Phototherapy 660 nm for the prevention of radiodermatitis in breast cancer patients receiving radiation therapy: study protocol for a randomized controlled trial
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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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Robijns, Jolien
Censabella, Sandrine
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Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Censabella, Sandrine
Claes, Stefan
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Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Claes, Stefan
Pannekoeke, Luc
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Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Pannekoeke, Luc
Busse, Lore
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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Busse, Lore
Colson, Dora
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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Colson, Dora
Kaminski, Iris
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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Kaminski, Iris
Bulens, Paul
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Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Bulens, Paul
Maes, Annelies
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Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Maes, Annelies
Noe, Leen
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Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Noe, Leen
Brosens, Marc
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Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Brosens, Marc
Timmermans, An
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Jessa Hosp, Dept Dermatol, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Timmermans, An
Lambrichts, Ivo
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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Lambrichts, Ivo
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Somers, Veerle
Mebis, Jeroen
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Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
Jessa Hosp, Dept Med Oncol, Stadsomvaart 11, B-3500 Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Stadsomvaart 11, B-3500 Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium
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Hasselt Univ, Fac Med & Life Sci, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Robijns, J.
Lodewijckx, J.
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Hasselt Univ, Fac Med & Life Sci, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Lodewijckx, J.
Censabella, S.
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Jessa Hosp, Dept Med Oncol, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Censabella, S.
Claes, S.
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Jessa Hosp, Limburg Oncol Ctr, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Claes, S.
Bulens, P.
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Jessa Hosp, Limburg Oncol Ctr, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Bulens, P.
Mebis, J.
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Hasselt Univ, Fac Med & Life Sci, Hasselt, Belgium
Jessa Hosp, Dept Med Oncol, Hasselt, Belgium
Jessa Hosp, Limburg Oncol Ctr, Hasselt, BelgiumHasselt Univ, Fac Med & Life Sci, Hasselt, Belgium