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QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line.

Publication ,  Journal Article
Dent, S; Moore, H; Fradley, M; Grace Rose, C; Stergiopoulos, S; Chen, C; Li, B; Guha, A
Published in: Cardiooncology
July 4, 2025

BACKGROUND: The risk of drug-induced corrected QT interval (QTc) prolongation is an important consideration in clinical decision-making for patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer (mBC). This retrospective analysis described concomitant QTc-prolonging medication use in patients with HR+/HER2- mBC who received first-line (1L) treatment with a cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) plus an aromatase inhibitor (AI). METHODS: This retrospective claims analysis utilized the Optum Clinformatics Data Mart database to identify patients with HR+/HER2- mBC who initiated 1L CDK4/6i plus AI treatment between January 2017 and March 2022. Exposure to QTc-prolonging medications (overall and by Torsades de Pointes [TdP] risk, per www.crediblemeds.org ) was assessed at index (i.e., CDK4/6i treatment initiation) and during follow-up (i.e., duration of CDK4/6i treatment) in the overall cohort and cohorts stratified by patient age. RESULTS: A total of 1517 patients met the study criteria; 33.8%, 35.5%, and 30.8% were aged < 65, 65-74, and ≥ 75 years, respectively. Exposure to ≥ 1 QTc-prolonging medication or ≥ 1 medication with known TdP risk was observed in 53.3% and 15.4% of patients at index, respectively, and 78.6% and 57.1% of patients during follow-up, respectively. Patients were exposed to QTc-prolonging medications for 54.6% of total person-time during follow-up. Patients aged ≥ 65 years had higher exposure to medications with conditional TdP risk than those aged < 65 years, primarily driven by increased diuretic use. CONCLUSIONS: QTc-prolonging medication use was common in patients with HR+/HER2- mBC receiving 1L CDK4/6i plus AI treatment, highlighting the importance of reviewing concomitant medications to inform CDK4/6i selection and patient monitoring while on treatment.

Duke Scholars

Published In

Cardiooncology

DOI

EISSN

2057-3804

Publication Date

July 4, 2025

Volume

11

Issue

1

Start / End Page

64

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3201 Cardiovascular medicine and haematology
 

Citation

APA
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MLA
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Dent, S., Moore, H., Fradley, M., Grace Rose, C., Stergiopoulos, S., Chen, C., … Guha, A. (2025). QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line. Cardiooncology, 11(1), 64. https://doi.org/10.1186/s40959-025-00364-z
Dent, Susan, Heather Moore, Michael Fradley, Chloe Grace Rose, Stella Stergiopoulos, Connie Chen, Benjamin Li, and Avirup Guha. “QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line.Cardiooncology 11, no. 1 (July 4, 2025): 64. https://doi.org/10.1186/s40959-025-00364-z.
Dent S, Moore H, Fradley M, Grace Rose C, Stergiopoulos S, Chen C, et al. QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line. Cardiooncology. 2025 Jul 4;11(1):64.
Dent, Susan, et al. “QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line.Cardiooncology, vol. 11, no. 1, July 2025, p. 64. Pubmed, doi:10.1186/s40959-025-00364-z.
Dent S, Moore H, Fradley M, Grace Rose C, Stergiopoulos S, Chen C, Li B, Guha A. QT STAR: concomitant QTc-prolonging medication use among patients with HR+/HER2- metastatic breast cancer receiving a CDK4/6 inhibitor in first line. Cardiooncology. 2025 Jul 4;11(1):64.
Journal cover image

Published In

Cardiooncology

DOI

EISSN

2057-3804

Publication Date

July 4, 2025

Volume

11

Issue

1

Start / End Page

64

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3201 Cardiovascular medicine and haematology