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Ten-year update: NRG Oncology/National Surgical Adjuvant Breast and Bowel Project B-42 randomized trial: extended letrozole therapy in early-stage breast cancer.
Mamounas, Eleftherios P; Bandos, Hanna; Rastogi, Priya; Lembersky, Barry C; Jeong, Jong-Hyeon; Geyer, Charles E; Fehrenbacher, Louis; Chia, Stephen K; Brufsky, Adam M; Walshe, Janice M; Soori, Gamini S; Dakhil, Shaker R; Wade, James L; McCarron, Edward C; Swain, Sandra M; Wolmark, Norman.
Affiliation
  • Mamounas EP; Department of Surgical Oncology, Orlando Health Cancer Institute, Orlando, FL, USA.
  • Bandos H; NRG Oncology SDMC, and the Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA.
  • Rastogi P; University of Pittsburgh Medical Center Hillman Cancer Center, Department of Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Lembersky BC; Department of Oncology, University of Pittsburgh Magee-Womens Hospital, Pittsburgh, PA, USA.
  • Jeong JH; University of Pittsburgh Medical Center Hillman Cancer Center, Department of Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Geyer CE; NRG Oncology SDMC, and the Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA.
  • Fehrenbacher L; University of Pittsburgh Medical Center Hillman Cancer Center, Department of Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Chia SK; Department of Medical Oncology, Kaiser Permanente Oncology Clinical Trials Northern California, Novato, CA, USA.
  • Brufsky AM; Department of Medical Oncology, British Columbia Cancer Agency (BCCA), Vancouver, British Columbia, Canada.
  • Walshe JM; Department of Oncology, University of Pittsburgh Magee-Womens Hospital, Pittsburgh, PA, USA.
  • Soori GS; Department of Oncology, Cancer Trials Ireland (formerly known as Irish Clinical Oncology Research Group-ICORG), Dublin, Ireland.
  • Dakhil SR; Department of Oncology, Florida Cancer Specialists, Fort Myers, FL, USA.
  • Wade JL; Department of Oncology, Community Clinical Oncology Program, Wichita via Christi Regional Medical Center, Wichita, KS, USA.
  • McCarron EC; Department of Oncology, Decatur Memorial Hospital, Cancer Care Specialists of Illinois, Heartland National Cancer Institute Community Oncology Research Program, Decatur, IL, USA.
  • Swain SM; Department of Surgical Oncology, MedStar Franklin Square Medical Center at Weinberg Cancer Institute, Baltimore, MD, USA.
  • Wolmark N; Department of Surgical Oncology, Georgetown Lombardi Comprehensive Cancer Center, MedStar Health, Washington, DC, USA.
J Natl Cancer Inst ; 115(11): 1302-1309, 2023 11 08.
Article in En | MEDLINE | ID: mdl-37184928
ABSTRACT

BACKGROUND:

The National Surgical Adjuvant Breast and Bowel Project B-42 trial evaluated extended letrozole therapy (ELT) in postmenopausal breast cancer patients who were disease free after 5 years of aromatase inhibitor (AI)-based therapy. Seven-year results demonstrated a nonstatistically significant trend in disease-free survival (DFS) in favor of ELT. We present 10-year outcome results.

METHODS:

In this double-blind, phase III trial, patients with stage I-IIIA hormone receptor-positive breast cancer, disease free after 5 years of an AI or tamoxifen followed by an AI, were randomly assigned to 5 years of letrozole or placebo. Primary endpoint was DFS, defined as time from random assignment to breast cancer recurrence, second primary malignancy, or death. All statistical tests are 2-sided.

RESULTS:

Between September 2006 and January 2010, 3966 patients were randomly assigned (letrozole 1983; placebo 1983). Median follow-up time for 3923 patients included in efficacy analyses was 10.3 years. There was statistically significant improvement in DFS in favor of letrozole compared with placebo (hazard ratio [HR] = 0.85, 95% confidence interval [CI] = 0.74 to 0.96; P = .01; 10-year DFS placebo = 72.6%, letrozole = 75.9%, absolute difference = 3.3%). There was no difference in the effect of letrozole on overall survival (HR = 0.97, 95% CI = 0.82 to 1.15; P = .74). Letrozole statistically significantly reduced breast cancer-free interval events (HR = 0.75, 95% CI = 0.62 to 0.91; P = .003; absolute difference in cumulative incidence = 2.7%) and distant recurrences (HR = 0.72, 95% CI = 0.55 to 0.92; P = .01; absolute difference = 1.8%). The rates of osteoporotic fractures and arterial thrombotic events did not differ between treatment groups.

CONCLUSIONS:

The beneficial effect of ELT on DFS persisted at 10 years. Letrozole also improved breast cancer-free interval and distant recurrences without improving overall survival. Careful assessment of potential risks and benefits is necessary for selecting appropriate candidates for ELT.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Clinical_trials Limits: Female / Humans Language: En Journal: J Natl Cancer Inst Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Clinical_trials Limits: Female / Humans Language: En Journal: J Natl Cancer Inst Year: 2023 Type: Article Affiliation country: United States