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Status unknownNCT03302819LIESLUpdated Oct 5, 2017

London Investigation Into diElectric Scanning of Lesions

An interventional study of MARIA scan in Breast Cancer, sponsored by Royal Marsden NHS Foundation Trust. Status unknown. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-10-05.

Sponsored by Royal Marsden NHS Foundation Trust · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Sep 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
994
Allocation
Non-randomized
Ages
18 Years and older
Sex
Female
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Study summary

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.

Read the detailed description

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.

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Conditions studied

  • Breast Cancer

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03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

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

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
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
994 participants (estimated)

Study arms

  • Experimental
    Breast cancer accuracy

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

    Diagnostic Test: MARIA scan

  • Experimental
    Imaging characteristics and performance

    Patients attending the symptomatic clinic

    Diagnostic Test: MARIA scan

  • Experimental
    Tumour response in neoadjuvant treatment

    Patients who are being treated with neoadjuvant chemotherapy or endocrine treatment

    Diagnostic Test: MARIA scan

Interventions

  • Diagnostic testMARIA scan

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

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What researchers measure

Primary outcomes

  1. Proportion of patients with breast cancer in whom breast cancer is correctly identified by MARIA

    Comparison to histopathology result

    Time frame: 1 week (after histopathology result)

  2. Sensitivity and specificity of MARIA for a range of findings to include, simple cysts, fibroadenomata, and malignant lesions. As judged against the final diagnosis at discharge, which may be based on clinical findings, imaging and pathology data.

    Comparison with clinical, radiology and pathology findings

    Time frame: Through study completion, an average of 1 year

  3. Proportion of post-operative patients treated with neo-adjuvant chemotherapy or endocrine therapy, correctly identified by MARIA with complete response or residual disease, as compared to surgical histology.

    Comparison of response to surgical histology

    Time frame: Through study completion, an average of 1 year

Secondary outcomes

  1. Compare the detection of breast cancer from MARIA with the detection from mammography by the sub-group of histology type.

    Comparison to Mammography and Pathology result

    Time frame: Through study completion, an average of 1 year

  2. Compare the detection of breast cancer from MARIA with the detection from mammography by sub-group of mammographic density.

    Comparison to Mammography and Pathology result

    Time frame: Through study completion, an average of 1 year

  3. Compare the detection of breast cancer from MARIA with the detection from mammography in the overall patient group.

    Comparison to Mammography and Pathology result

    Time frame: Through study completion, an average of 1 year

  4. Assessment of data repeatability (test re-test) of MARIA assessment results on patients with diagnostic follow-up imaging.

    Comparison with prior MARIA scan when returning for further imaging

    Time frame: After attendance for further imaging, at 1-2 weeks.

  5. Investigate the performance of MARIA in the estimation of residual tumour size compared to the final surgical histology results in the case of patients receiving neo-adjuvant chemotherapy or endocrine therapy.

    The correlation between the pathological features of the lesion and the imaging features as determined from MARIA including presence of features, shape and size.

    Time frame: Through study completion, an average of 1 year

  6. Patient tolerance of MARIA (a non-compressing, non-ionising modality)

    Questionnaire measurement, Quantitative answers.

    Time frame: Through study completion, an average of 1 year

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • 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. PubMed 27446970 ↗
  • 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. PubMed 26442924 ↗

Individual participant data

Plan to share: No

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Registry details

Key details

Study ID
NCT03302819
Lead sponsor
Royal Marsden NHS Foundation Trust
Collaborators
Micrima, Ltd.
Responsible party
Sponsor
First posted
Oct 5, 2017
Start date
Nov 1, 2017 (estimated)
Primary completion
Nov 1, 2018 (estimated)
Completion
Dec 1, 2018 (estimated)
Last update
Oct 5, 2017

Study contacts

Richard Sidebottom
Contact
richardsidebottom@nhs.net
02073528171 ext. 1407
Steven Allen
study chair · Royal Marsden NHS Foundation Trust
Richard Sidebottom
principal investigator · Royal Marsden NHS Foundation Trust

Oversight

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

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This study is status unknown, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

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