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Prospective Assessment of Acute Skin Toxicities in Breast Cancer Patients Undergoing Retreatment with 40 Gy in 15 Fractions Radiation Therapy

Breast Cancer | Radiation Dermatitis

The most common cancer affecting Canadian women is breast cancer, with an estimated 1 in 8 women expected to be diagnosed with breast cancer during their lifetime. Improved screening and treatment have decreased mortality of breast cancer patients, however 14% of cancer-related deaths in Canadian women are still due to breast cancer. Common treatments for breast cancer include surgery, chemotherapy, hormone therapy, and radiation therapy (RT).

Despite recent improvements in treatment and preventative screenings, 20% of breast cancer patients will develop local disease recurrence or another ipsilateral primary breast cancer. . The optimal treatment of recurrent or new primary breast cancers for patients who have undergone prior radiotherapy (RT) is not well-defined. Common treatment approaches consist of mastectomy or a second breast conserving surgery (BCS) with whole or partial breast reirradiation (reRT). In the past, mastectomy has been the preferred treatment for recurrent breast cancer due to concerns over serious acute and late skin toxicities that may result from additional reRT. Many of these late skin toxicities, such as fibrosis, are chronic and can result in patients experiencing pain or other negative impacts to quality of life (QOL).

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Age ≥ 18 years old
* Informed consent
* Histological confirmation of breast malignancy (invasive or in situ carcinoma) or phyllodes
* Previous history of ipsilateral breast cancer treated with RT
* Patients are planned to receive hypofractionated (40Gy/15) RT to the whole or partial breast or chest wall
* Patients treated with or without the addition of a planned boost or bolus
* Patients receiving local or locoregional radiation treatment
* Can communicate in English or be aided by a translator

Exclusion Criteria:

* Patients scheduled to receive conventionally fractionated (50Gy/25 or 45Gy/25) or extreme hypofractionation (26Gy/5)
* Patients planned to receive brachytherapy
* Patients with active rash, pre-existing dermatitis, or other conditions within the treatment area that may make skin assessment for the study difficult per treating physician discretion
* Concomitant cytotoxic chemotherapy
* Scleroderma

Study Location

Odette Cancer Center Sunnybrook Health Sciences Centre
Odette Cancer Center Sunnybrook Health Sciences Centre
Toronto, Ontario
Canada

Contact Study Team

Backup Contact

Edward LW Chow, MBBS

[email protected]
416-480-4974
Primary Contact

Irene Karam, MDCM

[email protected]
416-480-4974
Study Sponsored By
Sunnybrook Health Sciences Centre
Participants Required
More Information
Study ID: NCT06729814