of a novel circulating tumor cell (CTC)-based blood test for determination of programmed death ligand 1 (PD-L1) protein expression status in real time in treatment-naïve non-small cell lung cancer (NSCLC) patients. CTCs were detected in 86% of patients with NSCLC (I–IV) at the time of diagnosis, with a 67% PD-L1 positivity rate (≥ 1 PDL + CTC). Among 33 NSCLC patients with PD-L1 results available via both tissue immunohistochemistry (IHC) and CTC assays, 78.9% were positive according to both methods. The CTC test identified an additional ten cases that were positive for PD-L1 expression but that tested negative via IHC analysis. Detection of higher PD-L1 expression on CTCs compared to that in the corresponding tissue was concordant with data obtained using other platforms in previously treated patients. The concordance in PD-L1 expression between tissue and CTCs was approximately 57%, which is higher than that reported by others. In summary, evaluation of PD-L1 protein expression status on CTCs isolated from NSCLC patients is feasible. PD-L1 expression status on CTCs can be determined serially during the disease course, thus overcoming the myriad challenges associated with tissue analysis.
ISSN:0340-7004
1432-0851
DOI:10.1007/s00262-019-02344-6