Main Session
Sep 28
PQA 02 - Lung Cancer/Thoracic Malignancies, Patient Reported Outcomes/QoL/Survivorship, Pediatric Cancer

2448 - Identification of Dosimetric and Clinical Predictors for Post-Treatment Pulmonary Hospitalizations in NSCLC

04:45pm - 06:00pm PT
Hall F
Screen: 11
POSTER

Presenter(s)

Josiah Nieto, MD - University of Michigan, Ann Arbor, MI

J. D. Nieto1, W. Wang2, M. Schipper2, D. P. Bergsma1, J. A. Hayman2, H. Yin3, M. M. Dominello4, M. Zaki5, A. F. Dragovic1, L. L. Kestin6, P. A. Paximadis7, M. M. Matuszak1, S. R. Miller1, and S. Jolly1; 1Department of Radiation Oncology, University of Michigan, Ann Arbor, MI, 2University of Michigan, Ann Arbor, MI, 3Department of Biostatistics, University of Michigan, Ann Arbor, MI, 4Department of Radiation Oncology, Karmanos Cancer Center, Detroit, MI, 5Covenant HealthCare, Saginaw, MI, 6Michigan Healthcare Professionals/GenesisCare USA, Farmington Hills, MI, 7Department of Radiation Oncology, Corewell Health South, St. Joseph, MI

Purpose/Objective(s): Pulmonary events following radiation therapy (RT) for non-small cell lung cancer (NSCLC) can lead to morbidity and negatively affect outcomes. This study evaluates the predictive value of dose-volume parameters (mean lung dose [MLD], V5–V60) and clinical factors for post-treatment pulmonary hospitalizations. We seek to improve risk stratification and develop more comprehensive clinical decision-making tools.

Materials/Methods: Data were analyzed from a prospective statewide quality consortium. Eligible patients (2018-2024) included those with stage I-III NSCLC treated with definitive RT with available dosimetric data. Patients receiving surgery were excluded. Pulmonary hospitalizations were classified as pneumonitis, COPD, pneumonia, or other respiratory complications based on clinical diagnosis, with multiple classifications allowed for overlapping conditions. EQD2 dose distributions were calculated (a/ß = 3). Multivariable Cox proportional hazards models were used to identify predictors of hospitalization, and cumulative incidence estimates were calculated, accounting for competing risks of death. Variables were selected using a stepwise procedure, and interactions were tested for significance.

Results: Of 1407 patients, 310(19%) experienced a lung-related hospitalization. Median follow-up was 14 months. Pneumonitis, pneumonia, and COPD-related hospitalizations occurred in 34(2%), 156(10%), and 135(8%) patients, respectively. The 24-month cumulative incidence of pneumonitis, pneumonia, and COPD-related hospitalizations was 2.7%, 10.6%, and 12.2%, respectively. The cumulative incidence of any lung-related hospitalization was 24.4%. MLD was the strongest predictor of pneumonitis (HR = 1.24 per 1 Gy, p < 0.01) and overall lung-related hospitalizations (HR = 1.04 per 1 Gy, p < 0.01). The estimated 24-month cumulative incidence of lung-related hospitalization increased from 18% at MLD = 0 Gy to 35% at MLD = 20 Gy. Lung dosimetric factors are seen in table below. ECOG performance status (2 vs. 0/1), pre-existing COPD, and supplemental oxygen use were independently associated with increased hospitalization risk.

Conclusion: This analysis confirms that MLD and dose-volume metrics are key predictors of pulmonary hospitalizations in NSCLC. Clinical factors further refine risk assessment. Integrating dosimetric and clinical data can improve risk stratification and guide personalized treatment decisions.

Abstract 2448 - Table 1: Lung dosimetric factors and corresponding 24 month pulmonary hospitalization HR

Dose-Volume Parameter

HR (95% CI)

?2 value

MLD

1.037 (1.009-1.066)

0.0091

V5

1.007 (1.001-1.014)

0.0211

V10

1.009 (1.001-1.018

0.0331

V20

1.018 (1.003-1.032)

0.0147

V30

1.023 (1.004-1.043)

0.0191

V40

1.033 (1.006-1.060)

0.0143

V50

1.046 (1.010-1.084)

0.0109

V60

1.065 (1.011-1.122)

0.0180