Skip to main navigation Skip to search Skip to main content

Quality of life under extended continuous versus intermittent adjuvant letrozole in lymph node-positive, early breast cancer patients: the SOLE randomised phase 3 trial

  • on behalf of the SOLE Investigators
  • International Breast Cancer Study Group Coordinating Center
  • Dana-Farber Cancer Institute
  • European Institute of Oncology
  • Sahlgrenska University Hospital
  • Monash University
  • Luzerner Kantonsspital
  • University Hospital of Liège
  • University Hospital Gasthuisberg
  • IRCCS Centro Di Riferimento Oncologico Aviano
  • Instituto Nacional de Enfermedades Neoplásicas Eduardo Cáceres Graziani
  • Swiss Group for Clinical Cancer Research
  • Griffith University
  • Prevention and Clinical Network (ISPRO)
  • Chilean Cooperative Group for Oncologic Research (GOCCHI)
  • CHR Verviers
  • CHC Clinique St. Joseph
  • University of Bern
  • University of Melbourne
  • Karolinska Institutet
  • University of Geneva and Geneva University Hospitals
  • Ospedale Centrale di Bolzano
  • Sandton Oncology Centre
  • Harvard Medical School
  • University of Sydney

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Background: In the phase III SOLE trial, the extended use of intermittent versus continuous letrozole for 5 years did not improve disease-free survival in postmenopausal women with hormone receptor-positive breast cancer. Intermittent therapy with 3-month breaks may be beneficial for patients’ quality of life (QoL). Methods: In the SOLE QoL sub-study, 956 patients completed the Breast Cancer Prevention Trial (BCPT) symptom and further QoL scales up to 24 months after randomisation. Differences in change of QoL from baseline between the two administration schedules were tested at 12 and 24 months using repeated measures mixed-models. The primary outcome was change in hot flushes at 12 months. Results: There was no difference in hot flushes at 12 months between the two schedules, but patients receiving intermittent letrozole reported significantly more improvement at 24 months. They also indicated less worsening in vaginal problems, musculoskeletal pain, sleep disturbance, physical well-being and mood at 12 months. Overall, 25–30% of patients reported a clinically relevant worsening in key symptoms and global QoL. Conclusion: Less symptom worsening was observed during the first year of extended treatment with the intermittent administration. For women experiencing an increased symptom burden of extended adjuvant endocrine therapy, an intermittent administration is a safe alternative. Clinical trial information: Clinical trial information: NCT00651456.

Original languageEnglish
Pages (from-to)959-967
Number of pages9
JournalBritish Journal of Cancer
Volume120
Issue number10
DOIs
StatePublished - 14 May 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Quality of life under extended continuous versus intermittent adjuvant letrozole in lymph node-positive, early breast cancer patients: the SOLE randomised phase 3 trial'. Together they form a unique fingerprint.

Cite this