The Use of 3D Surface Imaging in the Objective Assessment of Breast Conserving Therapy

NCT ID: NCT02304614

Last Updated: 2020-10-22

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

Total Enrollment

346 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-04-01

Study Completion Date

2020-12-24

Brief Summary

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3D surface imaging has been used in the objective evaluation of cosmetic outcome of oncoplastic procedures such as breast reconstruction and lipofilling, however there is only one article published relating to Breast Conserving Therapy (BCT).

The aim of this study is to assess the use 3D surface imaging as a tool in the assessment of symmetry of outcome following breast conserving therapy. The results of the surface imaging will be correlated with patient satisfaction, using the BREAST-Q, which is a validated patient questionnaire and correlated with panel assessment by an independent panel of two surgeons, one clinical oncologist and one breast care nurse.

Detailed Description

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BCT is the most common breast surgical oncological procedure performed with approximately 28,500 patients undergoing this operation every year. In breast cancer surgery, the primary aim of removing the cancer must be reconciled with the secondary aim of preserving breast aesthetics. Objective analysis of cosmetic outcome measures in breast surgery has been lacking, however 3D surface imaging is beginning to show promise in this area. Having a robust tool for objective assessment of outcomes may facilitate critical appraisal of techniques and therefore surgeon learning.

Currently the cosmetic success of an operation can be subjectively evaluated by patients' and surgeons' visual assessment. Patient reported outcome measures (PROMs) are instruments to measure any aspect of a patient's health status. Various PROMs have been used to evaluate patients' satisfaction after breast cancer treatment. For example, the BREAST-Q was developed quantitatively and qualitatively to measure patients' perceptions before and after breast reconstruction by examining quality of life domains (psychosocial well-being, physical well-being, sexual well-being) and satisfaction domains (satisfaction with breasts, satisfaction with outcome, satisfaction with care). When using any of these PROMs, accuracy and reproducibility are not measurable; the results are the subjective views of the patient. While the patient opinion of her own appearance is clearly the most important outcome after local oncological control, for the purposes of objective comparison between groups of patients, surgeons and over time, independent clinicians (and / or lay people) may be recruited to perform a 'panel assessment' of photographs in which the various aspects of cosmesis such as breast shape, size and cleavage are considered in addition to overall appearance. However such assessments are still subjective and often lack accuracy and reproducibility.

There have been many attempts to derive objective measures of outcome. In the 1970's, Edstron et al described 'split and reversed negatives' where photographic negatives of the left and right breast were made and laid next to the non-negative right and left breast. The constructed images of perfectly symmetrical breasts were compared with the original photographs of the patients' breasts. More recently two software systems have been developed to objectively evaluate the aesthetic surgical outcomes of breast surgery using 2D photographs. The Breast Analyzing Tool (BAT©) evaluates symmetry by comparing breast area, breast circumference and nipple position between the breasts. The Breast Cancer Conservative Treatment cosmetic result (BCCT.core) also analyses colour differences and the scar appearance in addition to asymmetry calculations.

The use of 3D surface imaging in the clinical setting was first described by Burke and Beard in 1967 to analyze facial structures. Over the last fifteen years 3D imaging has been used as a research and clinical tool in aesthetic, oncoplastic and reconstructive breast surgery. Initial studies established optimal technique to obtain images and tested accuracy and reproducibility. 3D imaging is currently used to simulate for the patient what a cosmetic augmentation might achieve in terms of size and shape. It has been demonstrated that simulated images are accurate and patients felt they helped them to choose the implant.

In terms of oncoplastic reconstructive surgery 3D surface imaging has been used in the objective evaluation of cosmetic outcome of oncoplastic procedures such as breast reconstruction and lipofilling, however there is only one article published relating to Breast Conserving Therapy (BCT). Moyer et al analyzed twenty three patients who had undergone BCT and compared volume and asymmetry. They found that there was a positive correlation between percentage of breast parenchyma excised and asymmetry. The location of the cancer, age of the patient and need for multiple operations did not influence cosmetic results but the sample size was small and therefore likely underpowered.

The aim of this study is to assess the use 3D surface imaging as a tool in the assessment of symmetry of outcome following breast conserving therapy. The results of the surface imaging will be correlated with patient satisfaction, using the BREAST-Q, which is a validated patient questionnaire and correlated with panel assessment by an independent panel of two surgeons, one clinical oncologist and one breast care nurse.

Conditions

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Breast Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Group 1

Patients who have undergone Breast conserving Therapy

3D surface imaging using a non portable and portable camera

Intervention Type OTHER

The participant will have 3D surface imaging taken of their breasts (the face will not be shown)

Patient reported outcome measure (PROM): BREAST-Q

Intervention Type OTHER

The participant will answer the BREAST-Q questionnaire. This is a patient reported outcome measurement of satisfaction and quality of life after BCT

2D photography

Intervention Type OTHER

The participant will have standard medical photography of their breasts (the face will not be shown)

Applanation Tonometry

Intervention Type OTHER

A small 300g disc is placed on the breast to measure the surface area of contact with the breast to measure compressibility

Interventions

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3D surface imaging using a non portable and portable camera

The participant will have 3D surface imaging taken of their breasts (the face will not be shown)

Intervention Type OTHER

Patient reported outcome measure (PROM): BREAST-Q

The participant will answer the BREAST-Q questionnaire. This is a patient reported outcome measurement of satisfaction and quality of life after BCT

Intervention Type OTHER

2D photography

The participant will have standard medical photography of their breasts (the face will not be shown)

Intervention Type OTHER

Applanation Tonometry

A small 300g disc is placed on the breast to measure the surface area of contact with the breast to measure compressibility

Intervention Type OTHER

Other Intervention Names

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3D photography medical photography Measurement of breast compressibility

Eligibility Criteria

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Inclusion Criteria

* Female patients
* No age limit
* underwent unilateral breast conserving surgery at The Royal Marsden NHS Foundation Trust (RMH)
* underwent adjuvant whole breast radiotherapy at RMH
* attending for their annual surveillance mammogram
* between one and five and half years after surgery (rounded to nearest whole year)

Exclusion Criteria

* undergone surgery to the contralateral breast (breast conserving surgery, symmetrisation or mastectomy)
* undergone further surgery to the affected breast subsequent to BCT (eg lipofilling or other reconstruction).
* unable to stand for long enough to have clinical photos (approximately 10 minutes)
* unable to answer the BREAST-Q questionaire (e.g. learning difficulties)
Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Royal Marsden NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jennifer E Rusby, DM FRCS

Role: PRINCIPAL_INVESTIGATOR

Royal Marsden NHS Foundation Trust

Locations

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The Royal Marsden NHS Foundation Trust

Sutton, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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CCR4252

Identifier Type: -

Identifier Source: org_study_id

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