Phototherapy 660 nm for the prevention of radiodermatitis in breast cancer patients receiving radiation therapy: study protocol for a randomized controlled trial

被引:20
|
作者
Costa, Marina Moreira [1 ]
Silva, Sidney Benedito [2 ]
Pereira Quinto, Ana Luiza [3 ]
Souza Pasquinelli, Priscilla Furtado [4 ]
dos Santos, Vanessa de Queiroz [2 ]
Santos, Gabriela de Cassia [2 ]
Veiga, Daniela Francescato [5 ,6 ]
机构
[1] Hosp Canc Barretos, Dept Oncol, BR-14784400 Barretos, SP, Brazil
[2] Univ Vale Sapuca, Dept Physiotherapy, BR-37550000 Pouso Alegre, MG, Brazil
[3] Hosp Canc Barretos, Dept Radiotherapy, BR-14784400 Barretos, SP, Brazil
[4] Oncominas, Dept Radiotherapy, BR-37550 Pouso Alegre, MG, Brazil
[5] Univ Vale Sapuca, Dept Plast Surg, BR-37550000 Pouso Alegre, MG, Brazil
[6] Univ Fed Sao Paulo, Dept Plast Surg, BR-04024002 Sao Paulo, Brazil
关键词
Breast neoplasms; Laser therapy; Low-level; Radiodermatitis; Prevention & control; LEVEL LASER THERAPY; HE-NE-LASER; POSTMASTECTOMY LYMPHEDEMA; INDUCED MUCOSITIS; SKIN REACTIONS; MANAGEMENT; DERMATITIS;
D O I
10.1186/1745-6215-15-330
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Breast neoplasms are the second most common type of cancer worldwide, and radiation therapy is a key component of their treatment. Acute skin reactions are one of the most common side effects of radiation therapy, and prevention of this adverse event has been investigated in several studies. However, a clinically applicable, preventative treatment remains unavailable. It has been demonstrated that application of a low-power laser can promote tissue repair. Therefore, the aim of this trial is to evaluate the effectiveness of an indium gallium aluminum phosphorus (InGaAIP) laser operated at 660 nm in preventing radiodermatitis in women undergoing adjuvant radiotherapy for breast cancer. Methods/Design: This is a two-arm, randomized controlled trial. A total of 52 patients undergoing radiotherapy for breast cancer (stages I to III) will be enrolled. Patients will be randomly assigned to an intervention group to receive laser therapy (n = 26) or a control group to receive a placebo (n = 26). The laser or placebo will be applied five days a week, immediately before each radiotherapy session. Skin reactions will then be graded weekly by a nurse, a radiotherapist, and an oncologist (all of whom will be blinded) using the Common Toxicity Criteria (CTC) developed by the National Cancer Institute and the Acute Radiation Morbidity Scoring Criteria developed by the Radiation Therapy Oncology Group. Patients will also answer a modified visual analogue scale for pain (a self-evaluation questionnaire). Primary and secondary outcomes will be the prevention of radiodermatitis and pain secondary to radiodermatitis, respectively. Discussion: The ideal tool for preventing radiodermatitis is an agent that mediates DNA repair or promotes cell proliferation. Application of a low-power laser has been shown to promote tissue repair by reducing inflammation and inducing collagen synthesis. Moreover, this treatment approach has not been associated with adverse events and is cost-effective. Thus, the results of this ongoing trial may establish whether use of a low-power laser represents an ideal treatment option for the prevention of radiodermatitis.
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页数:6
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