Early Breast CancerTARGIT-BNCT01792726
A Comparison of Intra-operative Radiotherapy Boost With External Beam Radiotherapy Boost in Early Breast Cancer.
A study testing Boost to the tumour bed in people with Early Breast Cancer, run by University College, London at 34 sites in 12 countries.
Trial summary
TARGIT-Boost is an international randomised clinical trial designed to test the hypothesis that the tumour bed boost delivered as a single dose of targeted intraoperative radiotherapy (TARGIT-B) is superior to the conventional course of external beam radiotherapy boost (EBRT-Boost), especially in women with high risk… Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- Early Breast Cancer
- What is being tested?
- Boost to the tumour bed
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,796 participants
- Where
- 34 sitesin 12 countries
- Study dates
- Jun 2013to Apr 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Women only
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- At least one of these criteria must be satisfied:
- Less than 46 years of age
- More than 45 years of age, but with one of the following poor prognostic factors:
- lymphovascular invasion
- gross nodal involvement (not micrometastasis)
- more than one tumour in the breast but still suitable for breast conserving surgery through a single specimen
Show all 14Show fewer
- More than 45 years of age, but with at least two of the following poor prognostic factors
- ER and/or PgR negative
- Grade 3 histology
- Positive margins at first excision
- Those patients with large tumours which have responded to neo-adjuvant chemo- or hormone therapy in an attempt to shrink the tumour and are suitable for breast conserving surgery as a result.
- Lobular carcinoma or Extensive Intraductal Component (EIC)
- A list (one to many) of high risk factors are present (as predefined in the policy document) that give a high risk of local recurrence.
- Patients with either HER2 positive or HER2 negative can be included.
Who cannot join
- Bilateral breast cancer at the time of diagnosis.
- 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 (e.g., non-melanoma skin cancer, CIN, etc).
- No more than 30 days can have elapsed between last breast cancer surgery (not axillary) and randomisation for patients in the post-pathology stratification unless part of a specific clinical trial that addresses the question of timing or tumour bed can be reliably identified, e.g., by ultrasound.
Trial locations and contacts
34 sites in 12 countries.
34 sites in 12 countries
United States8 sites, 7 recruiting
- Recruiting
Cleveland Clinic
Cleveland, Ohio
Courtney Yanda, yandac@ccf.org
Stephanie Valente
- Recruiting
Beaumont Health - Royal Oak
Detroit, Michigan
Blerina Pople, Blerina.pople@beaumont.org
Nayana Dekhne, MD
- Recruiting
Ashikari Breast Center
Dobbs Ferry, New York, 10522
Pond Kelemen, MD
- Recruiting
Aurora Breast Center
Green Bay, Wisconsin
Corinne Zipperer, RN, corinne.zipperer@aurora.org
William Owens
- Recruiting
Helen Rey Breast Cancer Research Foundation
Los Angeles, California
Alexandra Banks, alexandra@drholmesmd.com
Dennis R Holmes, MD
- Recruiting
West Virginia University
Morgantown, West Virginia
Cortney Montgomery, comontgomery@hsc.wvu.edu
Geraldine Jacobson
- Recruiting
Lakeland Regional Health System
Saint Joseph, Michigan
Pamela Stephenson, pstephenson@lakelandhealth.org
Benjamin T Gielda
- Active, not recruiting
Memorial Health University Medical Center
Savannah, Georgia
United Kingdom8 sites, 7 recruiting
- Recruiting
Princess Alexandra Hospital NHS Trust
Harlow
Julian Singer, MD
- Recruiting
Whittington Hospital
London, N19 5NF
Jayant S Vaidya, MBBS FRCS, jayant.vaidya@ucl.ac.uk
Jayant S Vaidya, MBBS FRCS
- Recruiting
Royal Free London NHS Trust
London, NW3 2QG
Mo Keshtgar, MB BS, m.keshtgar@ucl.ac.uk
Mo Keshtgar, MB BS
- Recruiting
Guy's Hospital
London
Sweta Sethi
Michael Douek
- Recruiting
Hospital of St John and St Elizabeth
London
Mo Keshtgar, MB BS, m.keshtgar@ucl.ac.uk
Mo Keshtgar, MB BS
- Active, not recruiting
Princess Grace Hospital
London
- Recruiting
The Great Western Hospital
Swindon, SN3 6BB
Nathan Coombs, MB BS
- Recruiting
Hampshire Hospitals NHS Foundation Trust
Winchester
Elizabeth Happle, Elizabeth.happle@hhft.nhs.uk
Sanjay Raj
France7 sites, 7 recruiting
- Recruiting
Institut Bergonié
Bordeaux
Christel Breton-Callu, MD
- Recruiting
Centre François Baclesse
Caen
Boly Ann, boly.ann@mail.baclesse.fr
Serge Danhier, MD
- Recruiting
Centre Georges François Leclerc
Dijon
Etienne Martin, MD
- Recruiting
Centre Léon Bérard
Lyon
Christelle Faure, MD
- Recruiting
Hôpital Nord
Marseille
Didier Cowen, MD
Didier Cowen, MD
- Recruiting
Institut de Cancerologie de l'Ouest site René Gauducheau
Nantes, 44805
Magali Le Blanc, MD
- Recruiting
Institut Universitaire du Cancer de Toulouse - Oncopole
Toulouse
Francoise Izar, MD
Francoise Izar, MD
Italy2 sites, 2 recruiting
- Recruiting
Centro Di Riferimento Oncologico Di Aviano
Aviano
Samuele Massarut, MD
Samuele Massarut, MD
- Recruiting
Istituto Oncologico Veneto
Padova
Fabiana Gregucci
Fernando Bozza
Spain2 sites, 2 recruiting
- Recruiting
Institut Català d'Oncologia
Barcelona
Montse Ventura, montseventura@iconcologia.net
Evelyn Martínez Pérez
- Recruiting
Hospital Universitario Dr Negrín
Las Palmas de Gran Canaria
Pedro C Lara, MD
China1 site, 1 recruiting
- Recruiting
Beijing Cancer Hospital
Beijing
Xinguang Wang
Tao Ouyang
Malaysia1 site, 1 recruiting
- Recruiting
University Malaya Medical Centre
Kuala Lumpur
Zarinah Abdul Rahman, zarinahar@ummc.edu.my
Nur Aishah Mohd Taib
Saudi Arabia1 site, 1 recruiting
- Recruiting
University of Dammam
Dammam
Maha Abdel Hadi
South Africa1 site, 1 recruiting
- Recruiting
Netcare Milpark Hospital
Johannesburg
Kyara Bergstrom
Carol Benn
South Korea1 site, 1 recruiting
- Recruiting
Gangnam Severance Hospital
Seoul
Sung Gwe Ahn
Joon Jeong
Switzerland1 site, 1 recruiting
- Recruiting
Brust-Zentrum Onkologie
Zurich
Bärbel Papassotiropoulos
Thailand1 site, 1 recruiting
- Recruiting
Queen Sirikit Cantre for Breast Cancer
Bangkok
Sikrit Denariyakoon
Adhisabandh Chulakadabba
About this study
Official title: An International Randomised Controlled Trial to Compare Targeted Intra-operative Radiotherapy Boost With Conventional External Beam Radiotherapy Boost After Lumpectomy for Breast Cancer in Women With a High Risk of Local Recurrence.
TARGIT-Boost is an international randomised clinical trial designed to test the hypothesis that the tumour bed boost delivered as a single dose of targeted intraoperative radiotherapy (TARGIT-B) is superior to the conventional course of external beam radiotherapy boost (EBRT-Boost), especially in women with high risk of local recurrence. It is a pragmatic trial in which each participating centre can use the local predefined inclusion/exclusion criteria for entry into the trial. Only centres with access to the Intrabeam® (Carl Zeiss) are eligible to enter patients into the trial.
Eligible patients are those with a higher risk of local recurrence after breast conserving surgery.
Read more
After giving consent patients are randomised to either TARGIT Boost or EBRT Boost. All patients will receive whole breast EBRT. They may receive any other adjuvant treatments as deemed necessary. The protocol recommends that patients be followed at six monthly intervals for three years and then annually.
The primary endpoint is ipsilateral breast recurrence rate. Secondary endpoints are relapse-free survival, site of recurrence, overall survival (breast-cancer specific and non-breast cancer deaths) patient satisfaction and quality of life.
Read the detailed description
DESIGN: A pragmatic multi-centre randomised clinical trial to test whether TARGeted Intraoperative radioTherapy as a tumour bed Boost (TARGIT-B) is superior in terms of local relapse within the treated breast compared with standard post-operative external beam radiotherapy boost in women undergoing breast conserving therapy who have a higher risk of local recurrence. Patients can be entered before the primary surgery or in a smaller proportion of cases, post-pathology. SETTING: Specialist breast units in UK, USA, Canada, Australia and Europe; 31 centres currently recruiting in the TARGIT-A trial and several are ready to join. TARGET POPULATION: Breast cancer patients suitable for breast conserving surgery, but with a high risk of local recurrence. Details of inclusion and exclusion are given in part 2. Briefly the patients should be either younger than 45 or if older, need to have certain pathological features that confer a high risk of local recurrence of breast cancer. HEALTH TECHNOLOGIES BEING ASSESSED. The TARGIT Technique: The Intrabeam® (Carl Zeiss, FDA approved and CE marked) is a miniature electron beam-driven source which provides a point source of low energy X-rays (50kV maximum) at the tip of a 3.2mm diameter tube. The radiation source is inserted into the tumour bed immediately after excision of the tumour and switched on for 20-35 minutes to provide intra-operative radiotherapy accurately targeted to the tissues that are at highest risk of local recurrence. The physics, dosimetry and early clinical applications of this soft x-ray device have been well studied. For use in the breast, the technique was first developed and piloted at University College London. The radiation source is surrounded by a spherical applicator, specially designed (and available in various sizes) to produce a uniform field of radiation at its surface, enabling delivery of an accurately calculated dose to a prescribed depth. It is inserted in the tumour bed and apposed to it with surgical sutures and/or other means. As the x-rays rapidly attenuate the dose to more distant tissues is reduced; this also allows it to be used in standard operating theatres. 20 Gy is delivered to the tumour bed surface in 20-35 minutes, after which the radiation is switched off, the applicator removed, and the wound closed in the normal way. This simple technique has potentially several advantages over convential external beam radiotherapy, interstitial implantation of radioactive wires or conformal external beam radiotherapy. The first pilot of twenty-five cases was at performed at UCL using TARGIT technique as a replacement for the boost dose of radiotherapy; full dose external beam treatment was subsequently given. The phase II study of 300 patients was published and recently updated with long term data along with favourable toxicity and cosmetic outcome results of individual cohorts. A mathematical model of TARGIT developed recently (funded by Cancer Research UK) suggests that it could be superior to conventional radiotherapy. Translational research has found that TARGIT impairs the surgical-trauma-stimulated proliferation and invasiveness of breast cancer cells. This effect of radiotherapy may act synergistically with its tumouricidal effect yielding a superior result. MEASUREMENT OF COST AND OUTCOME: Patient assessments will be clinical examination (6 monthly x 3 years then yearly x 10 years) and mammography (yearly). with ulstrasound (if needed) . Primary outcome: histologically/cytologically proven local recurrence. Secondary: site of relapse in the breast, overall survival, local toxicity (RTOG and LENT SOMA criteria), cosmesis, quality of life, patient satisfaction and health economics. The cost and cost-effectiveness of TARGIT versus EBRT, both as boost, will be calculated from a NHS and personal social services (PSS) perspective. Costs directly incurred by patients will also be assesed, since EBRT as a boost is likely to impose additional time and travel expense to patients and families.
- Conditions
- Early Breast Cancer
- Being tested
- Boost to the tumour bed
- Keywords
- breast cancer, radiotherapy, TARGIT, Intrabeam
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Boost to the tumour bedRadiation
Also called Radiotherapy boost
Boost to the tumour bed, with whole breast EBRT delivered according to local policy.
| Study group | Role | What they receive |
|---|---|---|
| TARGIT | Experimental | The experimental policy is to give targeted intra-operative radiotherapy (TARGIT-Boost) in a single dose to substitute for the usual boost dose, in addition to whole breast external beam radiotherapy delivered according to local treatment guidelines. Receives: Radiation: Boost to the tumour bed |
| External beam radiotherapy boost | Active comparator | The conventional policy is to receive radiation boost to the tumour bed delivered by external beam radiotherapy (EBRT) in addition to whole breast external beam radiotherapy delivered according to local treatment guidelines. Receives: Radiation: Boost to the tumour bed |
What is being measured
The primary outcome is the main question the study is designed to answer.
Local tumour control (defined as no recurrent tumour in the ipsilateral breast).
To evaluate whether a tumour bed boost in the form of a single fraction of radiotherapy given intra-operatively and targeted to the tissues at the highest risk of local recurrence is superior (in terms of local tumour control) to standard post-operative external beam radiotherapy boost, after breast conserving surgery in women undergoing breast conserving therapy who have a higher risk of local recurrence.
Measured: Five year median follow-up
Secondary outcomes (5)
Site of relapse within the treated breast
Site of relapse within the breast will be recorded in order to assess whether the recurrence is at the site of the initial tumour or at a new site and whether it has occurred within the treated field (TARGIT or EBRT boost).
Measured: 5 years median follow-up
Relapse-free survival
Relapse-free survival will be recorded as the time interval between randomisation and the date of confirmation of recurrence. The actual date to be used is the clinic day on which the investigations that led to a confirmed diagnosis of the recurrence were requested. Relapse-free survival will include any recurrence of breast cancer or death without a prior report of relapse.
Measured: Five year median follow-up
Overall survival
Overall survival will be the time interval between randomisation and death.
Measured: Five year median follow-up.
Adverse events related to the primary treatment of the breast cancer.
Local toxicity and morbidity will be recorded as adverse events related to the primary treatment of the breast cancer. Quality of life will be assessed though validated patient-completed questionnaires.
Measured: Five year median follow-up.
Quality of life assessed by patient completed validated questionnaires.
The primary patient reported outcome endpoint for quality of life will be the FACT-B+4 trial outcome index (TOI) score. The TOI score (0-180) is a sum of the scores of the 27 items included in the physical well-being, functional well-being and breast cancer subscales of the FACT-B+4. A change of at least 5 points in TOI is considered to be clinically relevant or a minimally important difference (Eton et al. 2004). Secondary endpoints will be: 1) the five item arm functioning subscale score (0-20) 2) The 40 item FACT B+4 score (0-160), which reflects global quality of life including social and emotional well-being.
Measured: Five year median follow-up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Feb 2013 (estimated)
- Study startJun 2013
- Primary completionJan 2022 (estimated)
- Study completionApr 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Early Breast CancerStudies of the same condition, open and under way.
- More trials run by University College, LondonThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 1,796 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University College, London
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute for Health Research, United Kingdom
- Responsible party
- Sponsor
- Investigators
- Jayant S Vaidya, MBBS FRCS, Principal investigator, University College, London
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01792726
- Sponsor's protocol ID
- TARGIT Boost
- Other IDs
- NHS NIHR HTA
- Acronym
- TARGIT-B
- Status last verified
- Jul 2019
- First submitted
- 12 Feb 2013
- Last updated
- 12 Jul 2019
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 12 Jul 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An International Randomised Controlled Trial to Compare Targeted Intra-operative Radiotherapy Boost With Conventional External Beam Radiotherapy Boost After Lumpectomy for Breast Cancer in Women With a High Risk of Local Recurrence.
- ClinicalTrials.gov ID
- NCT01792726
- Acronym / sponsor ID
- TARGIT-B / TARGIT Boost
- Conditions
- Early Breast Cancer
- Keywords
- breast cancer, radiotherapy, TARGIT, Intrabeam
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 1,796 participants (estimated)
- Lead sponsor
- University College, LondonUniversity, hospital or other
- Collaborators
- National Institute for Health Research, United Kingdom
- Study start
- Jun 2013
- Primary completion
- Jan 2022 (estimated)
- Study completion
- Apr 2022 (estimated)
- First posted
- 15 Feb 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
TARGIT-Boost is an international randomised clinical trial designed to test the hypothesis that the tumour bed boost delivered as a single dose of targeted intraoperative radiotherapy (TARGIT-B) is superior to the conventional course of external beam radiotherapy boost (EBRT-Boost), especially in women with high risk of local recurrence. It is a pragmatic trial in which each participating centre can use the local predefined inclusion/exclusion criteria for entry into the trial. Only centres with access to the Intrabeam® (Carl Zeiss) are eligible to enter patients into the trial.
Eligible patients are those with a higher risk of local recurrence after breast conserving surgery.
After giving consent patients are randomised to either TARGIT Boost or EBRT Boost. All patients will receive whole breast EBRT. They may receive any other adjuvant treatments as deemed necessary. The protocol recommends that patients be followed at six monthly intervals for three years and then annually.
The primary endpoint is ipsilateral breast recurrence rate. Secondary endpoints are relapse-free survival, site of recurrence, overall survival (breast-cancer specific and non-breast cancer deaths) patient satisfaction and quality of life.
Detailed description
DESIGN: A pragmatic multi-centre randomised clinical trial to test whether TARGeted Intraoperative radioTherapy as a tumour bed Boost (TARGIT-B) is superior in terms of local relapse within the treated breast compared with standard post-operative external beam radiotherapy boost in women undergoing breast conserving therapy who have a higher risk of local recurrence. Patients can be entered before the primary surgery or in a smaller proportion of cases, post-pathology. SETTING: Specialist breast units in UK, USA, Canada, Australia and Europe; 31 centres currently recruiting in the TARGIT-A trial and several are ready to join. TARGET POPULATION: Breast cancer patients suitable for breast conserving surgery, but with a high risk of local recurrence. Details of inclusion and exclusion are given in part 2. Briefly the patients should be either younger than 45 or if older, need to have certain pathological features that confer a high risk of local recurrence of breast cancer. HEALTH TECHNOLOGIES BEING ASSESSED. The TARGIT Technique: The Intrabeam® (Carl Zeiss, FDA approved and CE marked) is a miniature electron beam-driven source which provides a point source of low energy X-rays (50kV maximum) at the tip of a 3.2mm diameter tube. The radiation source is inserted into the tumour bed immediately after excision of the tumour and switched on for 20-35 minutes to provide intra-operative radiotherapy accurately targeted to the tissues that are at highest risk of local recurrence. The physics, dosimetry and early clinical applications of this soft x-ray device have been well studied. For use in the breast, the technique was first developed and piloted at University College London. The radiation source is surrounded by a spherical applicator, specially designed (and available in various sizes) to produce a uniform field of radiation at its surface, enabling delivery of an accurately calculated dose to a prescribed depth. It is inserted in the tumour bed and apposed to it with surgical sutures and/or other means. As the x-rays rapidly attenuate the dose to more distant tissues is reduced; this also allows it to be used in standard operating theatres. 20 Gy is delivered to the tumour bed surface in 20-35 minutes, after which the radiation is switched off, the applicator removed, and the wound closed in the normal way. This simple technique has potentially several advantages over convential external beam radiotherapy, interstitial implantation of radioactive wires or conformal external beam radiotherapy. The first pilot of twenty-five cases was at performed at UCL using TARGIT technique as a replacement for the boost dose of radiotherapy; full dose external beam treatment was subsequently given. The phase II study of 300 patients was published and recently updated with long term data along with favourable toxicity and cosmetic outcome results of individual cohorts. A mathematical model of TARGIT developed recently (funded by Cancer Research UK) suggests that it could be superior to conventional radiotherapy. Translational research has found that TARGIT impairs the surgical-trauma-stimulated proliferation and invasiveness of breast cancer cells. This effect of radiotherapy may act synergistically with its tumouricidal effect yielding a superior result. MEASUREMENT OF COST AND OUTCOME: Patient assessments will be clinical examination (6 monthly x 3 years then yearly x 10 years) and mammography (yearly). with ulstrasound (if needed) . Primary outcome: histologically/cytologically proven local recurrence. Secondary: site of relapse in the breast, overall survival, local toxicity (RTOG and LENT SOMA criteria), cosmesis, quality of life, patient satisfaction and health economics. The cost and cost-effectiveness of TARGIT versus EBRT, both as boost, will be calculated from a NHS and personal social services (PSS) perspective. Costs directly incurred by patients will also be assesed, since EBRT as a boost is likely to impose additional time and travel expense to patients and families.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| TARGIT | Experimental | Radiation: Boost to the tumour bedThe experimental policy is to give targeted intra-operative radiotherapy (TARGIT-Boost) in a single dose to substitute for the usual boost dose, in addition to whole breast external beam radiotherapy delivered according to local treatment guidelines. |
| External beam radiotherapy boost | Active comparator | Radiation: Boost to the tumour bedThe conventional policy is to receive radiation boost to the tumour bed delivered by external beam radiotherapy (EBRT) in addition to whole breast external beam radiotherapy delivered according to local treatment guidelines. |
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (14 listed)
- Less than 46 years of age
- More than 45 years of age, but with one of the following poor prognostic factors:
- More than 45 years of age, but with at least two of the following poor prognostic factors
- Those patients with large tumours which have responded to neo-adjuvant chemo- or hormone therapy in an attempt to shrink the tumour and are suitable for breast conserving surgery as a result.
- Lobular carcinoma or Extensive Intraductal Component (EIC)
Key exclusion criteria (4 listed)
- Bilateral breast cancer at the time of diagnosis.
- 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 (e.g., non-melanoma skin cancer, CIN, etc).
- No more than 30 days can have elapsed between last breast cancer surgery (not axillary) and randomisation for patients in the post-pathology stratification unless part of a specific clinical trial that addresses the question of timing or tumour bed can be reliably identified, e.g., by ultrasound.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Boost to the tumour bedAlso: Radiotherapy boostBoost to the tumour bed, with whole breast EBRT delivered according to local policy. | Radiation | External beam radiotherapy boost, TARGIT |
Primary outcome
Local tumour control (defined as no recurrent tumour in the ipsilateral breast).
Time frame: Five year median follow-up
To evaluate whether a tumour bed boost in the form of a single fraction of radiotherapy given intra-operatively and targeted to the tissues at the highest risk of local recurrence is superior (in terms of local tumour control) to standard post-operative external beam radiotherapy boost, after breast conserving surgery in women undergoing breast conserving therapy who have a higher risk of local recurrence.
5 secondary outcomes
Site of relapse within the treated breast
Time frame: 5 years median follow-up
Relapse-free survival
Time frame: Five year median follow-up
Overall survival
Time frame: Five year median follow-up.
Adverse events related to the primary treatment of the breast cancer.
Time frame: Five year median follow-up.
Quality of life assessed by patient completed validated questionnaires.
Time frame: Five year median follow-up
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Jul 2019.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jayant S Vaidya, MBBS FRCS principal investigator
University College, London
34 sites in 12 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Boost to the tumour bed in people with Early Breast Cancer, run by University College, London at 34 sites in 12 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 12 Jul 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 34 sites in United States, United Kingdom, France, Italy, Spain and 7 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Norman R Williams, PhD (+44 (0)20 7679 9280, SITU.TARGITB@ucl.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Local tumour control (defined as no recurrent tumour in the ipsilateral breast). (time frame: Five year median follow-up). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jul 2019.