London Investigation Into diElectric Scanning of Lesions

NCT ID: NCT03302819

Last Updated: 2017-10-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

994 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-01

Study Completion Date

2018-12-01

Brief Summary

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The MARIA breast imaging system is a novel CE-marked radio-frequency (RF) medical imaging device. The system employs an electromagnetic imaging technique that exploits the dielectric contrast between normal and cancerous tissues. The performance and imaging characteristics of MARIA are not yet well demonstrated. The investigators aim to evaluate some aspects of this potentially important new technology.

Detailed Description

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The early diagnosis of breast cancer is of paramount importance, with a 5-year survival rate of 97% if the cancer is caught "locally", deteriorating to 79% if it has progressed to the "axillary" lymph nodes, and 23% if it has spread to the rest of the body, known as "metastasised."

Diagnosis is currently achieved through clinical examination, imaging with mammography (MMG) and/or ultrasound (US) and needle biopsy. Mammography is dependent upon adequate breast compression to allow greater contrast differentiation between tissue structures, this is not only uncomfortable, but in younger women with 'dense' breast tissue the contrast difference between normal tissue and tumour is minimal despite compression. Furthermore mammography uses ionising radiation, which means that a risk/benefit calculation is weighted against repeated or frequent use. Frequently it is necessary to use additional imaging such as ultrasound or MRI for diagnostic support.

Breast tumours have an additional property that can distinguish them from normal and this is defined by the dielectric value. This has two components - the dielectric constant, which affects the velocity of propagation of radio waves and therefore their wavelength, and the conductivity, which affects the rate of attenuation. Typically a tumour has a dielectric constant of 45-50 and a conductivity of 2S/m, whereas breast fat is 5-15 and 0.2-1S/m respectively but with considerable range. Normal glandular tissue is intermediate. These differences in dielectric constant enable a consideration of the value of this data in breast cancer diagnosis.

Several attempts to exploit this property for imaging have been made. The outcomes have been similar in that the presence of a tumour is detectable, however limitations in depth for detection and mode of the technology were identified.

Due to updated technology in the MARIA device, previous limitations from similar studies are not reported to be a problem.

This study aims to determine the proportion of patients with breast cancer who are correctly diagnosed by MARIA, and to stratify this by breast density and histological type. In addition a pilot study will be performed to investigate the imaging characteristics and performance of MARIA in the assessment of benign and malignant lesions in patients attending the symptomatic breast clinic.

The MARIA scan will be in addition to any standard diagnostic procedures, including imaging, that comprise the standard of care. The scan will require them to lie prone for less than 10 minutes with their breast pendant in an ergonomically-fitted bowl with a thin layer of a coupling fluid (similar to hand moisture in consistency) applied to the surface of the breast.

While there is no direct benefit nor detrimental effect from this study to the patients participating, the study has large implications for many women.

This study will allow the investigators to test the feasibility of this highly innovating approach to breast cancer, with minimal negative effects or possible complications. This diagnostic modality could prove to be a major step forwards in cancer detection, initially as a complementary source of information that can increase confidence in results obtained from established technologies that are routinely deployed in the clinic.

Conditions

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Breast Cancer

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Breast cancer accuracy

Patients with a known or suspected (and subsequently proven) breast cancer

Group Type EXPERIMENTAL

MARIA scan

Intervention Type DIAGNOSTIC_TEST

The patient will have an additional MARIA scan along with conventional imaging, pathology and surgical procedures.

Imaging characteristics and performance

Patients attending the symptomatic clinic

Group Type EXPERIMENTAL

MARIA scan

Intervention Type DIAGNOSTIC_TEST

The patient will have an additional MARIA scan along with conventional imaging, pathology and surgical procedures.

Tumour response in neoadjuvant treatment

Patients who are being treated with neoadjuvant chemotherapy or endocrine treatment

Group Type EXPERIMENTAL

MARIA scan

Intervention Type DIAGNOSTIC_TEST

The patient will have an additional MARIA scan along with conventional imaging, pathology and surgical procedures.

Interventions

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MARIA scan

The patient will have an additional MARIA scan along with conventional imaging, pathology and surgical procedures.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Attending a symptomatic breast care clinic OR Patients who have a diagnosed or suspected breast cancer (P5/M5/U5/B5).
* Female sex
* 18 years or older.
* Able to provide informed consent.
* Not in any identified, vulnerable group.

Exclusion Criteria

* Unable to mount MARIA™ patient bed using provided 2-step
* Unable to lie in the prone position
* Patients who have undergone biopsy less than 5 days before the MARIA™ scan
* Patients with implanted electronics.
* Patients with breast implants.
* Patients with nipple piercings (unless they are removed prior to the MARIA™ scan)
* Breast sizes smaller than 197ml or greater than 1L in volume
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Micrima, Ltd.

INDUSTRY

Sponsor Role collaborator

Royal Marsden NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Steven Allen

Role: STUDY_CHAIR

Royal Marsden NHS Foundation Trust

Richard Sidebottom

Role: PRINCIPAL_INVESTIGATOR

Royal Marsden NHS Foundation Trust

Central Contacts

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Richard Sidebottom

Role: CONTACT

02073528171 ext. 1407

References

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Preece AW, Craddock I, Shere M, Jones L, Winton HL. MARIA M4: clinical evaluation of a prototype ultrawideband radar scanner for breast cancer detection. J Med Imaging (Bellingham). 2016 Jul;3(3):033502. doi: 10.1117/1.JMI.3.3.033502. Epub 2016 Jul 20.

Reference Type BACKGROUND
PMID: 27446970 (View on PubMed)

Saadatmand S, Bretveld R, Siesling S, Tilanus-Linthorst MM. Influence of tumour stage at breast cancer detection on survival in modern times: population based study in 173,797 patients. BMJ. 2015 Oct 6;351:h4901. doi: 10.1136/bmj.h4901.

Reference Type BACKGROUND
PMID: 26442924 (View on PubMed)

Other Identifiers

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CCR4702

Identifier Type: -

Identifier Source: org_study_id