Quantifying Radiation-Induced Skin Reactions: Establishing the Foundation for Future Prediction Models
Study Details
Study Description
Brief Summary
Breast cancer has the highest incidence rate among female cancers, and breast radiotherapy plays an essential role in the treatment of breast cancer. However, the acute and chronic skin reactions caused by radiotherapy, especially radiation dermatitis, have a significant impact on the physical and mental health of breast cancer patients. Severe acute radiation dermatitis can affect the patient's quality of life and may even lead to treatment interruption, thereby affecting treatment efficacy. Chronic radiation dermatitis can lead to irreversible skin problems, such as "radiation-irritated skin" and skin pigmentation, which can affect the quality of life of breast cancer patients after treatment.
This study aimed to evaluate and examine the skin reactions of 30 breast cancer patients who underwent whole-breast radiotherapy after breast conserving surgery. The subjects returned to the hospital for evaluation every week during radiotherapy, and in the second and sixth weeks after the end of the treatment, they received physical examinations and surveys, including questionnaire surveys, skin observations and measurements. The study lasted for 3 months. Skin observation items included physiological parameters such as skin moisture, temperature, melanin, transepidermal water loss (TEWL), and clinical evaluation of skin reactions by physicians. Through statistical analysis of skin physiological parameters, scientific instruments can quantify the radiation skin reactions traditionally judged by clinical physicians by visual examination and can perform real-time clinical prediction monitoring, which can be used to establish a skin reaction prediction model in the future.
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Study Design
Outcome Measures
Primary Outcome Measures
- The worst skin toxicity according to CTCAE grading. [1-Week (Day0), 2-Week (Day7), 3-Week (Day14), 4-Week (Day21), 5-Week (Day28), 6-Week (Day35), Post-radiotherapy 2 Week later]
The worst skin toxicity during radiotherapy and 2 weeks after according to CTCAE grading.
Secondary Outcome Measures
- To compare the skin moisture percentage. [1-Week (Day0), 3-Week (Day14), 5-Week (Day28), 6-Week (Day35), Post-radiotherapy 2 Week later, Post-radiotherapy 6 Week later]
To compare the skin moisture percentage at the radiotherapy site and normal site from baseline to follow-up visit.
- To compare the skin trans-epidermal water loss. [1-Week (Day0), Post-radiotherapy 2 Week later, Post-radiotherapy 6 Week later]
To compare the skin trans-epidermal water loss at the radiotherapy site and normal site from baseline to follow-up visit.
- To compare the skin temperature of target region. [1-Week (Day0), 3-Week (Day14), 5-Week (Day28), 6-Week (Day35), Post-radiotherapy 2 Week later, Post-radiotherapy 6 Week later]
To compare the skin temperature of target region at the radiotherapy site and normal site from baseline to follow-up visit.
- The score of quality of life with the Skindex-16 questionnaire performed every two weeks. [1-Week (Day0), 3-Week (Day14), 5-Week (Day28), 6-Week (Day35), Post-radiotherapy 2 Week later, Post-radiotherapy 6 Week later]
The score of quality of life with the Skindex-16 questionnaire performed every two weeks.
- Median time to G2 radiation dermatitis development [1-Week (Day0), 2-Week (Day7), 3-Week (Day14), 4-Week (Day21), 5-Week (Day28), 6-Week (Day35), Post-radiotherapy 2 Week later, Post-radiotherapy 6 Week later]
Median time to G2 radiation dermatitis development
Eligibility Criteria
Criteria
Inclusion Criteria:
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Participants must be males or non-pregnant females at least 18 years of age.
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Diagnosis of non-inflammatory breast adenocarcinoma or in situ breast cancer which will be treated by radiotherapy after operation.
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Patient had unilateral breast conservation surgery with or without adjuvant or neoadjuvant chemotherapy or hormonal treatment.
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Patients were scheduled to receive at least five sessions of radiotherapy per week (1 session per day) for at least four weeks using standard irradiation fraction (with at least 1.8 Gy per session) for total dose of at least 45 Gy.
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Participant must give informed consent.
Exclusion Criteria:
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Bilateral breast cancer
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Previous radiotherapy to the chest
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Prior breast reconstructions, implants, and/or expanders
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Known radiosensitivity syndromes (e.g. Ataxia-telangiectasia)
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Collagen vascular disease, vasculitis, unhealed surgical sites, breast infections or systemic lupus erythematosus (SLE)
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Participation in any clinical trial in the prior 30 days from baseline.
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Any condition that, in the judgement of the investigator could impose hazards to the patient if study therapy is initiated or affect the participation of the patient in the study.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- China Medical University Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CMUH112-REC1-120