Intraoperative Radiation Therapy (IORT) Following Breast Conserving Surgery for Early Stage Breast Cancer Registry

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Observational
SUMMARY

This is a prospective, registry trial which will enroll women aged 65 and above with early stage, low risk breast cancer who will be treated with partial mastectomy and intraoperative radiation therapy (IORT). The primary aim is to determine the 5-year risk of in-breast tumor recurrence. Secondary aims include identification of acute- and late-toxicity, cosmetic result, disease-free survival and overall survival.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 65
Healthy Volunteers: f
View:

• Female

• ECOG performance status 0-1

• Age 65 years or older

• cT1 or cT2 (≤3.0 cm)

• Invasive ductal carcinoma histology

• Estrogen receptor positive (ER+)

• Grade 1 or Grade 2

• Clinically negative lymph nodes (cN0) by examination, imaging and/or nodal sampling

• Suitable for breast conserving surgery and radiation therapy

• Patient must be able to provide study-specific informed consent

Locations
United States
Ohio
Mount Carmel West Hospital
RECRUITING
Columbus
Contact Information
Primary
Lynn Shaffer, PhD
Lynn.Shaffer@mchs.com
614-234-3625
Time Frame
Start Date: 2018-02-27
Estimated Completion Date: 2028-02-27
Participants
Target number of participants: 168
Treatments
IORT
All patients will undergo a partial mastectomy with sentinel lymph node biopsy with the goal of achieving a margin-negative resection while maintaining good cosmetic outcome. Immediately following partial mastectomy and frozen section evaluation of the sentinel lymph nodes, IORT is to be delivered. Intraoperative radiation therapy will involve 50 kV xrays to a dose of 20 Gy during breast conserving surgery. After surgery, patients are followed based on the standard schedule determined by their surgeon for 5 years.
Related Therapeutic Areas
Sponsors
Leads: Mount Carmel Health System

This content was sourced from clinicaltrials.gov