Skip to main content

Primary Endocrine Therapy vs Upfront Surgery for Older Women With Estrogen Receptor-Positive Breast Cancer: A Systematic Review and Meta-Analysis

In brief

Endocrine therapy showed no significant survival difference from surgery in older women

In a review of 29 studies involving 22,821 patients, randomized trials found no statistically significant overall survival difference between primary endocrine therapy and upfront surgery, although results leaned toward surgery. Disease control on endocrine therapy lasted longer in studies selecting patients by tumor biology, suggesting that biology and frailty - not age alone - should guide who might be a candidate.

Journal
JAMA network open (Q1)
Published
2 November 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Neil Carleton, Jian Zou, Yangyang Mu, Steffi Oesterreich, Shannon Puhalla, Julia Foldi, et al.
PMID
42993545
DOI
10.1001/jamanetworkopen.2026.43218

Why clinicians should know about it

  • Picked for Breast and Endocrine Surgery (paper of the day, 7 November 2026): Direct comparison of endocrine therapy and surgery for operable breast
  • Picked for Surgical Oncology (paper of the day, 7 November 2026): Primary endocrine therapy vs upfront surgery for older women with

Abstract

IMPORTANCE: As the population of older women with breast cancer grows, an increasing number are considered for primary endocrine therapy (pET), yet clinicians lack a framework for identifying which patients are appropriate candidates, resulting in reliance on chronologic age and life expectancy rather than tumor biology. OBJECTIVE: To evaluate survival and variables associated with response duration for patients treated with pET. DATA SOURCES: PubMed, MEDLINE, Web of Science, and Cochrane Central Register of Controlled Trials were searched from inception through March 26, 2026. STUDY SELECTION: Randomized clinical trials (RCTs) and non-RCT (observational) cohorts comparing pET with surgery in operable, nonmetastatic, estrogen receptor (ER)-positive breast cancer. DATA EXTRACTION AND SYNTHESIS: Data were extracted independently by 2 reviewers per Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Hazard ratios (HRs) not directly reported were reconstructed from Kaplan-Meier curves. Randomized clinical trial-derived HRs for overall survival (OS) and breast cancer-specific survival (BCSS) were pooled using a random-effects model, given anticipated heterogeneity across trials spanning 5 decades and differing tumor biology criteria. Observational cohorts were analyzed descriptively, not pooled for comparative survival, given susceptibility to confounding by indication. MAIN OUTCOMES AND MEASURES: The main outcomes were OS and BCSS (RCTs) assessed using meta-analysis. Time to progression, salvage intervention rates, and variables associated with progression and mortality (observational cohorts) were assessed using descriptive analyses. RESULTS: Twenty-nine studies (6 RCTs and 23 observational cohorts; 22 821 patients; overall median [IQR] age, 83.1 [77.0-85.0] years) met the inclusion criteria. Patients from RCTs were generally younger (median [IQR] age, 77.0 [75.8-78.0] years) than those from the observational studies (median [IQR] age, 84.0 [81.5-86.0] years). Treatment with pET was not associated with a statistically significant OS difference vs surgery (HR, 1.14; 95% CI, 0.98-1.33), though the point estimate favored surgery. Median time to progression ranged from 19.7 months (range, 13.5-26.0 months) in tumor biology-unselected, tamoxifen-era cohorts to more than 50 months in ER-selected and aromatase inhibitor-treated cohorts. Tumor biology was consistently associated with progression risk. CONCLUSIONS AND RELEVANCE: This systematic review and meta-analysis of more than 22 000 patients with ER-positive breast cancer found no statistically significant survival difference between pET and upfront surgery. Durable disease control under pET seemed to be concentrated in patients with favorable biology. These findings support a framework incorporating tumor biology and frailty, rather than age alone, to identify candidates for pET.

Abstract as published, via PubMed.

View on PubMedFull text at the publisherOpen in the app

For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.