4.3 Article

Beta-2 Adrenergic Receptor Gene Expression in HER2-Positive Early-Stage Breast Cancer Patients: A Post-hoc Analysis of the NCCTG-N9831 (Alliance) Trial

Journal

CLINICAL BREAST CANCER
Volume 22, Issue 4, Pages 308-318

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.clbc.2021.11.012

Keywords

Breast cancer; HER2; Beta-2 adrenergic receptor; ADRB2; Trastuzumab

Categories

Funding

  1. National Cancer Institute of the National Institutes of Health [U10CA180821, U10CA180882, U24CA196171]
  2. Genentech
  3. Genomic Health
  4. Breast Cancer Research Foundation
  5. Fondation Cancer Luxem-bourg

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In this post-hoc analysis of the NCCTG-N9831 trial, a high expression of the beta 2AR gene (ADRB2) was associated with longer disease-free survival and identified patients who benefited from adjuvant trastuzumab in HER2-positive breast cancer.
Beta-2 adrenergic receptor (beta 2AR) modulates T-cell activation and previous studies have associated a high expression of the beta 2AR gene (ADRB2) with a favorable prognosis in HER2-positive breast cancer patients. In this post-hoc analysis of the NCCTG-N9831 trial, a high ADRB2 expression was associated with longer disease-free survival and also identified patients who benefited from adjuvant trastuzumab. Background: Beta-2 adrenergic receptor (beta 2AR) modulates immune activation and may enhance trastuzumab activity. We assessed the impact of beta 2AR gene (ADRB2) expression on the outcomes of patients with HER2-positive early-stage breast cancer enrolled on the NCCTG-N9831 trial. Patients and Methods: This is a post-hoc analysis of the NCCTG-N9831 trial, which compared chemotherapy (arm A) versus chemotherapy plus trastuzumab (arms B&C) as adjuvant treatment of patients with HER2-positive early-stage breast cancer, with disease-free survival (DFS) as primary endpoint. Gene expression levels retrieved by DASL assay were used to classify patients as ADRB2-high or ADRB2-low. Hazard ratios (HRs) were calculated by a Cox proportional model adjusted for prognostic variables and ADRB2 expression. Correlations between ADRB2 expression and stromal tumor-infiltrating lymphocyte (TIL) levels were assessed with Pearson coefficient. A multivariable Cox regression model with interaction term was performed to assess the interaction between ADRB2 expression and treatment arm; and ADRB2 expression and a 8-gene signature previously shown to predict trastuzumab benefit. Results: Overall, 1,282 patients were included (ADRB2-high [N = 944] / ADRB2-low [N = 338]). A high expression of ADRB2 was associated with a longer DFS (P = .01) in the overall population. The addition of trastuzumab to chemotherapy improved DFS only in patients with ADRB2-high tumors (P < .01). ADRB2 expression was correlated with TIL levels (r = 0.24, P < .001). No association between ADRB2 expression and the 8-gene trastuzumab benefit signature was observed (P = .32). Conclusion: Our findings suggest that a high ADRB2 expression is a favorable prognostic factor and may identify patients with HER2-positive early-stage breast cancer who benefit from adjuvant trastuzumab. (C) 2021 Elsevier Inc. All rights reserved.

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