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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

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

11 Citas (Scopus)

Resumen

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.

Idioma originalInglés
Páginas (desde-hasta)959-967
Número de páginas9
PublicaciónBritish Journal of Cancer
Volumen120
N.º10
DOI
EstadoPublicada - 14 may. 2019
Publicado de forma externa

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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