Early-Stage Breast Carcinoma Clinical Trial
Official title:
TARGIT R: TARGeted Intraoperative radioTherapy (TARGIT) Registry Database
This is a prospectively registered database of patients with early breast cancer who will be treated with radiotherapy during surgery. More than 2000 women have already received this treatment in clinical trials. This study will monitor the health status of women who receive this treatment outside of a clinical trial, especially those who might not have been eligible for the original clinical trials. The aim is to confirm the long-term effectiveness and safety of the technique.
Registration of patients selected for this treatment; collecting data regarding safety and
toxicity on patients who have had treatment with TARGIT.
Outcomes will be measured over short and long terms. Outcome measures will include
effectiveness and safety, assessed in various cohorts of patients. Core outcomes will be used
for effectiveness. In addition, true recurrence (basically, ipsilateral breast tumor
recurrence at the same site as the original primary) will be used as defined by Recht. Safety
outcomes will be based on Common Toxicity Criteria.
Budget impact analysis of IORT in subgroups of patients will be assessed. This amounts to
using cost data to calculate the mean incremental (or extra) cost per person treated using
intraoperative radiotherapy (IORT) versus external beam radiotherapy (EBRT) and mastectomies
(where IORT could have been given instead) and then multiplying this by the total patients
eligible nationally for IORT, to calculate the total expected budget impact on the NHS if
IORT in these subgroups was rolled out nationally.
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