Circulating Cancer-Associated Macrophage-like Cells as a Blood-Based Biomarker of Response to Immune Checkpoint Inhibitors

Author:

Magri Valentina1ORCID,De Renzi Gianluigi2,Marino Luca3ORCID,De Meo Michela2ORCID,Siringo Marco1ORCID,Gelibter Alain1,Gareri Roberta4,Cataldi Chiara1ORCID,Giannini Giuseppe2ORCID,Santini Daniele1,Nicolazzo Chiara2ORCID,Gazzaniga Paola2ORCID

Affiliation:

1. Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy

2. Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy

3. Department of Mechanical and Aerospace Engineering, Sapienza University of Rome, 00184 Rome, Italy

4. UOC di Oncologia Medica, Ospedale Leopoldo Parodi Delfino, 00034 Colleferro, Italy

Abstract

Evidence has been provided that circulating cancer-associated macrophage-like cell (CAM-L) numbers increase in response to chemotherapy, with an inverse trend compared to circulating tumor cells (CTCs). In the era of evolving cancer immunotherapy, whether CAM-Ls might have a potential role as predictive biomarkers of response has been unexplored. We evaluated whether a serial blood evaluation of CTC to CAM-L ratio might predict response to immune checkpoint inhibitors in a cohort of non-small-cell lung cancer patients. At baseline, CTCs, CAM-Ls, and the CTC/CAM-L ratio significantly correlate with both progression-free survival (PFS) and overall survival (OS). The baseline CTC/CAM-L ratio was significantly different in early progressors (4.28 ± 3.21) compared to long responders (0.42 ± 0.47) (p = 0.001). In patients treated with immune checkpoint inhibitors, a CTC/CAM-L ratio ≤ 0.25 at baseline is associated with better PFS and OS. A baseline CTC/CAM-L ratio ≤ 0.25 is statistically significant to discriminate early progressions from durable response. The results of the present pilot study suggest that CAM-Ls together with CTCs could play an important role in evaluating patients treated with cancer immunotherapy.

Publisher

MDPI AG

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