Comparison of Intra-operative Radiotherapy With Post-operative Radiotherapy for Women With Early Breast Cancer (TARGIT)

This study has been completed.
Sponsor:
Collaborator:
National Institute for Health Research, United Kingdom
Information provided by (Responsible Party):
Norman Williams, University College London Hospitals
ClinicalTrials.gov Identifier:
NCT00983684
First received: September 23, 2009
Last updated: October 8, 2012
Last verified: October 2012

September 23, 2009
October 8, 2012
March 2000
June 2012   (final data collection date for primary outcome measure)
Local relapse within the treated breast. [ Time Frame: 3, 6, 12, 18, 24, 30, 36, 42, 48, 54, 60, 72, 84, 96, 108, 120 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00983684 on ClinicalTrials.gov Archive Site
  • Site of relapse within the breast [ Time Frame: 3, 6, 12, 18, 24, 30, 36, 42, 48, 54, 60, 72, 84, 96, 108, 120 months ] [ Designated as safety issue: No ]
  • Relapse-free survival and overall survival [ Time Frame: 3, 6, 12, 18, 24, 30, 36, 42, 48, 54, 60, 72, 84, 96, 108, 120 months ] [ Designated as safety issue: No ]
  • Local toxicity/morbidity [ Time Frame: 3, 6, 12, 18, 24, 30, 36, 42, 48, 54, 60, 72, 84, 96, 108, 120 months ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Comparison of Intra-operative Radiotherapy With Post-operative Radiotherapy for Women With Early Breast Cancer
TARGIT: A Randomised Controlled Trial to Compare Targeted Intra-operative Radiotherapy With Conventional Post-operative Radiotherapy After Conservative Breast Surgery for Women With Early Stage Breast Cancer

The purpose of this study is to evaluate whether a single fraction of radiotherapy given intra-operatively and targeted to the tissues at the highest risk of local recurrence is equivalent to standard post-operative external beam radiotherapy after breast conserving surgery in women with early stage breast cancer in terms of local relapse within the treated breast.

TARGIT is an international randomised clinical trial designed to test the hypothesis that the strategy of delivering a single dose of targeted intraoperative radiotherapy (IORT) in patients eligible for breast conserving therapy (with the addition of whole breast radiotherapy in those patients at high risk of recurrence elsewhere in the breast [e.g. lobular carcinomas and extensive intraductal component]) is equivalent to a conventional course of post-operative external beam radiotherapy (EBRT). The primary endpoints are local and loco-regional recurrence rates. It is a pragmatic trial in which each participating centre has the option to define more restrictive entry criteria than in the core protocol. Only centres with access to the Intrabeam® (Carl Zeiss) enter patients into the trial. Eligible patients are those with tumours of good prognosis suitable for breast conserving surgery. After giving consent patients are randomised to either IORT or to EBRT. They may receive any other adjuvant treatments as deemed necessary, except for neoadjuvant therapy. The protocol requires that patients be followed at six monthly intervals for five years and then annually.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Invasive Breast Cancer
  • Breast Cancer
  • Device: Intrabeam
    A dose of 20 Gy at the surface of the applicator or 6 Gy at 1cm (in water) is prescribed by the radiation oncologist and delivered to the breast tissue. This takes approximately 30 minutes, depending on the size of the applicator.
    Other Name: IORT, targeted intra-operative radiotherapy, TARGIT
  • Radiation: Post-operative radiotherapy
    All patients randomised to receive conventional radiotherapy within this trial should be treated in accordance with a pre-specified policy. Dosage should only be applied to the breast; axillary, supra-clavicular and internal mammary nodes should not generally be irradiated by discrete fields.
    Other Name: EBRT
  • Experimental: Intra-operative radiotherapy
    A single fraction of radiotherapy given intra-operatively and targeted to the tissues at the highest risk of local recurrence.
    Intervention: Device: Intrabeam
  • Active Comparator: Post-operative radiotherapy
    Standard post-operative radiotherapy.
    Intervention: Radiation: Post-operative radiotherapy

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
3451
June 2012
June 2012   (final data collection date for primary outcome measure)

Inclusion criteria

  • Age 45 years or older
  • Operable invasive breast cancer (T1 and small T2, N0-1, M0) confirmed by cytological or histological examination
  • Suitable for breast conserving surgery
  • Previously diagnosed and treated contralateral breast cancer may be entered but will be randomised to a separate stratum.
  • Available for regular follow-up for at least ten years.

Note: Individual centres may wish to restrict entry to a more exactly defined subset of patients, in which case, only patients with these characteristics may be entered by that particular centre. For example, centres may decide at outset to recruit only women over 50 or even over 65 years of age. Such policies must be pre-defined in writing and approved by the International Steering Committee.

Exclusion criteria

  • More than one obvious cancer in the same breast as diagnosed by clinical examination, mammography or ultrasonography.
  • Bilateral breast cancer at the time of diagnosis.
  • Ipsilateral breast had a previous cancer and/or irradiation.
  • Patients known to have BRCA2 gene mutations, but testing for gene mutations is not required
  • Lobular cancer or Extensive intraductal Component (EIC =>25% of the tumour is intraductal) on core biopsy or initial pathology (if performed)
  • Patients undergoing primary medical treatment (hormones or chemotherapy) as initial treatment with neoadjuvant intent of reducing tumour size should be excluded; those given short duration (up to 4 weeks) systemic therapy can be included.
  • Patients presenting with gross nodal disease, considered to be clinically malignant or proven cytologically or by scanning. In general, 4 or more positive nodes or extranodal spread are not suitable for Targit alone and should receive EBRT as well. However, individual centres may decide that anything more than micrometastasis should receive EBRT.
  • Patients with any severe concomitant disease that may limit their life expectancy.
  • Previous history of malignant disease does not preclude entry if the expectation of relapse-free survival at 10 years is 90% or greater.
  • Any factor included as exclusion criterion in the local centre's Treatment Policy. This is particularly relevant to patients entered into the post pathology stratum.
  • No more than 30 days can have elapsed between last breast cancer surgery (not axillary) and entry into the trial for patients in the post-pathology stratification.
Female
45 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United Kingdom
 
NCT00983684
ISRCTN 34086741, ISRCTN 34086741, MREC No. 99/0307, UKCRN ID 7265
Yes
Norman Williams, University College London Hospitals
Norman Williams
National Institute for Health Research, United Kingdom
Principal Investigator: Jeffrey S Tobias, MD FRCP FRCR University College London Hospitals
University College London Hospitals
October 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP