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Polychemotherapy for early breast cancer: An overview of the randomised trials

  • Early Breast Cancer Trialists' Collaborative Group (EBCTCG)
  • 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
  • Centre Georges-François Leclerc
  • Université libre de Bruxelles
  • Dana-Farber Cancer Institute
  • Bradford Teaching Hospitals NHS Foundation Trust
  • BC Cancer
  • Caen Centre Regional Francois Baclesse
  • Cambridge University Hospitals NHS Foundation Trust
  • Cancer and Leukemia Group B
  • Memorial Sloan-Kettering Cancer Center
  • International Breast Cancer Study Group (Ludwig)
  • Cancer Research UK
  • Nolvadex Adjuvant Trial Organisation
  • University of Cape Town
  • SASIB International Trialists
  • 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-Western British Surgeons
  • Portuguese Oncology Institute
  • Danish Health Authority
  • Copenhagen Radium Centre
  • Cracow Institute of Oncology
  • CRCRAMS
  • Danish Breast Cancer Cooperative Group
  • St Lukes Hospital
  • Heinrich Heine University Düsseldorf
  • Eastern Cooperative Oncology Group
  • University of Oxford
  • Edinburgh Breast Unit
  • Elim Hospital
  • European Organisation for Research and Treatment of Cancer Data Center
  • Leiden University
  • Evanston Northwestern Healthcare
  • GFEA
  • GBSG (BMFT)
  • Ghent University
  • GIVIO Interdisciplinary Group for Cancer Care Evaluation
  • 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
  • University of Innsbruck
  • Swiss Group for Clinical Cancer Research
  • Charing Cross Hospital
  • 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
  • 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 Cancer Institute of Canada Clinical Trials Group
  • Toronto-Edmonton Breast Cancer Study Group
  • Princess Margaret Cancer Centre
  • NSABP Foundation, Inc.
  • North Sweden Breast Cancer Group
  • 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
  • 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
  • Fox Chase Cancer Center
  • Piedmont Oncology Association
  • Charles University
  • University of Pretoria
  • Instituto Cardiovascular de Rosario
  • Erasmus University Rotterdam
  • Royal Marsden NHS Foundation Trust
  • St George’s Hospital
  • Russian Ministry of Health
  • Sardinia Oncology Hospital A Businico
  • Saskatchewan Cancer Agency
  • Scottish Cancer Therapy Network
  • 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. There have been many randomised trials of adjuvant prolonged polychemotherapy among women with early breast cancer, and an updated overview of their results is presented. Methods. In 1995, information was sought on each woman in any randomised trial that began before 1990 and involved treatment groups that differed only with respect to the chemotherapy regimens that were being compared. Analyses involved about 18,000 women in 47 trials of prolonged polychemotherapy versus no chemotherapy, about 6000 in 11 trials of longer versus shorter polychemotherapy, and about 6000 in 11 trials of anthracycline-containing regimens versus CMF (cyclophosphamide, methotrexate, and fluorouracil). Findings. For recurrence, polychemotherapy produced substantial and highly significant proportional reductions both among women aged under 50 at randomisation (35% [SD 4] reduction; 2p < 0.00001) and among those aged 50-69 (20% [SD 3] reduction; 2p < 0.00001); few women aged 70 or over had been studied. For mortality, the reductions were also significant both among women aged under 50 (27% [SD 5] reduction; 2p < 0.00001) and among those aged 50-69 (11% [SD 3] reduction; 2p = 0.0001). The recurrence reductions emerged chiefly during the first 5 years of follow-up, whereas the difference in survival grew throughout the first 10 years. After standardisation for age and time since randomisation, the proportional reductions in risk were similar for women with node-negative and node positive disease. Applying the proportional mortality reduction observed in all women aged under 50 at randomisation would typically change a 10-year survival of 71% for those with node-negative disease to 78% (an absolute benefit of 7%), and of 42% for those with node positive disease to 53% (an absolute benefit of 11%). The smaller proportional mortality reduction observed in all women aged 50-69 at randomisation would translate into smaller absolute benefits, changing a 10-year survival of 67% for those with node-negative disease to 69% (an absolute gain of 2%) and of 46% for those with node-positive disease to 49% (an absolute gain of 3%). The age-specific benefits of polychemotherapy appeared to be largely irrespective of menopausal status at presentation, oestrogen receptor status of the primary tumour, and of whether adjuvant tamoxifen had been given. In terms of other outcomes, there was a reduction of about one-fifth (2p = 0.05) in contralateral breast cancer, which has already been included in the analyses of recurrence, and no apparent adverse effect on deaths from causes other than breast cancer (death rate ratio 0.89 [SD 0.09]). The directly randomised comparisons of longer versus shorter durations of polychemotherapy did not indicate any survival advantage with the use of more than about 3-6 months of polychemotherapy. By contrast, directly randomised comparisons did suggest that, compared with CMF alone, the anthracycline-containing regimens studied produced somewhat greater effects on recurrence (2p = 0.006) and mortality (69% vs 72% 5-year survival; log-rank 2p = 0.02). But this comparison is one of many that could have been selected for emphasis, the 99% CI reaches zero, and the results of several of the relevant trials are not yet available. Interpretation. Some months of adjuvant polychemotherapy (eg, with CMF or an anthracycline-containing regimen) typically produces an absolute improvement of about 7-11% in 10-year survival for women aged under 50 at presentation with early breast cancer, and of about 2-3% for those aged 50-69 (unless their prognosis is likely to be extremely good even without such treatment). Treatment decisions involve consideration not only of improvements in cancer recurrence and survival but also of adverse side-effects of treatment, and this report makes no recommendations as to who should or should not be treated.

Original languageEnglish
Pages (from-to)930-942
Number of pages13
JournalLancet
Volume352
Issue number9132
DOIs
Publication statusPublished - 19 Sept 1998
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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