Diffusing capacity for carbon monoxide (DLCO) change and outcome in advanced non-small cell lung cancer (aNSCLC) treated with immune checkpoint inhibitors (ICIs).

A Angela Montes (Hospital Clinic - IDIBAPS, Barcelona, Spain) A Alfredo Sanchez (Consorcio Hospitalario Provincial de Castellón, Castellon De La Plana, Spain) M Maria Arnal Rondán (Medical Oncology Service, Hospital Provincial de Castellón, Castellón, Spain) S Sara Cases (Hospital Provincial de Castellón, Castellón, Spain) J Jorge Soler (Hospital Provincial de Castellon, Castellón, Spain) I Isabel Tena (Hospital Provincial Castellón, Castellón, Spain) B Blanca Navarro (Hospital Provincial de Castellón, Castellón, Spain) D Daiana Timacheva (Hospital Provincial de Castellón, Castellón, Spain) M Manuel Modesto (Hospital Provincial de Castellón, Castellon, Spain) D David Lorente (Fundación Instituto Valenciano de Oncologia, Valencia, Spain)

Abstract

e20602 Background: Despite recent therapeutic advances, identifying effective prognostic markers in aNSCLC remains an unmet need. DLC) has shown prognostic value in non-oncological pulmonary conditions but is underexplored in predicting outcomes in aNSCLC. We aimed to evaluate the prognostic value of DLCO changes following treatment with ICIs. Methods: The NEUMOTOX study, a prospective observational study, enrolled aNSCLC patients undergoing treatment with ICI, with or without chemotherapy, from August 2022 to April 2024. DLCO was measured at baseline and at 3-6, 9, and 12 weeks. Using Cox proportional hazards models, the analysis specifically focused on the 6-week data to evaluate the relationship between early DLCO changes and OS and PFS, adjusting for ECOG, LIPI score, and PDL1 expression. Results: 47 patients had evaluable baseline and 6-week post-baseline DLCO measurements. The median baseline DLCO was 59%. 15 (32%) patients experienced a ≥15% reduction in DLCO at 6 weeks. Patients with DLCO decrease experienced lower OS (NR vs 12.5m; 1yr-OS 78.6% vs 53.8%; HR 3.7; p=0.011) and rPFS (7.7 vs 4m; HR 3.8; p=0.003) rates, in unadjusted and adjusted cox-regression models (Table 1 ). Conclusions: Significant reductions in DLCO early during ICI therapy are associated with poorer outcomes in aNSCLC patients. Monitoring DLCO changes could serve as an effective prognostic tool. Further research is needed to validate DLCO as a prognostic biomarker in clinical practice. Multivariable OS and rPFS model. Overall Survival rPFS Variable HR (95%CI); p-value HR (95%CI); p-value Baseline DLCO 1.04 (0.99-1.1);p=0.1 1.04 (1.01-1.08); p=0.011 DLCO ≥15% decrease 7.5 (1.7-33);p=0.009 7.6 (1.8-31.6); p=0.006 PLD1 (0, 1-50%, ≥50%) 0.17 (0.05-0.55); p=0.003 0.93 (0.47-1.86); p=0.8 ECOG 13.2 (1.9-50); p=0.01 1.35 (0.44-4.2); p=0.06 LIPI score 26 (4-55); p<0.001 1.6 (0.65-3.95); p=0.3

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

A

Angela Montes

Hospital Clinic - IDIBAPS, Barcelona, Spain

A

Alfredo Sanchez

Consorcio Hospitalario Provincial de Castellón, Castellon De La Plana, Spain

M

Maria Arnal Rondán

Medical Oncology Service, Hospital Provincial de Castellón, Castellón, Spain

S

Sara Cases

Hospital Provincial de Castellón, Castellón, Spain

J

Jorge Soler

Hospital Provincial de Castellon, Castellón, Spain

I

Isabel Tena

Hospital Provincial Castellón, Castellón, Spain

B

Blanca Navarro

Hospital Provincial de Castellón, Castellón, Spain

D

Daiana Timacheva

Hospital Provincial de Castellón, Castellón, Spain

M

Manuel Modesto

Hospital Provincial de Castellón, Castellon, Spain

D

David Lorente

Fundación Instituto Valenciano de Oncologia, Valencia, Spain