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Circulating Cancer-Associated Macrophage-like Cells as a Blood-Based Biomarker of Response to Immune Checkpoint Inhibitors.
Magri, Valentina; De Renzi, Gianluigi; Marino, Luca; De Meo, Michela; Siringo, Marco; Gelibter, Alain; Gareri, Roberta; Cataldi, Chiara; Giannini, Giuseppe; Santini, Daniele; Nicolazzo, Chiara; Gazzaniga, Paola.
Afiliação
  • Magri V; Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
  • De Renzi G; Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
  • Marino L; Department of Mechanical and Aerospace Engineering, Sapienza University of Rome, 00184 Rome, Italy.
  • De Meo M; Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
  • Siringo M; Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
  • Gelibter A; Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
  • Gareri R; UOC di Oncologia Medica, Ospedale Leopoldo Parodi Delfino, 00034 Colleferro, Italy.
  • Cataldi C; Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
  • Giannini G; Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
  • Santini D; Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
  • Nicolazzo C; Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
  • Gazzaniga P; Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Int J Mol Sci ; 25(7)2024 Mar 28.
Article em En | MEDLINE | ID: mdl-38612563
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Células Neoplásicas Circulantes Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Células Neoplásicas Circulantes Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália