Early-Stage Breast Carcinoma Clinical Trial
Official title:
PICTURE Breast XS: Patient Information Combined for Local Therapy oUtcome Assessment in bREast Cancer - Cross-sectional
This project which is fully funded by the European Union FP7 Program is designed to pull together all the information we obtain from scans and x-rays to design a personalised 3-D digital model of each patient, their anatomy and disease. We can then use this as follows: as (i) an aid to surgical planning to enable objective clinical decision making (ii) a decision support tool to communicate the available treatment options to the patient and facilitate shared decision making and provision of personalised care and (iii) to enable standardised objective evaluation of the aesthetic outcome of the treatment procedures. This study aims to demonstrate the ability of the Virtual Physiological Human concept to empower breast cancer patients and assess the impact on their care and quality of life.
Breast cancer is the most common cancer to affect women in Europe, having a lifetime risk of
1 in 9. It is an increasingly treatable disease, and 10-year survival now exceeds 80%. The
primary treatment for breast cancer is surgery, which may be used in conjunction with
adjuvant therapies, such as chemotherapy and radiotherapy. Given the high breast cancer
survival rate, many women will live for many years with the potentially disfiguring
aesthetic consequences of their surgical and therapeutic treatment. A good aesthetic outcome
is an important endpoint for breast cancer treatment and is closely related to psychosocial
recovery and quality of life.
When a woman faces a breast cancer diagnosis, and surgery is proposed, several options are
available. The decision as to which type of surgery to offer patients is largely subjective
and based almost exclusively on the judgment and experience of the clinician. The cosmetic
outcome of surgery is a function of many factors including tumour size and location, the
volume of the breast, its density, and the dose and distribution of radiotherapy. In
breast-conserving surgery, there is evidence that approximately 30% of women receive a
suboptimal or poor aesthetic outcome; however there is currently no standardised method of
identifying these women.
The PICTURE project aims to address these issues by providing objective tools, tailored to
the individual patient, to predict the aesthetic outcome of local treatment. Using a
combination of 3D photography and routinely acquired radiological images (i.e. mammography,
ultrasound and MRI, when available), together with information about the tumour (size,
location, shape etc.) we will develop techniques to biomechanically model the anatomy of the
breast and the effect of surgical removal of cancerous tissue. This digital patient
representation and associated predictive tools will enable alternative surgical strategies
to be explored and the consequences of the available options, with respect to the appearance
of the breast, to be visualised. This will aid communication with the patient of the type of
breast surgery recommended by the surgeon, and will empower patients to take an active role
in a shared decision making process.
The study will develop tools to enable the patient's aesthetic appearance after treatment to
be objectively evaluated. Current techniques use subjective methods, such as assessment by
an expert panel, or computer analysis of 2-dimensional photography to estimate, for
instance, breast asymmetry. By adopting recent developments in low cost 3D photography and
depth sensing technology, we will develop a standardised, reproducible analysis tool which
will base the aesthetic outcome evaluation on both the 3-dimensional shape of the
reconstructed breast and its volume. This will establish standardised quality assurance and
evaluation procedures, enabling institutions across Europe to be compared and factors that
have a positive or negative impact on surgical outcome identified.
In summary, the demonstrator created by the PICTURE project will integrate models of
surgical techniques and treatment schemes, clinical patient data, multi-modal imaging and
individualised models of patient anatomy to build a personalised, digital representation of
the patient. The aim is for this to be used as an aid to surgical planning, via simulation
of the cosmetic effects of breast conserving surgery, as a decision support tool to
communicate the available options to the patient and to enable standardised evaluation and a
safe outcome of the procedure. The demonstrator aims to empower patients and will have a
direct impact on their care and quality of life.
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