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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05436808
Other study ID # SBU-PCWRT-BREAST
Secondary ID
Status Withdrawn
Phase Early Phase 1
First received
Last updated
Start date July 15, 2022
Est. completion date August 2029

Study information

Verified date October 2023
Source Stony Brook University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The standard treatment for breast cancer when cancer cells were found near or within the margins of the tissue that is removed during breast surgery, is radiation of the entire chest wall. This may be considered overtreatment since the only reason for doing so is that cancer cells were near or in the margins of the breast tissue that was removed. In this study, the amount of radiation treatment will be limited to the area where the remaining cancer cells were found after surgery. The purpose of this study is to find out if partial chest wall radiation therapy is as good as whole chest wall radiation therapy in reducing the risk of breast cancer cancer coming back.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2029
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - DCIS or stage T1 or T2 invasive breast cancer, lymph node negative - Must have undergone mastectomy - Presence of cancer cells on or close to surgical margins - Negative pregnancy test for women - Must receive radiation at Stony Brook University Hospital Exclusion Criteria - Received prior radiation to are to be irradiated

Study Design


Intervention

Radiation:
Partial Chest Wall Radiation Therapy
Patients will receive radiation therapy (30 Gray in 5 fractions) to the affected chest wall, delivered on consecutive days or every other day

Locations

Country Name City State
United States Stony Brook Cancer Center Stony Brook New York

Sponsors (1)

Lead Sponsor Collaborator
Stony Brook University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Breast cancer recurrence Number of patients with recurrent breast cancer 5 years
Primary Acute toxicity Frequency of radiation-related adverse events 3 months
Primary Delayed toxicity Frequency of radiation-related adverse events 5 years
Primary Surgical complications Number of patients with surgical complications 5 years
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