Malmö Breast Tomosynthesis Screening Trial (MBTST)
Primary Purpose
Breast Cancer
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
DBT and FFDM
Sponsored by

About this trial
This is an interventional prevention trial for Breast Cancer focused on measuring breast cancer, screening, sensitivity, tomosynthesis
Eligibility Criteria
Inclusion Criteria:
- women 40-74 years old
- in the regular population based mammographic screening program in Malmö, Sweden.
Exclusion Criteria: pregnancy and women not speaking English or Swedish
-
Sites / Locations
- Malmö Breast Screening Unit, Skåne University Hospital
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
FFDM+DBT
Arm Description
Single-armed study. Women are their own controls with paired images of digital mammography and breast tomosynthesis.
Outcomes
Primary Outcome Measures
Sensitivity and specificity for breast cancer detection for DBT and DM respectively
Sensitivity and specificity for breast cancer detection will be assessed for DBT and DM respectively. The following screening performance measures will also also investigated: the number of detected cancers per 1000 women screened, the number of recalled women/100 screens (recall rate) after consensus, and the positive predictive value (PPV) for screen-recall and the negative predictive value (NPV), in both reading arms. Analyses of the contribution from different reading steps will be investigated. A follow-up period of 24 months after the intervention period will provide information on the actual numbers of breast cancers in the study population through record linkage with the Swedish Cancer Registry.
Secondary Outcome Measures
What kind of cancers are detected and not detected with DBT?
To investigate the biological characteristics of the cancers in the trial by mode of detection (screening detected, interval cancers)
Cost-effectiveness of DBT in screening
to investigate the cost-effectiveness of DBT in screening
Full Information
NCT ID
NCT01091545
First Posted
March 12, 2010
Last Updated
November 11, 2019
Sponsor
Region Skane
Collaborators
Unilabs AB Sweden
1. Study Identification
Unique Protocol Identification Number
NCT01091545
Brief Title
Malmö Breast Tomosynthesis Screening Trial
Acronym
MBTST
Official Title
Malmö Breast Tomosynthesis Screening Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
February 1, 2010 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
September 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
Collaborators
Unilabs AB Sweden
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To compare digital breast tomosynthesis (DBT) with full field digital mammography (FFDM) regarding effectiveness as screening modalities.
Detailed Description
Mammography is the only approved method for breast cancer screening, but not all tumors can be detected with mammography. The main reason is overlapping structures that can either mimic or hide a tumor on a 2-dimensional image like mammography. Digital breast tomosynthesis, (DBT) is a 3-dimensional x-ray technique that has been developed during the last years. A tomographic technique like DBT, which reduces or eliminates the detrimental effect of over- and underlying tissue, can probably help to find more tumors. This study aims to investigate whether more breast cancers can be detected with DBT compared to full field digital mammography (FFDM) in population invited to screening. An interim analysis will be performed during 2013 including the first 7,500 women of the study cohort.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer, screening, sensitivity, tomosynthesis
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15000 (Actual)
8. Arms, Groups, and Interventions
Arm Title
FFDM+DBT
Arm Type
Other
Arm Description
Single-armed study. Women are their own controls with paired images of digital mammography and breast tomosynthesis.
Intervention Type
Radiation
Intervention Name(s)
DBT and FFDM
Intervention Description
Women in the study will once undergo both standard FFDM screening (2-views) and DBT (1 view, MLO). This will result in a doubled radiation dose compared to only 2-view FFDM, which is the standard procedure for women in the screening program.
Primary Outcome Measure Information:
Title
Sensitivity and specificity for breast cancer detection for DBT and DM respectively
Description
Sensitivity and specificity for breast cancer detection will be assessed for DBT and DM respectively. The following screening performance measures will also also investigated: the number of detected cancers per 1000 women screened, the number of recalled women/100 screens (recall rate) after consensus, and the positive predictive value (PPV) for screen-recall and the negative predictive value (NPV), in both reading arms. Analyses of the contribution from different reading steps will be investigated. A follow-up period of 24 months after the intervention period will provide information on the actual numbers of breast cancers in the study population through record linkage with the Swedish Cancer Registry.
Time Frame
24 months after trial screening
Secondary Outcome Measure Information:
Title
What kind of cancers are detected and not detected with DBT?
Description
To investigate the biological characteristics of the cancers in the trial by mode of detection (screening detected, interval cancers)
Time Frame
24 months after trial screening
Title
Cost-effectiveness of DBT in screening
Description
to investigate the cost-effectiveness of DBT in screening
Time Frame
24 months after trial screening
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
women 40-74 years old
in the regular population based mammographic screening program in Malmö, Sweden.
Exclusion Criteria: pregnancy and women not speaking English or Swedish
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sophia Zackrisson, MD PhD
Organizational Affiliation
Region Skane
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ingvar Andersson, MD PhD
Organizational Affiliation
Lund University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Malmö Breast Screening Unit, Skåne University Hospital
City
Malmö
ZIP/Postal Code
SE 20502
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
34870215
Citation
Dahlblom V, Andersson I, Lang K, Tingberg A, Zackrisson S, Dustler M. Artificial Intelligence Detection of Missed Cancers at Digital Mammography That Were Detected at Digital Breast Tomosynthesis. Radiol Artif Intell. 2021 Sep 1;3(6):e200299. doi: 10.1148/ryai.2021200299. eCollection 2021 Nov.
Results Reference
derived
PubMed Identifier
30322817
Citation
Zackrisson S, Lang K, Rosso A, Johnson K, Dustler M, Fornvik D, Fornvik H, Sartor H, Timberg P, Tingberg A, Andersson I. One-view breast tomosynthesis versus two-view mammography in the Malmo Breast Tomosynthesis Screening Trial (MBTST): a prospective, population-based, diagnostic accuracy study. Lancet Oncol. 2018 Nov;19(11):1493-1503. doi: 10.1016/S1470-2045(18)30521-7. Epub 2018 Oct 12. Erratum In: Lancet Oncol. 2019 Jan;20(1):e9.
Results Reference
derived
Learn more about this trial
Malmö Breast Tomosynthesis Screening Trial
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