Adjuvant endocrine therapy is associated with improved overall survival in elderly hormone receptor-positive breast cancer patients.


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:
Nov 2020
Historique:
received: 30 06 2020
accepted: 20 07 2020
pubmed: 11 8 2020
medline: 24 6 2021
entrez: 11 8 2020
Statut: ppublish

Résumé

There is controversy regarding the survival benefit of endocrine therapy (ET) in elderly patients with early invasive hormone receptor-positive (HR+) breast cancer. In this study, we characterize a single institution's practice patterns using adjuvant ET for these patients and evaluated the effect of ET on outcomes. A review of a prospectively maintained database identified 483 women ≥ 70 years old who underwent breast -conserving surgery (BCS) for stage I-III HR+ tumors from 2004-2013. We compared clinicopathologic characteristics, overall survival (OS), disease-free survival (DFS), locoregional recurrence (LRR), and breast cancer-specific survival (BCSS) in patients who did and did not receive ET. Compared to patients who did not get ET, patients who received ET were younger (median age 76 vs 78 years, p = 0.006), had larger tumors (median size 15 vs 14 mm, p = 0.016), underwent sentinel lymph node (LN) biopsy (83.7 vs 67.8%, p < 0.001), had positive LNs (25.5 vs 9.8%, p = 0.008), and received radiation (XRT, 76 vs 43%, p < 0.001). After adjusting for ASA score, age, LN status, tumor grade, and XRT, receipt of ET was associated with improved OS (HR 0.44; 95% CI 0.25-0.77; p = 0.004) and DFS (HR 0.42; 95% CI 0.28-0.64; p < 0.01). Receipt of ET was associated with improved LRR on univariate analysis (HR 0.25; 95% CI 0.09-0.70; p = 0.008); however, after adjusting for grade and XRT, this was not statistically significant on multivariable analysis (HR 0.38; 95% CI 0.13-1.08; p = 0.069) and was not associated with BCSS (HR 0.59; 95% CI 0.16-2.16; p = 0.43). ET was associated with significant improvements in OS and DFS, regardless of clinicopathological features; however, receipt of ET did not impact LRR and BCSS.

Identifiants

pubmed: 32776217
doi: 10.1007/s10549-020-05823-y
pii: 10.1007/s10549-020-05823-y
doi:

Substances chimiques

Hormones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

63-74

Auteurs

Jessica S Crystal (JS)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, 8700 Beverly Blvd, #AC-1046A, Los Angeles, CA, 90048, USA.

Jamie Rand (J)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Department of Surgical Oncology, City of Hope Cancer Center, Duarte, CA, USA.

Jeffrey Johnson (J)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Department of Surgical Oncology, University of North Carolina, Chapel Hill, NC, USA.

Sungjin Kim (S)

Biostatistics and Bioinformatics Research Center, Los Angeles, CA, USA.

Reva Basho (R)

Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, 8700 Beverly Blvd, #AC-1046A, Los Angeles, CA, 90048, USA.

Farin Amersi (F)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, 8700 Beverly Blvd, #AC-1046A, Los Angeles, CA, 90048, USA.

Armando E Giuliano (AE)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, 8700 Beverly Blvd, #AC-1046A, Los Angeles, CA, 90048, USA.

Alice Chung (A)

Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA. alice.chung@cshs.org.
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, 8700 Beverly Blvd, #AC-1046A, Los Angeles, CA, 90048, USA. alice.chung@cshs.org.

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