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Enrolling by invitationNCT05868252Updated May 22, 2023

Molecular Analysis of the Sloane Project

An observational study in DCIS, LCIS and Atypical Ductal Hyperplasia, sponsored by King's College London. Enrolling by invitation at 1 site in United Kingdom. Open to female participants. Per ClinicalTrials.gov, last updated 2023-05-22.

Sponsored by King's College London · Observational

From the registry’s dates

  • Primary completion was expected by May 2024, 2 years 4 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
1,500
Sex
Female
01

Study summary

The Sloane Project is a UK wide prospective audit of screen detected non-invasive and atypical breast hyperplasias named after John Sloane an eminent pathologist interested in the field. Non invasive breast neoplasia accounts for 25% of all 'breast cancers' detected through breast screening and includes ductal carcinoma in situ (DCIS) and lobular carcinoma in situ (LCIS). Atypical hyperplasias are high risk but benign lesions found in 10% of benign biopsies performed through the NHS breast screening programme. The importance of these lesions rests on the increased risk of subsequently developing invasive breast cancer, with DCIS at highest risk (20 times greater than the general population) followed by LCIS (10 times greater) and atypical breast hyperplasia (4 times greater).

The Sloane Project data are held by Public Health England (PHE) and provide full and detailed information about the patients' journey from diagnosis to treatment and outcome. The project aims to increase the understanding of how best to manage these early lesions which can lead to breast cancer.

All NHS breast screening units in the UK are invited to submit data for the Sloane Project. Historically an exceptional \~90% of centres in England, Scotland, Wales and Northern Ireland have participated on a voluntary basis.

The objective of this research protocol is the collection of anonymised formalin fixed paraffin embedded (FFPE) tissue blocks from women whose data is held within the Sloane Project database in order to allow detailed analysis of the biological, molecular and genomic changes in these cases of in situ carcinoma and atypical hyperplasia and how these relate to the corresponding annotated clinical, pathological and radiological data already collected by and held in PHE. We seek to identify particular signature(s) that define which patients are likely to develop invasive disease, distinguishing the worrisome from indolent, non-worrisome lesions.

02

Conditions studied

  • DCIS
  • LCIS
  • Atypical Ductal Hyperplasia
  • Atypical Lobular Hyperplasia
03

In context

Carcinoma, Intraductal, Noninfiltrating

205 studies on the registry are indexed under Carcinoma, Intraductal, Noninfiltrating; 46 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 200 across 39 observational studies indexed under Carcinoma, Intraductal, Noninfiltrating.

Browse Carcinoma, Intraductal, Noninfiltrating studies →

Lead sponsor

King's College London is the lead sponsor of 506 studies on the registry; 125 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Those who have undergone breast screening and were part of the Sloane Project audit

Eligibility criteria

Inclusion Criteria:

  • DCIS (Ductal Carcinoma in situ)
  • LCIS (Lobular Carcinoma in situ)
  • Atypical hyperplasias
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
1,500 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Progression of breast disease

    Time frame: From diagnosis to end of 2016

07

Study locations

1 site
  • King's College London
    London, SE1 9RT, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05868252
Lead sponsor
King's College London
Responsible party
Sponsor
First posted
May 22, 2023
Start date
Mar 1, 2020
Primary completion
May 19, 2024 (estimated)
Completion
May 19, 2024 (estimated)
Last update
May 22, 2023

Study contacts

Elinor Sawyer
principal investigator · King's College London

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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