Neutrophil-to-lymphocyte ratio as a predictor of survival in patients with triple-negative breast cancer.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 16 08 2018
accepted: 16 12 2018
pubmed: 4 1 2019
medline: 2 7 2019
entrez: 4 1 2019
Statut: ppublish

Résumé

Peripheral blood lymphopenia and elevated neutrophil-to-lymphocyte ratio (NLR) have been associated with poor outcomes in various malignancies. However, existing literature has largely focused on baseline parameters. The aim of this study is to assess the impact of radiation therapy (RT) and chemotherapy on absolute lymphocyte counts (ALC) and NLR in relation to survival outcomes in patients with triple-negative breast cancer (TNBC). A retrospective analysis was performed on 126 patients with TNBC treated at Washington University between 2005 and 2010. Cox proportional hazard model with time-varying covariates was applied to estimate the effect of time-varying ALC and NLR separately on overall survival (OS) and disease-free survival (DFS). All patients received RT and 112 patients received either neoadjuvant chemotherapy or adjuvant chemotherapy, or both. Patients deceased had lower ALC and higher NLR compared to patients alive throughout the treatment course, even 1 year after treatment completion (ALC, 1 vs. 1.3, P = 0.03 and NLR, 3.9 vs. 2.6, P = 0.03). High ALC was associated with superior OS on both continuous and binary scales (cutoff of 1 K/ul) (HR 0.14; 95% CI 0.05-0.34; P < 0.001 and HR 0.28; 95% CI 0.13-0.61; P = 0.01, respectively). Additionally, high NLR was weakly associated with inferior OS on continuous scales (HR 1.1; 95% CI 1.06-1.15; P < 0.001). Post-treatment lymphopenia and NLR elevation can persist until 1 year after treatment completion. Both portend shorter survival for patients with TNBC. Our data support the use of ALC and NLR to identify high risk patients who may benefit from clinical trials rather than standard of care therapy.

Identifiants

pubmed: 30604000
doi: 10.1007/s10549-018-05106-7
pii: 10.1007/s10549-018-05106-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

443-452

Auteurs

Dilan A Patel (DA)

Washington University School of Medicine, St. Louis, MO, 63110, USA.
Vanderbilt University School of Medicine, Nashville, TN, 37232, USA.

Jing Xi (J)

Washington University School of Medicine, St. Louis, MO, 63110, USA.
St. Luke's Hospital, St. Louis, MO, 63017, USA.

Jingqin Luo (J)

Washington University School of Medicine, St. Louis, MO, 63110, USA.

Bilal Hassan (B)

Washington University School of Medicine, St. Louis, MO, 63110, USA.

Shana Thomas (S)

Washington University School of Medicine, St. Louis, MO, 63110, USA.

Cynthia X Ma (CX)

Washington University School of Medicine, St. Louis, MO, 63110, USA.

Jian L Campian (JL)

Washington University School of Medicine, St. Louis, MO, 63110, USA. campian.jian@wustl.edu.
Division of Oncology, Washington University School of Medicine, Campus Box 8056, 660 South Euclid Ave, St. Louis, MO, 63110, USA. campian.jian@wustl.edu.

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