# Influence of Hypertension Management on Survival in Patients With Metastatic Breast Cancer

**Authors:** Reina Haque, Amrita Mukherjee, Lie Hong Chen, Tiffany A. Hogan, Moira Brady‐Rogers, Zheng Gu, Ariel Silverman, Ana Barac, Lauren P. Wallner

PMC · DOI: 10.1002/cam4.71642 · Cancer Medicine · 2026-02-26

## TL;DR

Managing hypertension with multiple medications may help extend life for women with metastatic breast cancer, especially for Hispanic and Black patients.

## Contribution

This study identifies that polytherapy for hypertension is associated with reduced mortality in metastatic breast cancer patients.

## Key findings

- Patients on antihypertensive polytherapy had 38% lower all-cause mortality risk compared to monotherapy.
- Hispanic patients showed the greatest benefit from polytherapy, with a 60% reduction in mortality risk.
- Breast cancer mortality was also lower in polytherapy users, especially with good medication adherence.

## Abstract

Although nearly half of women with metastatic breast cancer (mBC) have hypertension, it is unclear whether hypertension management improves survival. We examined the influence of pharmacologic hypertension management on all‐cause and breast cancer‐specific mortality in patients with mBC.

We conducted a longitudinal cohort study of 1332 female patients with de novo mBC diagnosed 2008–2020, followed through 2021. We calculated person‐year (PY) rates of all‐cause and breast cancer mortality by use of antihypertensives (monotherapy or polytherapy [one vs. multiple drug classes]). Multivariable Cox regression was used to estimate the association between antihypertensives and mortality.

Overall, 48.4% of patients with mBC had hypertension, which was greatest in Black women (64.6%). During follow‐up, 52.9% were treated with antihypertensive medications (20.3% monotherapy; 32.5% polytherapy). All‐cause mortality rates were lower in the polytherapy (21.4/100 PY) versus monotherapy (28.5/100 PY) group. All‐cause mortality risk was 38% lower (adjusted HR = 0.62; 95% CI: 0.47–0.82) in the polytherapy group vs. monotherapy. This protection was significantly greater in Hispanic patients (HR = 0.40; 95% CI: 0.20–0.84) and suggested in Black patients (HR = 0.48; 95% CI: 0.22–1.05). Similarly, breast cancer mortality was lower in those treated with polytherapy versus monotherapy, particularly those with good medication adherence (HR = 0.43; 95% CI: 0.24–0.77).

In patients with mBC, all‐cause mortality risk was lower among those treated with antihypertensive polytherapy versus monotherapy, with the greatest risk attenuation seen among Hispanic women. Additional prospective studies are needed to examine comorbidity management strategies that may help patients with mBC extend life, particularly including women of color.

In a cohort of 1332 patients with metastatic breast cancer, 52.9% were treated with antihypertensive medications (20.3% monotherapy; 32.5% polytherapy). All‐cause mortality risk was 38% lower (adjusted HR; 95% CI: 0.62; 0.47–0.82) in the antihypertensive polytherapy group vs. monotherapy, and this protection was significantly greater in Hispanic patients (HR = 0.40; 95% CI: 0.20–0.84) and suggested in Black patients (HR = 0.48; 95% CI: 0.22–1.05).

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** obesity (MESH:D009765), Breast Cancer (MESH:D001943), nerve and functional damage (MESH:D000080902), Hypertension (MESH:D006973), pain (MESH:D010146), Death (MESH:D003643), dyslipidemia (MESH:D050171), cardiometabolic conditions (MESH:D024821), Health (OMIM:603663), Diabetes (MESH:D003920), stage IV disease (MESH:D007676), Cancer (MESH:D009369)
- **Chemicals:** antidiabetic medications (-)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936983/full.md

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Source: https://tomesphere.com/paper/PMC12936983