Breast Cancer Clinical Trial

Hypofractionated Radiotherapy in Breast Cancer

Summary

As the number of breast cancer (BrCA) survivors has markedly increased, clinicians are now seeking to reduce treatment-related toxicities and inconveniences of treatment, namely the traditional 6 weeks of daily radiation treatment (XRT). Skin thickening, fibrosis, and edema are some of the most common acute and potentially long-term debilitating toxicities of BrCA XRT.

The purpose of this study is to learn if three weeks of daily radiation treatment (RT) to the breast is safe in breast cancer patients who are usually prescribed 6 weeks of daily radiation after breast surgery (e.g. lumpectomy or mastectomy) as standard of care.

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Full Description

As the number of breast cancer (BrCA) survivors has markedly increased, clinicians are now seeking to reduce treatment-related toxicities and inconveniences of treatment, namely the traditional 6 weeks of daily radiation treatment (XRT). Skin thickening, fibrosis, and edema are some of the most common acute and potentially long-term debilitating toxicities of BrCA XRT.

The purpose of this study is to learn if three weeks of daily radiation treatment (RT) to the breast is safe in breast cancer patients who are usually prescribed 6 weeks of daily radiation after breast surgery (e.g. lumpectomy or mastectomy) as standard of care.

Investigators seek to assess the rate of cutaneous toxicity, the rates of lymphedema determined by arm measurements and Grade 3 brachial plexopathy in patients receiving regional nodal irradiation, as well as local control, quality of life, and fatigue levels.

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Eligibility Criteria

Inclusion Criteria:

Participants must have one or more of the following characteristics and be eligible for breast or chest wall with or without regional nodal radiotherapy:

Prior Chemotherapy for Breast Cancer
Greater than 25 cm of breast separation (the largest distance on an axial slice of the planning CT simulation scan between the entry and exit points of the radiation beam on the body)
Non-Caucasian Race
Less than or equal to 50 years of age
Requiring regional nodal irradiation without evidence of N3 disease

Exclusion Criteria:

Males will be excluded
Women who are pregnant or nursing a child may not take part in this study

Study is for people with:

Breast Cancer

Estimated Enrollment:

74

Study ID:

NCT03167359

Recruitment Status:

Completed

Sponsor:

Emory University

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There is 1 Location for this study

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Emory University
Atlanta Georgia, 30322, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

74

Study ID:

NCT03167359

Recruitment Status:

Completed

Sponsor:


Emory University

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