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Ovarian ablation in early breast cancer: Overview of the randomised trials

  • Early Breast Cancer Trialists' Collaborative Group
  • ACETBC
  • National Cancer Center Japan
  • Integraal Kankercentrum
  • Metaxa Cancer Hospital
  • Auckland Breast Cancer Study Group
  • Australian-New Zealand Breast Cancer Trials Group
  • Belgian Adjuvant Breast Cancer Project
  • Berlin-Brandenburg Academy of Sciences and Humanities
  • Birmingham General Hospital
  • BMFT Freiberg
  • Centre Georges-François Leclerc
  • Bordet Institute
  • Dana-Farber Cancer Institute
  • Cancer and Leukemia Group B
  • Bradford Teaching Hospitals NHS Foundation Trust
  • BC Cancer
  • Caen Centre Regional Francois Baclesse
  • International Breast Cancer Study Group (Ludwig)
  • Cambridge University Hospitals NHS Foundation Trust
  • Cancer Research UK
  • Nolvadex Adjuvant Trial Organisation
  • University of Cape Town
  • SASIB International Trialists
  • Cardiff Surgery Trialists
  • Scottish Cancer Trials Office
  • Case Western Reserve University
  • Central Oncology Group
  • Centre Léon Bérard
  • Gloucestershire Hospitals NHS Foundation Trust
  • The University of Chicago
  • The Christie NHS Foundation Trust
  • North Sweden Breast Cancer Group
  • North-Western British Surgeons
  • Portuguese Oncology Institute
  • Danish Health Authority
  • Copenhagen Radium Centre
  • Cracow Institute of Oncology
  • Danish Breast Cancer Cooperative Group
  • St Lukes Hospital
  • Heinrich Heine University Düsseldorf
  • Eastern Cooperative Oncology Group
  • University of Oxford
  • Elim Hospital
  • European Organization for Research and Treatment of Cancer
  • Evanston Northwestern Healthcare
  • Ghent University
  • Beatson Oncology Centre
  • Victoria Infirmary
  • University of Granada
  • Gruppo Ricerca Ormono Chemio Terapia Adiuvante
  • Guadalajara Hospital de 20 Noviembre
  • Gunma University
  • King's College London
  • Gynecological Adjuvant Breast Group
  • Heidelberg University 
  • Hellenic Cooperative Oncology Group
  • Helsinki Deaconess Medical Centre
  • University of Helsinki
  • ICRF
  • University of Innsbruck
  • Swiss Group for Clinical Cancer Research
  • International Collaborative Cancer Group
  • Israel NSABC
  • Italian Cooperative Chemo-RadioSurgical Group
  • Japanese National Hospitals Group Breast Cancer Study Group
  • Kawasaki Medical School
  • Kumamoto University
  • Breast Cancer Study Group of the Comprehensive Cancer Centre
  • Louvain Academisch Ziekenhuis St Rafael
  • Lund University
  • Marseille Laboratoire de Cancerologie Biologique APM
  • Mayo Clinic Rochester, MN
  • University of Texas MD Anderson Cancer Center
  • Memorial Sloan-Kettering Cancer Center
  • Mexican National Medical Centre
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • Montpellier Centre Paul Lamarque
  • University of Naples Federico II
  • National Institutes of Health
  • National Surgical Adjuvant Project for Breast & Bowel Cancers
  • Northwick Park Hospital
  • Norwegian Breast Cancer Group
  • University of Oslo
  • Scandinavian Adjuvant Chemotherapy Study Group
  • City Hospital
  • Oita Prefectural Hospital
  • Oncofrance
  • Ontario Cancer Treatment & Research Foundation
  • Ontario Clinical Oncology Group
  • Canadian Cancer Trials Group
  • Toronto-Edmonton Breast Cancer Study Group
  • Princess Margaret Cancer Centre
  • Osaka Metropolitan University
  • National Hospital Organization Osaka National Hospital
  • Oxford University Hospitals NHS Foundation Trust
  • Centre René Huguenin
  • Institut Curie
  • Gustave Roussy Comprehensive Cancer Institute
  • Parma Hospital
  • Philadelphia Fox Chase Cancer Centre
  • Piedmont Oncology Association
  • Charles University
  • University of Pretoria
  • Instituto Cardiovascular de Rosario
  • Erasmus University Rotterdam
  • Institute of Cancer Research
  • St George’s Hospital
  • Russian Ministry of Health
  • Sardinia Oncology Hospital A Businico
  • Saskatchewan Cancer Agency
  • South Swedish Breast Cancer Group
  • South-East Sweden Breast Cancer Group
  • Southeastern Cancer Study Group & Alabama Breast Cancer Project
  • Southwest Oncology Group
  • Stockholm Breast Cancer Study Group
  • Karolinska Institutet
  • Tel Aviv University
  • Japanese Foundation for Cancer Research
  • Institut Claudius Regaud
  • Université de Tunis El Manar
  • UK Multicentre Cancer Chemotherapy Study Group
  • UK/Asia Collaborative Breast Cancer Group
  • Uppsala-Orebro Cancer Study Group
  • University of Vienna
  • Wessex Radiotherapy Centre
  • West Midlands Oncology Association
  • West of Scotland Breast Trial Group
  • Western Cancer Study Group
  • University of the Witwatersrand
  • University of Würzburg

Research output: Contribution to journalArticlepeer-review

Abstract

Background. Among women with early breast cancer, the effects of ovarian ablation on recurrence and death have been assessed by several randomised trials that now have long follow-up. In this report, the Early Breast Cancer Trialists' Collaborative Group present their third and yearly systematic overview (meta-analysis), now with 15 years' follow-up. Methods. In 1995, information was sought on each patient in any randomised trial of ovarian ablation or suppression versus control that began before 1990. Data were obtained for 12 of the 13 studies that assessed ovarian ablation by irradiation or surgery, all of which began before 1980, but not for the four studies that assessed ovarian suppression by drugs, all of which began after 1985. Menopausal status was not consistently defined across trials; therefore, the main analyses are limited to women aged under 50 (rather than 'premenopausal') when randomised. Oestrogen receptors were measured only in the trials of ablation plus cytotoxic chemotherapy versus the same chemotherapy alone. Findings. Among 2102 women aged under 50 when randomised, most of whom would have been premenopausal at diagnosis, 1130 deaths and an additional 153 recurrences were reported. 15-year survival was highly significantly improved among those allocated ovarian ablation (52.4 vs 46.1%, 6.3 [SD 2.3] fewer deaths per 100 women, logrank 2p = 0.001), as was recurrence-free survival (45.0 vs 39.0%, 2p = 0.0007). The numbers of events were too small for any subgroup analyses to be reliable. The benefit was, however, significant both for those with ('node positive') and for those without ('node negative') axillary spread when diagnosed. In the trials of ablation plus cytotoxic chemotherapy versus the same chemotherapy alone, the benefit appeared smaller (even for women with oestrogen receptors detected on the primary tumour) than in the trials of ablation in the absence of chemotherapy (where the observed survival improvements were about six per 100 node-negative women and 12 per 100 node-positive women). Among 1354 women aged 50 or over when randomised, most of whom would have been perimenopausal or postmenopausal, there was only a nonsignificant improvement in survival and recurrence-free survival. Interpretation. In women aged under 50 with early breast cancer, ablation of functioning ovaries significantly improves long-term survival, at least in the absence of chemotherapy. Further randomised evidence is needed on the additional effects of ovarian ablation in the presence of other adjuvant treatments, and to assess the relevance of hormone-receptor measurements.

Original languageEnglish
Pages (from-to)1189-1196
Number of pages8
JournalLancet
Volume348
Issue number9036
DOIs
Publication statusPublished - 1996
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

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