Breast Cancer
Conditions
Brief summary
Prospective single centre study of patients with DCIS that have undergone breast conservation surgery.
Detailed description
This is a single centre (Royal Marsden Hospital - Chelsea and Sutton) non-randomised trial investigating whether the Oncotype DX DCIS score changes the radiotherapy recommendation made by clinical oncologists in patients with low to moderate risk DCIS following breast conserving surgery.
Interventions
DIAGNOSTIC_TESTONCOTYPE DX DCIS test
The Oncotype DX DCIS score, comprised of 12 of the 21 genes of the Oncotype DX Recurrence score, has been developed by Genomic Health Inc. Two clinical utility studies have now been performed in USA, assessing the value of the Oncotype DX DCIS to clinical decision making (18,19) The first study by Alvarado et al. evaluated the influence of the test in 10 centres and in 115 patients (18). The DCIS score led to a change in the treatment recommendation in 36 patients (31.3%; 26 patients had a change to no radiation and 10 patients had a change to recommend radiation). The second study similarly showed change in recommendations following the Oncotype DX DCIS test in 26.4% of cases. It is unclear what the impact of the DCIS score test would be in the UK.
Sponsors
Royal Marsden NHS Foundation Trust
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
1. Confirmed diagnosis of DCIS 2. DCIS treated with breast conserving surgery
Exclusion criteria
1. Prior treatment for DCIS or invasive breast cancer in ipsilateral breast. 2. Patients with contra-indications to radiotherapy, including prior breast radiotherapy 3. Patients who undergo mastectomy for DCIS 4. Age \< 45 years old 5. Patients with \> 25mm DCIS 6. Patients with multifocal DCIS (defined as more than 1 distinct focus of DCIS with at least 50mm of intervening benign tissue) 7. Patients with invasive (including microinvasion) disease 8. Patients with positive axillary nodal disease (including isolated tumour cells) 9. Patients with close (\<1mm) or positive radial margins (unless maximally surgically excised or no further DCIS on re-excision) 10. Patients recommended adjuvant endocrine therapy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in radiotherapy recommendation by clinician | end of trial (2 years) | Percentage of clinical oncology recommendations regarding radiotherapy that change pre- and post- Oncotype DX DCIS. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Determine whether the local recurrence risk estimated by clinical oncologists agrees with the local recurrence risk calculated by the Oncotype DX DCIS score (for all recurrences and for invasive recurrences only). | end of trial (2 years) | Agreement between the local recurrence risk estimated by clinical oncologists and the local recurrence risk calculated by the Oncotype DX DCIS score (for all recurrences and for invasive recurrences only). |
| Determine change in patient decisional conflict pre and post Oncotype DX DCIS. | end of trial (2 years) | Change in patient decisional conflict scale (DCS) scores pre and post Oncotype DX DCIS |
| Determine change in patient anxiety pre and post Oncotype DX DCIS. | end of trial (2 years) | Change in state anxiety and trait anxiety scores using the State Trait Anxiety Inventory (STAI) pre and post ONCOTYPE DX DCIS test |
| Determine whether the Oncotype DX DCIS score results in a change in patient decision for adjuvant radiotherapy. | end of trial (2 years) | Percentage of patients who change their decision regarding radiotherapy pre- and post- Oncotype DX DCIS. |
| Determine patient, tumour and clinician related factors that are associated with patients changing their decision regarding radiotherapy. | end of trial (2 years) | Patient, tumour and clinician related factors (data collected during Visit 1) that are associated with patients changing their decision regarding radiotherapy. |
| Determine patient, tumour and clinician related factors that are associated with patients' final decision to have radiotherapy. | end of trial (2 years) | Patient, tumour and clinician factors that are associated with patients' final decision to have radiotherapy. |
| Determine patient, tumour and clinician factors that are associated with clinicians changing their decision regarding radiotherapy. | end of trial (2 years) | Patient, tumour and clinician factors (data collected during Visit 1) that are associated with clinicians changing their decision regarding radiotherapy. |
Countries
United Kingdom
Outcome results
None listed