Circulating T-cell Immunosenescence in Patients with Advanced Non-small Cell Lung Cancer Treated with Single-agent PD-1/PD-L1 Inhibitors or Platinum-based Chemotherapy

• Published in: Clinical cancer research Vol. 27; no. 2; pp. 492 - 503
• Main Authors: Ferrara, Roberto, Naigeon, Marie, Auclin, Edouard, Duchemann, Boris, Cassard, Lydie, Jouniaux, Jean-Mehdi, Boselli, Lisa, Grivel, Jonathan, Desnoyer, Aude, Mezquita, Laura, Texier, Matthieu, Caramella, Caroline, Hendriks, Lizza, Planchard, David, Remon, Jordi, Sangaletti, Sabina, Proto, Claudia, Garassino, Marina C, Soria, Jean-Charles, Marabelle, Aurelien, Voisin, Anne-Laure, Farhane, Siham, Besse, Benjamin, Chaput, Nathalie
• Format: Journal Article
• Language: English
• Published: United States 15.01.2021
• ISSN: 1078-0432; 1557-3265
• DOI: 10.1158/1078-0432.CCR-20-1420

CD28, CD57, and KLRG1 have been previously identified as markers of T-cell immunosenescence. The impact of immunosenescence on anti-PD(L)-1 (ICI) or platinum-based chemotherapy (PCT) in patients with advanced non-small cell lung cancer (aNSCLC) is unknown. The percentage of CD28 , CD57 , KLRG1 among CD8 T cells [senescent immune phenotype (SIP)] was assessed by flow cytometry on blood from patients with aNSCLC before single-agent ICI (discovery cohort). A SIP cut-off was identified by log-rank maximization method and patients with aNSCLC treated with ICI (validation cohort) or PCT were classified accordingly. Proliferation and functional properties of SIP CD8 T cells were assessed . In the ICI discovery cohort ( = 37), SIP cut-off was 39.5%, 27% of patients were SIP . In the ICI validation cohort ( = 46), SIP status was found in 28% of patients and significantly correlated with worse objective response rate (ORR; 0% vs. 30%, = 0.04), median progression-free survival (PFS) [1.8 (95% confidence interval (CI), 1.3-NR) vs. 6.4 (95% CI, 2-19) months, = 0.009] and median overall survival, OS [2.8 (95% CI, 2.0-NR) vs. 20.8 (95% CI, 6.0-NR) months, = 0.02]. SIP status was significantly associated with circulating specific immunephenotypes, lower CD8 T cells proliferation, lower IL2 and higher TNFα and IFNγ production. In the ICI-pooled population ( = 83), SIP status did not correlate with any clinical characteristics and it was associated with significantly worse ORR, PFS, and OS. In PCT cohort ( = 61), 11% of patients were SIP . SIP status did not correlate with outcomes upon PCT. Circulating T-cell immunosenescence is observed in up to 28% of patients with aNSCLC and correlates with lack of benefit from ICI but not from PCT. .