Beta-blocker use is associated with improved relapse-free survival in patients with triple-negative breast cancer
- PMID: 21632501
- PMCID: PMC3139371
- DOI: 10.1200/JCO.2010.33.4441
Beta-blocker use is associated with improved relapse-free survival in patients with triple-negative breast cancer
Abstract
Purpose: To examine the association between beta-blocker (BB) intake, pathologic complete response (pCR) rates, and survival outcomes in patients with breast cancer treated with neoadjuvant chemotherapy.
Patients and methods: We retrospectively reviewed 1,413 patients with breast cancer who received neoadjuvant chemotherapy between 1995 and 2007. Patients taking BBs at the start of neoadjuvant therapy were compared with patients with no BB intake. Rates of pCR between the groups were compared using a χ² test. Cox proportional hazards models were fitted to determine the association between BB intake, relapse-free survival (RFS), and overall survival (OS).
Results: Patients who used BBs (n = 102) were compared with patients (n = 1,311) who did not. Patients receiving BBs tended to be older and obese (P < .001). The proportion of pCR was not significantly different between the groups (P = .48). After adjustment for age, race, stage, grade, receptor status, lymphovascular invasion, body mass index, diabetes, hypertension, and angiotensin-converting enzyme inhibitor use, BB intake was associated with a significantly better RFS (hazard ratio [HR], 0.52; 95% CI, 0.31 to 0.88) but not OS (P = .09). Among patients with triple-negative breast cancer (TNBC; n = 377), BB intake was associated with improved RFS (HR, 0.30; 95% CI, 0.10 to 0.87;P = .027) but not OS (HR, 0.35; 95% CI, 0.12 to 1.00;P = .05).
Conclusion: In this study, BB intake was associated with improved RFS in all patients with breast cancer and in patients with TNBC. Additional studies evaluating the potential benefits of beta-adrenergic blockade on breast cancer recurrence with a focus on TNBC are warranted.
Conflict of interest statement
Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.
Figures
Comment in
-
Expanding our therapeutic options: Beta blockers for breast cancer?J Clin Oncol. 2011 Jul 1;29(19):2612-6. doi: 10.1200/JCO.2011.35.8820. Epub 2011 May 31. J Clin Oncol. 2011. PMID: 21632500 No abstract available.
-
Targeted therapies: Using β-blockers to inhibit breast cancer progression.Nat Rev Clin Oncol. 2011 Aug 2;8(9):511-2. doi: 10.1038/nrclinonc.2011.123. Nat Rev Clin Oncol. 2011. PMID: 21808268
Similar articles
-
Ki-67 can be used for further classification of triple negative breast cancer into two subtypes with different response and prognosis.Breast Cancer Res. 2011 Mar 2;13(2):R22. doi: 10.1186/bcr2834. Breast Cancer Res. 2011. PMID: 21366896 Free PMC article.
-
Neoadjuvant chemotherapy is associated with improved survival compared with adjuvant chemotherapy in patients with triple-negative breast cancer only after complete pathologic response.Ann Surg Oncol. 2012 Jan;19(1):253-8. doi: 10.1245/s10434-011-1877-y. Epub 2011 Jul 2. Ann Surg Oncol. 2012. PMID: 21725686 Free PMC article.
-
Receptor status change from primary to residual breast cancer after neoadjuvant chemotherapy and analysis of survival outcomes.Clin Breast Cancer. 2015 Apr;15(2):153-60. doi: 10.1016/j.clbc.2014.09.006. Epub 2014 Oct 2. Clin Breast Cancer. 2015. PMID: 25454687
-
Beta-blockers in early-stage breast cancer: a systematic review and meta-analysis.ESMO Open. 2021 Apr;6(2):100066. doi: 10.1016/j.esmoop.2021.100066. Epub 2021 Feb 25. ESMO Open. 2021. PMID: 33639601 Free PMC article. Review.
-
Evaluation of Pathologic Complete Response as a Surrogate for Long-Term Survival Outcomes in Triple-Negative Breast Cancer.J Natl Compr Canc Netw. 2020 Aug;18(8):1096-1104. doi: 10.6004/jnccn.2020.7550. J Natl Compr Canc Netw. 2020. PMID: 32755985 Review.
Cited by
-
Multiple cancer cell types release LIF and Gal3 to hijack neural signals.Cell Res. 2024 Mar 11. doi: 10.1038/s41422-024-00946-z. Online ahead of print. Cell Res. 2024. PMID: 38467743
-
β2-Adrenoceptor Activation Favor Acquisition of Tumorigenic Properties in Non-Tumorigenic MCF-10A Breast Epithelial Cells.Cells. 2024 Jan 30;13(3):262. doi: 10.3390/cells13030262. Cells. 2024. PMID: 38334654 Free PMC article.
-
The Beta2-adrenergic agonist salbutamol synergizes with paclitaxel on cell proliferation and tumor growth in triple negative breast cancer models.Cancer Chemother Pharmacol. 2023 Dec;92(6):485-499. doi: 10.1007/s00280-023-04586-9. Epub 2023 Sep 19. Cancer Chemother Pharmacol. 2023. PMID: 37725114
-
β2-AR inhibition enhances EGFR antibody efficacy hampering the oxidative stress response machinery.Cell Death Dis. 2023 Sep 19;14(9):613. doi: 10.1038/s41419-023-06129-9. Cell Death Dis. 2023. PMID: 37723219 Free PMC article.
-
Using administrative healthcare data to evaluate drug repurposing opportunities for cancer: the possibility of using beta-blockers to treat breast cancer.Front Pharmacol. 2023 Aug 10;14:1227330. doi: 10.3389/fphar.2023.1227330. eCollection 2023. Front Pharmacol. 2023. PMID: 37637417 Free PMC article.
References
-
- Cohen S, Janicki-Deverts D, Miller GE. Psychological stress and disease. JAMA. 2007;298:1685–1687. - PubMed
-
- Rangarajan PN, Umesono K, Evans RM. Modulation of glucocorticoid receptor function by protein kinase A. Mol Endocrinol. 1992;6:1451–1457. - PubMed
-
- Dong Y, Aronsson M, Gustafsson JA, et al. The mechanism of cAMP-induced glucocorticoid receptor expression: Correlation to cellular glucocorticoid response. J Biol Chem. 1989;264:13679–13683. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous
