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Be Part of Research - Trial Details - Combination Chemotherapy in Treating Women With Breast Cancer Who Have Undergone Surgery

Combination Chemotherapy in Treating Women With Breast Cancer Who Have Undergone Surgery

Medical Conditions

Breast Neoplasms


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which chemotherapy regimen is more effective in treating women after surgery for breast cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of paclitaxel, epirubicin, and cyclophosphamide with or without gemcitabine in treating women who have undergone surgery for breast cancer.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Aug 2001 Aug 2001

Publications

"Earl HM, Hiller L, Howard HC, Dunn JA, Young J, Bowden SJ, McDermaid M, Waterhouse AK, Wilson G, Agrawal R, O'Reilly S, Bowman A, Ritchie DM, Goodman A, Hickish T, McAdam K, Cameron D, Dodwell D, Rea DW, Caldas C, Provenzano E, Abraham JE, Canney P, Crown JP, Kennedy MJ, Coleman R, Leonard RC, Carmichael JA, Wardley AM, Poole CJ; tAnGo trial collaborators. Addition of gemcitabine to paclitaxel, epirubicin, and cyclophosphamide adjuvant chemotherapy for women with early-stage breast cancer (tAnGo): final 10-year follow-up of an open-label, randomised, phase 3 trial. Lancet Oncol. 2017 Jun;18(6):755-769. doi: 10.1016/S1470-2045(17)30319-4. Epub 2017 May 4."; "28479233"

INTERVENTIONAL

Intervention Type : DRUG

Intervention Type : DRUG

Intervention Type : DRUG

Intervention Type : DRUG

Intervention Type : PROCEDURE



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Beatson Oncology Centre
    Glasgow
    Scotland
    G11 6NT
  • Walsgrave Hospital
    Coventry
    England
    CV2 2DX
  • Leeds Cancer Centre at St. James's University Hospital
    Leeds
    England
    LS9 7TF
  • Cancer Research Centre at Weston Park Hospital
    Sheffield
    England
    S1O 2SJ
  • St. George's Hospital
    London
    England
    SW17 0QT
  • Northern Centre for Cancer Treatment at Newcastle General Hospital
    Newcastle-Upon-Tyne
    England
    NE4 6BE
  • Nottingham City Hospital NHS Trust
    Nottingham
    England
    NG5 1PB
  • James Cook University Hospital
    Middlesbrough
    England
    TS4 3BW
  • Hinchingbrooke Hospital
    Huntingdon
    England
    PE18 6NT
  • Derriford Hospital
    Plymouth
    England
    PL6 8DH
  • Peterborough Hospitals Trust
    Peterborough
    England
    PE3 6DA
  • Clatterbridge Centre for Oncology NHS Trust
    Merseyside
    England
    L63 4JY
  • Walsall Manor Hospital
    Walsall
    England
    WS2 9PS
  • Christie Hospital N.H.S. Trust
    Manchester
    England
    M20 4BX
  • Oldchurch Hospital
    Romford
    England
    RM7 OBE
  • Royal Shrewsbury Hospital
    Shrewsbury
    England
  • Torbay Hospital
    Torquay Devon
    England
    TQ2 7AA
  • Cookridge Hospital at Leeds Teaching Hospital NHS Trust
    Leeds
    England
    LS16 6QB
  • Dorset County Hospital
    Dorchester
    England
    DT1 2JY
  • Addenbrooke's Hospital at Cambridge University Hospitals NHS Foundation Trust
    Cambridge
    England
    CB2 2QQ
  • Essex County Hospital
    Colchester
    England
    C03 3NB
  • Sandwell General Hospital
    West Bromwich
    England
    B71 4HJ
  • Good Hope Hospital Trust
    West Midlands
    England
    B75 7RR
  • City Hospital - Birmingham
    Birmingham
    England
    B18 7QH
  • Crosshouse Hospital
    Kilmarnock
    England
    KA2 OBE
  • Royal Infirmary - Castle
    Glasgow
    Scotland
    G4 0SF
  • King George Hospital
    Ilford, Essex
    England
    IG3 8YB
  • Cancer Research UK Clinical Trials Unit - Birmingham
    Birmingham
    England
    B15 2TT
  • Princess Royal Hospital
    Hull
    England
    HU8 9HE
  • Queen Elizabeth Hospital
    King's Lynn
    PE30 4ET
  • Queen Elizabeth Hospital at University of Birmingham
    Birmingham
    England
    B15 2TH
  • Birmingham Heartlands and Solihull NHS Trust -Teaching
    Birmingham
    England
    B9 5SS
  • Queen's Hospital, Burton
    Burton-upon-Trent
    England
    DE14 3QH
  • Broomfield Hospital
    Chelmsford, Essex
    England
    CM1 5ET
  • Northampton General Hospital NHS Trust
    Northampton
    England
  • Thornbury Hospital
    Sheffield
    England
    S10 3BR
  • West Suffolk Hospital
    Suffolk
    England
    IP33 2QZ
  • Worcester Royal Hospital
    Worcester
    England
    WR5 1JG
  • Velindre Cancer Center at Velinde Hospital
    Cardiff
    Wales
    CF4 7XL
  • Hairmyres Hospital
    East Kilbride
    G75 8RG
  • Hull Royal Infirmary
    Hull
    HU3 2KZ
  • Glan Clywd District General Hospital
    Rhyl, Denbighshire
    LL 18 5UJ
  • Singleton Hospital
    Swansea
    SA 2 8QA
  • Morriston Hospital NHS Trust
    West Glamorgen
    SA6 6NL
  • Royal Devon and Exeter Hospital
    Exeter
    England
    EX2 5DW
  • Western General Hospital
    Edinburgh
    Scotland
    EH4 2XU


The study is sponsored by Cancer Research Campaign Clinical Trials Centre




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Read full details for Trial ID: NCT00039546
Last updated 06 August 2013

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