Incidence and risk factors for pneumonitis due to trastuzumab Deruxtecan in metastatic breast cancer: a retrospective cohort study

Fam-trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate (ADC) that targets human epidermal growth factor receptor 2 (HER2) and delivers a topoisomerase inhibitor payload. T-DXd has been effectively used to treat metastatic breast cancer but causes pneumonitis in 10–15% of cases. Risk factors associated with T-DXd pneumonitis are not well described. What are the major clinical risk factors for T-DXd pneumonitis? We conducted a retrospective study of women with metastatic breast cancer at our institution treated with T-DXd as standard of care between 2020 and 2024. We collected clinical data, including demographics, relevant review of symptoms, molecular subtypes, prior treatments, and pulmonary comorbidities, from the electronic health record. A thoracic radiologist reviewed pre-treatment scans for the presence of interstitial lung abnormalities (ILAs). Radiation exposure variables were obtained from an institutional database. Pulmonologists reviewed all cases for the development of pneumonitis. We used univariable and multivariable Cox proportional hazard models to measure the association of clinical variables with the development of pneumonitis. Pneumonitis was observed in 19/203 patients (9.4%). In univariable analyses, pre-treatment shortness of breath (hazard ratio [HR] 3.9, 95% confidence interval [CI] 1.3–11.7), greater number of prior treatments (HR 1.2 per line, 95% CI 1.0-1.4), triple-negative breast cancer (HR 4.9, 95% CI 1.8–13.0), low HER-2 status (4.00 (95% CI: 1.43–11.11) and pre-treatment ILAs (HR 17, 95% CI 6.5–46) were associated with pneumonitis. In multivariable models, pre-treatment ILAs (HR 10.56, 95% CI 3.8-29.31, p < 0.0001) and HER2 (HR 0.30, 95% CI 0.09–0.96, p = 0.042) were the strongest predictors of pneumonitis, with a marginal association observed for V20 (HR 1.04, 95% CI 0.99–1.09, p = 0.081). Pre-treatment ILAs and HER2-low breast cancer are major risk factors for T-DXd pneumonitis.

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Journal
Breast Cancer Research
Published
2025-11-05
DOI
https://doi.org/10.1186/s13058-025-02151-1
Citations
1
Primary Topic
HER2/EGFR in Cancer Research
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article
Field-Weighted Citation Impact
1.05
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article

Incidence and risk factors for pneumonitis due to trastuzumab Deruxtecan in metastatic breast cancer: a retrospective cohort study

Nerea González, Vickie R. Shannon, J. Alejandro Madrigal, Rashmi K. Murthy et al.
1 citations
Breast Cancer Research
HER2/EGFR in Cancer Research
1.05
article

Incidence and risk factors for pneumonitis due to trastuzumab Deruxtecan in metastatic breast cancer: a retrospective cohort study

Nerea González, Vickie R. Shannon, J. Alejandro Madrigal, Rashmi K. Murthy, Roland L. Bassett, Lara Bashoura, Jason Aboudi Mouabbi, Mehmet Altan, Girish S. Shroff, Bora Lim, Saadia A. Faiz, Ajay Sheshadri, Felipe Soto-Lanza, Cihan Duran, Funda Meric‐Bernstam, Sarah Pasyar, Kay L. Medina, Melissa P. Mitchell, David Zhang, Colin Chan, Amber Su, Carlos Ignacio Rodriguez Reyna, Maria Azhar
article en
1 citations

Abstract

Fam-trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate (ADC) that targets human epidermal growth factor receptor 2 (HER2) and delivers a topoisomerase inhibitor payload. T-DXd has been effectively used to treat metastatic breast cancer but causes pneumonitis in 10–15% of cases. Risk factors associated with T-DXd pneumonitis are not well described. What are the major clinical risk factors for T-DXd pneumonitis? We conducted a retrospective study of women with metastatic breast cancer at our institution treated with T-DXd as standard of care between 2020 and 2024. We collected clinical data, including demographics, relevant review of symptoms, molecular subtypes, prior treatments, and pulmonary comorbidities, from the electronic health record. A thoracic radiologist reviewed pre-treatment scans for the presence of interstitial lung abnormalities (ILAs). Radiation exposure variables were obtained from an institutional database. Pulmonologists reviewed all cases for the development of pneumonitis. We used univariable and multivariable Cox proportional hazard models to measure the association of clinical variables with the development of pneumonitis. Pneumonitis was observed in 19/203 patients (9.4%). In univariable analyses, pre-treatment shortness of breath (hazard ratio [HR] 3.9, 95% confidence interval [CI] 1.3–11.7), greater number of prior treatments (HR 1.2 per line, 95% CI 1.0-1.4), triple-negative breast cancer (HR 4.9, 95% CI 1.8–13.0), low HER-2 status (4.00 (95% CI: 1.43–11.11) and pre-treatment ILAs (HR 17, 95% CI 6.5–46) were associated with pneumonitis. In multivariable models, pre-treatment ILAs (HR 10.56, 95% CI 3.8-29.31, p < 0.0001) and HER2 (HR 0.30, 95% CI 0.09–0.96, p = 0.042) were the strongest predictors of pneumonitis, with a marginal association observed for V20 (HR 1.04, 95% CI 0.99–1.09, p = 0.081). Pre-treatment ILAs and HER2-low breast cancer are major risk factors for T-DXd pneumonitis.

Breast Cancer ResearchVol. 27(1)
The University of Texas MD Anderson Cancer Center (US), The University of Texas Health Science Center (US), Pulmonary and Critical Care Associates (US), University of Houston (US), Columbia University (US), Texas A&M University (US), Tecnológico de Monterrey (MX)
Openalex Percentile: Top 16%
HER2/EGFR in Cancer Research
1.05
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