Impact of Individualized Radiotherapy Plan Review in Patients Receiving Adjuvant Radiotherapy for Breast Cancer



Status:Recruiting
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 100
Updated:5/10/2018
Start Date:April 2014
End Date:February 2027
Contact:Jyoti Mayadev, MD
Email:jyoti.mayadev@ucdmc.ucdavis.edu
Phone:916-724-8269

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This study is being conducted to investigate the effect of a more in-depth education plan for
patients with breast cancer. Patients will be randomized to receive either the standard
education plan during their breast cancer treatment or they will receive in-depth education
about their breast cancer treatment. In order to see what kind of effect the different
education plans have, patients will fill out three identical questionnaires during the course
of treatment.

This study will be a prospective study of women receiving adjuvant radiation therapy for
management of breast cancer at the University of California Davis. All patients will be
staged according to the American Joint Committee on Cancer Seventh edition. Primary disease
treatment information including surgical approach and utilization of adjuvant chemotherapy
will be evaluated.

All patients will have a validated quality of life assessment (FACIT-TS-PS) completed at
three time points during their radiation therapy process. The patients will be randomized at
the time of completion of radiation plan approval by the treating radiation oncologist in a
one to one fashion to either proceed with standard education or more extensive plan review.
The radiation oncology quality assurance (QA) process will be blinded to the randomization of
the patient.

Inclusion Criteria

1. Diagnosis of invasive breast cancer

2. AJCC stage 1, 2, 3 breast carcinoma

3. Patient deemed clinically appropriate for adjuvant breast or chest wall radiation
following surgery

4. Women of childbearing potential must be non-pregnant and non-lactating and willing to
use medically acceptable form of contraception during radiation therapy

5. Patient must provide study specific informed consent prior to study entry

6. Breast implants allowed

Exclusion Criteria

1. Stage 4 breast cancer

2. Ductal carcinoma in situ

3. Patients treated with radiation for palliative intent

4. Prior treatment with radiation therapy to the ipsilateral breast or chest wall

5. Prior invasive non-breast malignancy (except non-melanomatous skin cancer, carcinoma
in situ of the cervix) unless disease free for a minimum of 5 years prior to study
entry

6. Prior invasive or in-situ carcinoma of the breast (-prior LCIS is eligible)

7. Diagnosis of DCIS
We found this trial at
1
site
Sacramento, California 95814
Principal Investigator: Jyoti Mayadev, MD
?
mi
from
Sacramento, CA
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