Adjuvant zoledronic acid and letrozole plus ovarian function suppression in premenopausal breast cancer: HOBOE phase 3 randomised trial

Eur J Cancer. 2019 Sep:118:178-186. doi: 10.1016/j.ejca.2019.05.004. Epub 2019 Jun 1.

Abstract

Aim: The aim of the study is to analyse whether letrozole (L) and zoledronic acid plus L (ZL) are more effective than tamoxifen (T) as adjuvant endocrine treatment of premenopausal patients with breast cancer with hormone receptor-positive (HR+) tumours.

Patients and methods: In a phase 3 trial, 1065 premenopausal patients with HR + early breast cancer received triptorelin to suppress ovarian function and were randomly assigned (1:1:1) to adjuvant T, L or ZL for 5 years. Cancer recurrence, second breast or non-breast cancer and death were considered events for the intention-to-treat disease-free survival (DFS) analysis.

Results: With a 64-month median follow-up and 134 reported events, the disease-free rate at 5 years was 85.4%, 93.2% and 93.3% with T, L and ZL, respectively (overall P = 0.008). The hazard ratio for a DFS event was 0.52 (95% confidence interval [CI], 0.34 to 0.80; P = 0.003) with ZL vs T, 0.72 (95% CI, 0.48 to 1.07; P = 0.06) with L vs T and 0.70 (95% CI, 0.44 to 1.12; P = 0.22) with ZL vs L. With 36 deaths, there was no significant difference in overall survival (P = 0.14). Treatment was stopped for toxicity or refusal in 7.3%, 7.3% and 16.6% patients, and in the safety population, grade 3-4 side-effects were reported in 4.2%, 6.9% and 9.1% patients treated with T, L or ZL, respectively.

Conclusion: HOBOE study shows that in premenopausal patients with early breast cancer undergoing ovarian function suppression with triptorelin, ZL significantly improves DFS, while worsening compliance and toxicity, as compared with T. (NCT00412022).

Keywords: Adjuvant endocrine treatment; Aromatase inhibitors; Breast cancer; Phase 3; Premenopausal patients; Zoledronic acid.

Publication types

  • Clinical Trial, Phase III
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Aromatase Inhibitors / adverse effects
  • Aromatase Inhibitors / therapeutic use*
  • Bone Density Conservation Agents / adverse effects
  • Bone Density Conservation Agents / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / physiopathology
  • Chemotherapy, Adjuvant
  • Disease Progression
  • Disease-Free Survival
  • Estrogen Antagonists / adverse effects
  • Estrogen Antagonists / therapeutic use*
  • Female
  • Humans
  • Italy
  • Letrozole / adverse effects
  • Letrozole / therapeutic use*
  • Middle Aged
  • Ovary / drug effects*
  • Ovary / physiopathology
  • Premenopause*
  • Tamoxifen / adverse effects
  • Tamoxifen / therapeutic use*
  • Time Factors
  • Triptorelin Pamoate / adverse effects
  • Triptorelin Pamoate / therapeutic use*
  • Zoledronic Acid / adverse effects
  • Zoledronic Acid / therapeutic use*

Substances

  • Aromatase Inhibitors
  • Bone Density Conservation Agents
  • Estrogen Antagonists
  • Triptorelin Pamoate
  • Tamoxifen
  • Zoledronic Acid
  • Letrozole

Associated data

  • ClinicalTrials.gov/NCT00412022