Participant must have histologically or cytologically confirmed stage 0 ductal carcinoma in situ (DCIS), I, II or III breast cancer and be planning to undergo radiation therapy (RT) after surgery
Participants must be 18 years of age or older
Participant must be able to understand a written informed consent document and be willing to sign it
Participant must be assigned female at birth
Participant must have a Karnofsky performance score of greater than or equal to 70%
Women of child bearing potential must agree to avoid becoming pregnant through defined periods during the course of RT and must meet one of the following:
* Surgically sterile (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy
* Post-menopausal, defined as no menses for at least 12 months prior to the screening visit without alternative medical causation
* Agree to practice true abstinence from sexual intercourse
* Not in a sexual relationship in which the may become pregnant (i.e., same-sex relationship)
* If they are childbearing potential, agree to use at least one highly effective and at least one additional method of contraception.
For the first six participants only: Participant must have a Fitzpatrick Skin Tone Scale of 5 or 6
You may not be if
Participants who have received prior radiation treatment to the affected breast.
Participants with a history of allergic reaction or hypersensitivity attributed to any tattoo ink
Participants with active chronic skin diseases such as psoriasis. Participants with inactive or controlled skin diseases are eligible for this study
Participants that are pregnant or breastfeeding. If a participant wishes to participate in this study, breastfeeding should be discontinued
Participants with a BMI greater than 44.5 as calculated within six months prior to the starting of the study. If there are multiple BMI measurements available in the chart, the most recent will be used to determine eligibility.
