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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.
Ribi, Karin; Luo, Weixiu; Colleoni, Marco; Karlsson, Per; Chirgwin, Jacquie; Aebi, Stefan; Jerusalem, Guy; Neven, Patrick; Di Lauro, Vincenzo; Gomez, Henry L; Ruhstaller, Thomas; Abdi, Ehtesham; Biganzoli, Laura; Müller, Bettina; Barbeaux, Annelore; Graas, Marie-Pascale; Rabaglio, Manuela; Francis, Prudence A; Foukakis, Theodoros; Pagani, Olivia; Graiff, Claudio; Vorobiof, Daniel; Maibach, Rudolf; Di Leo, Angelo; Gelber, Richard D; Goldhirsch, Aron; Coates, Alan S; Regan, Meredith M; Bernhard, Jürg.
Afiliação
  • Ribi K; Quality of Life Office, International Breast Cancer Study Group Coordinating Center, Bern, Switzerland.
  • Luo W; International Breast Cancer Study Group Statistical Center, Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Colleoni M; Division of Medical Senology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
  • Karlsson P; Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy/Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.
  • Chirgwin J; Box Hill and Maroondah Hospitals, Monash University, Victoria, Australia.
  • Aebi S; Luzerner Kantonsspital, Lucerne, Switzerland.
  • Jerusalem G; CHU Liège, Liège University, Liège, Belgium.
  • Neven P; Multidisciplinary Breast Center, University Hospitals, KU Leuven, Leuven, Belgium.
  • Di Lauro V; Division of Medical Oncology B, CRO-Aviano, Aviano, Italy.
  • Gomez HL; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Ruhstaller T; Breast Center St. Gallen, Swiss Group for Clinical Cancer Research and International Breast Cancer Study Group, Bern, Switzerland.
  • Abdi E; The Tweed Hospital, Tweed Heads, NSW & Griffith University Gold Coast, Southport, Australia.
  • Biganzoli L; Hospital of Prato-AUSL Toscana Centro, Istituto Toscano Tumori, Prato, Italy.
  • Müller B; Chilean Cooperative Group for Oncologic Research (GOCCHI), Providencia, Santiago, Chile.
  • Barbeaux A; CHR Verviers, Verviers, Belgium.
  • Graas MP; CHC Clinique St. Joseph, Liège, Belgium.
  • Rabaglio M; Bern University Hospital, Inselspital, Bern, Switzerland.
  • Francis PA; Peter MacCallum Cancer Center, University of Melbourne, Melbourne and Breast Cancer Trials Australia & New Zealand, University of Newcastle, Newcastle, Australia.
  • Foukakis T; Department of Oncology, Karolinska Institute and University Hospital, Stockholm, Sweden.
  • Pagani O; Institute of Oncology of Southern Switzerland, Bellinzona, Geneva University Hospitals, Geneva, Swiss Group for Clinical Cancer Research (SAKK) and International Breast Cancer Study Group, Bern, Switzerland.
  • Graiff C; Division of Medical Oncology, Ospedale Centrale di Bolzano, Bolzano, Italy.
  • Vorobiof D; Sandton Oncology Centre, Johannesburg, South Africa.
  • Maibach R; International Breast Cancer Study Group Coordinating Center, Bern, Switzerland.
  • Di Leo A; Hospital of Prato-AUSL Toscana Centro, Istituto Toscano Tumori, Prato, Italy.
  • Gelber RD; International Breast Cancer Study Group Statistical Center, Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Harvard T.H. Chan School of Public Health and Frontier Science and Technology Research Foundation, Boston, MA, USA.
  • Goldhirsch A; International Breast Cancer Study Group and IEO, European Institute of Oncology IRCCS, Milan, Italy.
  • Coates AS; International Breast Cancer Study Group and University of Sydney, Sydney, Australia.
  • Regan MM; International Breast Cancer Study Group Statistical Center, Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
  • Bernhard J; Quality of Life Office, International Breast Cancer Study Group Coordinating Center and Bern University Hospital, Inselspital, Bern, Switzerland. juerg.bernhard@ibcsg.org.
Br J Cancer ; 120(10): 959-967, 2019 05.
Article em En | MEDLINE | ID: mdl-30967649
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Quimioterapia Adjuvante / Letrozol / Linfonodos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Quimioterapia Adjuvante / Letrozol / Linfonodos Idioma: En Ano de publicação: 2019 Tipo de documento: Article