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Breast CancerPROSPECTSNCT03733106

Prospective Trial of Digital Breast Tomosynthesis (DBT) in Breast Cancer Screening.

A study testing digital breast tomosynthesis and standard two dimension digital mammogram in people with Breast Cancer, run by King's College Hospital NHS Trust at 1 site in United Kingdom.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The accuracy of standard two dimension digital mammography (2DDM) in breast cancer screening is limited because of superimposition of normal breast structures onto a two dimensional image. Mammography signs of breast cancer may be obscured, resulting in delay in the diagnosis of breast cancer. Read more about this study

Who is it for?
Ages 50 to 70 years, women only
Conditions the study is for
Breast Cancer
What is being tested?
digital breast tomosynthesis and standard two dimension digital mammogram
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100,000 participants
Where
1 siteUnited Kingdom
Study dates
17 Dec 2018to Jul 2024
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 50 to 70 years
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • women aged 50-70 years attending for routine breast cancer screening

Who cannot join

  • women aged 47-49 and 71-73 invited to participate in the age extension trial
  • women who are unable to give informed consent

Trial locations and contacts

1 site in 1 country.

Michael J Michell, FRCR contact

0203 299 3875

michael.michell@nhs.net

United Kingdom1 site, 1 recruiting
  • King's College Hospital NHS Foundation Trust

    London

    Recruiting

Other trials in United Kingdom

About this study

Official title: Prospective Randomized Trial of Digital Breast Tomosynthesis (DBT) Plus Standard 2D Digital Mammography (2DDM) or Synthetic 2D Digital Mammography (S2D) Compared to Standard 2DDM in Breast Cancer Screening.

The accuracy of standard two dimension digital mammography (2DDM) in breast cancer screening is limited because of superimposition of normal breast structures onto a two dimensional image. Mammography signs of breast cancer may be obscured, resulting in delay in the diagnosis of breast cancer. Conversely, superimposition of normal tissues may produce features on mammography which are suspicious for cancer and lead to recall for further tests. Digital breast tomosynthesis (DBT) is a new x ray mammography technique which provides three dimensional information to the film reader, overcoming many of the interpretation problems due to tissue superimposition. Studies of DBT + 2DDM in screening have shown increased cancer detection rates and lower false positive recall rates. There may be increased costs related to the technology and reading times.

The aim of this study is to measure the impact and cost effectiveness of DBT + 2DDM in routine screening compared to standard 2DDM.100,000 women wil be recruited using NHS BSP screening sites. At each site, through a clinic randomization process, half of the participants will undergo standard screening with 2DDM (the control group) and half will undergo screening using DBT+2DDM.

Read the detailed description

The accuracy of two view digital x-ray mammography (2DDM), the standard test for breast cancer screening, is limited because of the effect of superimposition of normal breast structures onto a two dimensional image. The mammography signs of breast cancer may be obscured, particularly in women with dense fibro glandular breast tissue, resulting in delay in diagnosis of cancer. National interval cancer data shows that up to 4000 women per annum (2.88 per 1000 screened) are diagnosed with breast cancer in the interval between screens. Conversely, superimposition of normal tissues may produce features on mammography which are suspicious for cancer and lead to unnecessary recall for further diagnostic tests. National screening data for 2012/2013 show that of 2.3 million women screened, 79000 (3.4%) without breast cancer were recalled to specialist diagnostic assessment clinics.

DBT is an x-ray mammography technique which involves acquiring multiple low dose projections over a limited angular range (less than 50 degrees). These projection images are reconstructed into a set of images consisting of parallel planes, typically 1mm apart throughout the breast. Three dimensional information is provided for the reader, overcoming many of the interpretation problems associated with 2DDM. Several studies have demonstrated improvement in the accuracy of DBT in the diagnostic setting. Published data from studies of DBT combined with 2DDM in screening have demonstrated increased rates of invasive cancer detection, cancers detected at a smaller size and decreased false positive recall rates. However, there may be increased costs associated with the technology, image data storage and longer reading time.

As a result of recent technical developments, a two dimensional mammography image can be produced by processing the tomosynthesis image data. Synthetic 2D (S2D) trial data show that the accuracy of DBT + S2D may be the same as that achieved with DBT + 2DDM.

The primary aim of this trial is to assess the impact of the addition of DBT to 2DDM in routine breast cancer screening compared to 2D mammography. 100 000 women will be recruited over twelve months using NHS screening sites with DBT ready mammography equipment. At each site, through a clinic randomisation process, half the trial participants will undergo standard 2DDM (the control group) and half will undergo 2DDM and DBT (the study group). Synthetic 2D images will be produced for all women in the intervention group. A secondary objective of the trial is to compare the accuracy of DBT + 2DDM with DBT + S2D. For each woman in the intervention group, one reader will view DBT + 2DDM, and the other reader will view DBT + S2D. This will enable a non-inferiority test to be applied to DBT + S2D vs DBT + 2DDM.

The investigators plan to use DBT in addition to 2DDM in the intervention group because:

  • Most previous trials demonstrated increased sensitivity and specificity by using DBT in combination with 2D imaging rather than as a replacement.
  • By using both 2D and DBT in the study group, the investigators will be able to review the display of the same cancer in the two techniques.

One concern about using DBT in conjunction with 2D imaging is the increase in radiation dose. The investigators conservatively estimate the mean glandular radiation dose of 4mGy in the control group and 9mGy in the study group. In other words, DBT imaging requires slightly more than double the dose of 2D imaging. A recent study of Yaffe \& Mainprize 2011 has shown that benefits of screening with mammography greatly exceed the detriment due to the radiation. Using similar calculations the investigators estimate that the ratio of lives saved and lost due to radiation in the 2DDM screening arm will be in the range 150-300 to 1. The higher dose in the study group is expected to lead to greater benefit and greater detriment. In order for the extra benefit to exceed the extra detriment of using DBT in the study group there will need to be a very small (0.45% to 0.9%) increase in lives saved. In practice the investigators expect a larger benefit that this.

  • Health need: the effectiveness of 2DDM in detection of invasive breast cancer has improved over the last twenty years as demonstrated by a decrease in interval cancer rates (cancers occurring between routine three yearly screens). This improvement is a result of the introduction of two view mammography, digital mammography and improvements in film reading performance. However, the most recent published interval cancer rates of 2.85 per 1000 women screened demonstrates the limited sensitivity of 2DDM in cancer detection. Published data from studies of DBT and 2DDM in screening in Europe and North America demonstrate an increased invasive cancer detection rate of 40-48% compared to 2DDM alone. Data from this study will demonstrate whether such an improvement in sensitivity is achievable in the NHSBSP, whether cancers can be detected at a smaller size, and prognostic features of screen detected and interval cancers will be used to model whether there would be a greater reduction in breast cancer mortality from screening with 2DDM plus DBT compared to 2D alone. Data will also demonstrate the effect on false positive recalls in the NHSBSP. Published results show that this may be decreased by 15-20% with the use of DBT.
  • Economic analysis: The study will demonstrate whether replacing standard 2DDM with DBT (and S2D) represents an efficient use of NHS resources, either because DBT reduces overall cost or because the additional health benefits of greater sensitivity and specificity justify the additional cost.
  • Sustained interest: DBT may have a major impact on the effectiveness and the cost of screening. Data from this study will help decide the optimum strategy for using DBT in routine screening in the NHS.
  • Development of research area: results from this study will help identify which groups of women will benefit from screening with DBT.
  • Scientific knowledge: this study will advance our understanding of the effect of DBT on the characteristics of screen detected cancers, whether more biologically significant cancers are found when smaller and at an earlier stage, and whether more low grade cancers are diagnosed, increasing the problem of over diagnosis.
Conditions
Breast Cancer
Being tested
digital breast tomosynthesis, standard two dimension digital mammogram
Keywords
screening, tomosynthesis
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • digital breast tomosynthesisDiagnostic test

    pseudo three dimension mammography

  • standard two dimension digital mammogramDiagnostic test

    standard two dimension mammogram

Study groups in NCT03733106
Study groupRoleWhat they receive
digital breast tomosynthesisExperimentalTomosynthesis and two dimension digital mammography
Receives: Diagnostic Test: digital breast tomosynthesis
controlActive comparatorstandard two dimension digital mammography
Receives: Diagnostic Test: standard two dimension digital mammogram

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To compare the cost effectiveness of breast cancer screening with digital breast tomosynthesis and 2DDM vs standard screening with 2DDM

    To compare the effectiveness of breast cancer screening with DBT and 2D mammography with standard 2D mammography screening by measuring the internal cancer rate in women undergoing DBT and 2D mammography VS the interval cancer rate in women undergoing standard 2D mammography.

    (Estimated interval cancer rates - intervention group 1.85/1000 screened; control group 2.85/1000 screened)

    Measured: outcome measures to be reported from 2-7 years following beginning of recruitment into the trial

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Nov 2018
  2. Study start17 Dec 2018
  3. Primary completionJul 2024 (estimated)
  4. Study completionJul 2024 (estimated)

Resources

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
Screening
Allocation
Randomised
Intervention model
Parallel groups
Model description
Prospective randomized controlled study
Masking
Single blind
Who is masked
Participant
Enrolment
100,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03733106
Sponsor's protocol ID
199080
Acronym
PROSPECTS
Status last verified
Nov 2019
First submitted
10 Oct 2017
Last updated
6 Nov 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no plan to make individual participant data available to individuals outside the research team

Publications

  • J W Partridge G, Darker I, J James J, Satchithananda K, Sharma N, Valencia A, Teh W, Khan H, Muscat E, J Michell M, Chen Y. How long does it take to read a mammogram? Investigating the reading time of digital breast tomosynthesis and digital mammography. Eur J Radiol. 2024 Aug;177:111535. doi: 10.1016/j.ejrad.2024.111535. Epub 2024 May 29.

    PubMed 38852330
  • Partridge GJW, Taib AG, Phillips P, James JJ, Satchithananda K, Sharma N, Morel J, McAvinchey R, Valencia A, Teh W, Khan H, Muscat E, Michell MJ, Chen Y. Take a break: should breaks be enforced during digital breast tomosynthesis reading sessions? Eur Radiol. 2024 Feb;34(2):1388-1398. doi: 10.1007/s00330-023-10086-4. Epub 2023 Aug 17.

    PubMed 37589906

Questions about this trial

What is this clinical trial studying?

A study testing digital breast tomosynthesis and standard two dimension digital mammogram in people with Breast Cancer, run by King's College Hospital NHS Trust at 1 site in United Kingdom.

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 1 inclusion and 2 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 6 Nov 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. 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 Michael J Michell, FRCR (0203 299 3875, michael.michell@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To compare the cost effectiveness of breast cancer screening with digital breast tomosynthesis and 2DDM vs standard screening with 2DDM (time frame: outcome measures to be reported from 2-7 years following beginning of recruitment into the trial). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03733106, which also lists 2 linked publications.

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 6 Nov 2019.

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