Risk factors and long-term prognostic impact of trastuzumab deruxtecan-related interstitial lung disease in metastatic breast cancer.

1043 Background: Trastuzumab deruxtecan (T-DXd) has demonstrated substantial efficacy in HER2-positive and HER2-low metastatic breast cancer (MBC). Interstitial lung disease (ILD), however, remains a clinically significant safety concern. While ILD incidence has been reported, its long-term prognostic impact and associated risk factors are not well established. Methods: This retrospective, single-center study evaluated patients with MBC treated with T-DXd. ILD was defined as clinically and radiologically confirmed ILD, which led to T-DXd discontinuation per institutional protocol. Time to treatment failure (TTF) and overall survival (OS) were analyzed according to ILD occurrence. Potential clinical and treatment-related risk factors for ILD were assessed using univariable and penalized multivariable Cox regression models. Results: At a median follow-up of 12.7 months, 15 of 132 patients (11.4%) developed ILD leading to treatment discontinuation. Among these 15 patients, 9 (60%) had grade 1 disease, 3 (20%) had grade 2, and 3 (20%) had grade 3 disease; no grade 4 or fatal events were observed. There were no significant differences in TTF (P = 0.59) or OS (P = 0.21) between patients with and without ILD. Among patients who developed ILD, onset occurred significantly earlier in those with HER2-low disease compared with HER2-positive disease (median 6.0 vs. 14.6 months, P = 0.029). In univariable analyses, age ≥65 years (HR 3.39, 95% CI 1.18-9.68; P = 0.023), prior immune checkpoint inhibitor (ICI) therapy (HR 4.74, 95% CI 1.01-22.34; P = 0.049), and prior abemaciclib exposure (HR 4.11, 95% CI 1.19-14.14; P = 0.025) were significantly associated with ILD. In the penalized multivariable model, prior abemaciclib exposure remained the only independent risk factor (HR 10.38, 95% CI 1.07-NA; P = 0.042). Conclusions: Although ILD onset tended to occur earlier in HER2-low MBC, its development did not significantly affect long-term TTF or OS. Prior exposure to abemaciclib is a significant independent risk factor for T-DXd-related ILD, warranting careful monitoring in this population.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-05-27
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.1043
Primary Topic
Advanced Breast Cancer Therapies
Type
article
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article

Risk factors and long-term prognostic impact of trastuzumab deruxtecan-related interstitial lung disease in metastatic breast cancer.

M. Kuno, Mami Kurata, Lina Inagaki, Toshimi Takano et al.
Journal of Clinical Oncology
Advanced Breast Cancer Therapies
article

Risk factors and long-term prognostic impact of trastuzumab deruxtecan-related interstitial lung disease in metastatic breast cancer.

M. Kuno, Mami Kurata, Lina Inagaki, Toshimi Takano, Takayuki Ueno, Meiko Nishimura, Mari Hosonaga, Yukinori Ozaki, Jun Masuda, Takayuki Kobayashi, Yosuke Aoyama
article en

Abstract

1043 Background: Trastuzumab deruxtecan (T-DXd) has demonstrated substantial efficacy in HER2-positive and HER2-low metastatic breast cancer (MBC). Interstitial lung disease (ILD), however, remains a clinically significant safety concern. While ILD incidence has been reported, its long-term prognostic impact and associated risk factors are not well established. Methods: This retrospective, single-center study evaluated patients with MBC treated with T-DXd. ILD was defined as clinically and radiologically confirmed ILD, which led to T-DXd discontinuation per institutional protocol. Time to treatment failure (TTF) and overall survival (OS) were analyzed according to ILD occurrence. Potential clinical and treatment-related risk factors for ILD were assessed using univariable and penalized multivariable Cox regression models. Results: At a median follow-up of 12.7 months, 15 of 132 patients (11.4%) developed ILD leading to treatment discontinuation. Among these 15 patients, 9 (60%) had grade 1 disease, 3 (20%) had grade 2, and 3 (20%) had grade 3 disease; no grade 4 or fatal events were observed. There were no significant differences in TTF (P = 0.59) or OS (P = 0.21) between patients with and without ILD. Among patients who developed ILD, onset occurred significantly earlier in those with HER2-low disease compared with HER2-positive disease (median 6.0 vs. 14.6 months, P = 0.029). In univariable analyses, age ≥65 years (HR 3.39, 95% CI 1.18-9.68; P = 0.023), prior immune checkpoint inhibitor (ICI) therapy (HR 4.74, 95% CI 1.01-22.34; P = 0.049), and prior abemaciclib exposure (HR 4.11, 95% CI 1.19-14.14; P = 0.025) were significantly associated with ILD. In the penalized multivariable model, prior abemaciclib exposure remained the only independent risk factor (HR 10.38, 95% CI 1.07-NA; P = 0.042). Conclusions: Although ILD onset tended to occur earlier in HER2-low MBC, its development did not significantly affect long-term TTF or OS. Prior exposure to abemaciclib is a significant independent risk factor for T-DXd-related ILD, warranting careful monitoring in this population.

Journal of Clinical OncologyVol. 44(16_suppl)
The Cancer Institute Hospital (JP), Japanese Foundation For Cancer Research (JP)
Good health and well-being
Openalex Percentile: Top 8%
Advanced Breast Cancer Therapies
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