Evaluation of Radiobiological Effects in Skin Toxicities for Breast Cancer Patients With Pencil Beam Scanning Proton Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCovenant Health Cancer Center

About this trial

This purpose of this study is to examine skin reactions (called radiation dermatitis) that occur during pencil beam scanning (PBS) proton therapy. The researchers will test a unique technique called "Spot Delete" to see if it can reduce skin reactions for breast patients treated with PBS. They will also use a special computer model to study how the energy of the proton beam (linear energy transfer) is related to these skin reactions. The study involves creating a treatment plan based on a CT scan, which helps guide the proton beam in the body. The clinical team uses this CT scan to find the best placement for the protons. The "Spot Delete" method prevents protons from stopping in the skin, which is thought to cause skin redness.

Eligibility criteria

Qualifiers

The patient must consent to be in the study and must have signed an approved consent form conforming to federal and institutional guidelines.

Patients must be equal to or greater than 18 years old.

The patient must have stage 0, I, II, or III breast cancer

On histological examination, the tumor must be ductal carcinoma in-situ (DCIS) or invasive adenocarcinoma of the breast

Disqualifiers

Stage IV breast cancer

Non-epithelial breast malignancies such as sarcoma or lymphoma

Paget's disease of the nipple

Prior breast or thoracic radiation therapy (RT) for any condition.

Trial design

Treatments tested in this trial

  • Pencil Beam Scanning Proton Therapy

Treatment groups

No treatment groups listed

Sponsors and collaborators