PD-L1+ aneuploid circulating tumor endothelial cells (CTECs) exhibit resistance to the checkpoint blockade immunotherapy in advanced NSCLC patients. (28th January 2020)

• Record Type: Journal Article
• Authors: Zhang, Lina; Zhang, Xinyong; Liu, Yanxia; Zhang, Tongmei; Wang, Ziyu; Gu, Meng; Li, Yilin; Wang, Daisy Dandan; Li, Weiying; Lin, Peter Ping
• Is Part Of: Cancer letters. Volume 469(2020)
• Page Start: 355
• Page End: 366
• Publication Date: 2020-01-28
• Subjects: Aneuploid CTC and CTEC -- Post-therapeutic karyotype shifting -- Cellular circulating tumor biomarker -- Liquid biopsy -- SE-iFISH; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2019.10.041
• Languages: English
• ISSNs: 0304-3835

Abstract

Abstract: Sustained angiogenesis and increased PD-L1 expression on endothelial and carcinoma cells contribute toward fostering an immunosuppressive microenvironment suitable for tumor growth. PD-L1 + CTCs were reported to associate with poor prognosis in NSCLC patients. However, whether or not aneuploid circulating tumor endothelial cells (CTECs) express PD-L1, then serve as a surrogate biomarker to evaluate immunotherapy efficacy remains unknown. In this study, a novel SE-iFISH strategy was established to comprehensively quantify and characterize a full spectrum of aneuploid CTCs and CTECs in advanced NSCLC patients subjected to second-line anti-PD-1 (nivolumab) immunotherapy. In situ co-detection of diverse subtypes of aneuploid CTCs and CTECs expressing PD-L1 and Vimentin was performed. The present clinical study demonstrated that significant amounts of PD-L1 + aneuploid CTCs and CTECs could be detected in histopathologic hPD-L1 - patients. In contrast to decreased PD-L1 + CTCs, the number of multiploid PD-L1 + CTECs (≥tetrasomy 8) undergoing post-therapeutic karyotype shifting increased in patients along with tumor progression following anti-PD-1 treatment. Progressive disease (PD) lung cancer patients possessing multiploid PD-L1 + CTECs had a significantly shorter PFS compared to those without PD-L1 + CTECs. In carcinoma patients, aneuploid CTCs and CTECs may exhibit a functional interplay with respect to tumor angiogenesis, progression, metastasis, and response to immunotherapy. Highlights: This is the first report to show the expression of PD-L1 on aneuploid CTECs. Multiploid (≥tetrasomy 8) PD-L1 + CTECs correlates with immunotherapy resistance. Post-immunotherapeutic PD patients possessing PD-L1 + CTECs have a shorter PFS.