Purpose of ReviewNon-small cell lung cancer (NSCLC) is a biologically and clinically heterogeneous disease. In addition to tumor-intrinsic characteristics, clinical outcomes from immune checkpoint inhibitors (ICIs) are influenced by a variety of host-related factors. This review aims to summarize current evidence on how body composition, metabolic comorbidities, sex, and systemic inflammation shape anti-tumor immunity and affect immunotherapy efficacy.Recent FindingsEmerging data suggest that altered body composition, including obesity and sarcopenia, may modulate ICI outcomes, giving rise to the so-called "obesity paradox", which appears inconsistent across tumor types and may reflect disease-specific nutritional and immunological profiles. Likewise, metabolic disorders such as type 2 diabetes and dyslipidemia can promote chronic inflammation and immune exhaustion, potentially dampening ICI activity. Advances in cross-sectional imaging and molecular profiling are refining the characterization of host-tumor-immune interactions and providing novel predictive insights.SummaryHost-related determinants play an integral role in shaping response to ICIs in NSCLC. A deeper understanding of the dynamic continuum linking metabolism, body composition, systemic inflammation, and immune regulation may enable more precise patient stratification and open opportunities for personalized immunotherapy strategies.

Host-related Determinants of Response to Immunotherapy in Non-small Cell Lung Cancer: The Interplay of Body Composition, Metabolism, Sex and Immune Regulation / Santo, Valentina; Brunetti, Leonardo; Pecci, Federica; Peroni, Marianna; Barnini, Giulia; Paoloni, Francesco; Buti, Sebastiano; Tiseo, Marcello; Ricciuti, Biagio; Pinato, David James; Cortellini, Alessio. - In: CURRENT ONCOLOGY REPORTS. - ISSN 1523-3790. - 27:12(2025), pp. 1427-1447. [10.1007/s11912-025-01718-7]

Host-related Determinants of Response to Immunotherapy in Non-small Cell Lung Cancer: The Interplay of Body Composition, Metabolism, Sex and Immune Regulation

Pecci, Federica
Investigation
;
Peroni, Marianna
Investigation
;
Buti, Sebastiano
Investigation
;
Tiseo, Marcello
Investigation
;
2025-01-01

Abstract

Purpose of ReviewNon-small cell lung cancer (NSCLC) is a biologically and clinically heterogeneous disease. In addition to tumor-intrinsic characteristics, clinical outcomes from immune checkpoint inhibitors (ICIs) are influenced by a variety of host-related factors. This review aims to summarize current evidence on how body composition, metabolic comorbidities, sex, and systemic inflammation shape anti-tumor immunity and affect immunotherapy efficacy.Recent FindingsEmerging data suggest that altered body composition, including obesity and sarcopenia, may modulate ICI outcomes, giving rise to the so-called "obesity paradox", which appears inconsistent across tumor types and may reflect disease-specific nutritional and immunological profiles. Likewise, metabolic disorders such as type 2 diabetes and dyslipidemia can promote chronic inflammation and immune exhaustion, potentially dampening ICI activity. Advances in cross-sectional imaging and molecular profiling are refining the characterization of host-tumor-immune interactions and providing novel predictive insights.SummaryHost-related determinants play an integral role in shaping response to ICIs in NSCLC. A deeper understanding of the dynamic continuum linking metabolism, body composition, systemic inflammation, and immune regulation may enable more precise patient stratification and open opportunities for personalized immunotherapy strategies.
2025
Host-related Determinants of Response to Immunotherapy in Non-small Cell Lung Cancer: The Interplay of Body Composition, Metabolism, Sex and Immune Regulation / Santo, Valentina; Brunetti, Leonardo; Pecci, Federica; Peroni, Marianna; Barnini, Giulia; Paoloni, Francesco; Buti, Sebastiano; Tiseo, Marcello; Ricciuti, Biagio; Pinato, David James; Cortellini, Alessio. - In: CURRENT ONCOLOGY REPORTS. - ISSN 1523-3790. - 27:12(2025), pp. 1427-1447. [10.1007/s11912-025-01718-7]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/3043314
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