- Study protocol
- Open Access
Preventing the acute skin side effects in patients treated with radiotherapy for breast cancer: the use of corneometry in order to evaluate the protective effect of moisturizing creams
Radiation Oncologyvolume 8, Article number: 57 (2013)
Background and purpose
The purpose of this study was to add, to the objective evaluation, an instrumental assessment of the skin damage induced by radiation therapy.
Materials and methods
A group of 100 patients affected by breast cancer was recruited in the study over one year. Patients were divided into five groups of 20 patients. For each group it was prescribed a different topical treatment. The following products were used: Betaglucan, sodium hyaluronate (Neoviderm®), Vitis vinifera A. s-I-M.t-O.dij (Ixoderm®), Alga Atlantica plus Ethylbisiminomethylguaicolo and Manganese Cloruro (Radioskin1®) and Metal Esculetina plus Ginko Biloba and Aloe vera (Radioskin 2®); Natural triglycerides-fitosterols (Xderit®); Selectiose plus thermal water of Avene (Trixera+®). All hydrating creams were applied twice a day starting 15 days before and one month after treatment with radiations. Before and during treatment patients underwent weekly skin assessments and corneometry to evaluate the symptoms related to skin toxicity and state of hydration. Evaluation of acute cutaneous toxicity was defined according to the RTOG scale.
All patients completed radiotherapy; 72% of patients presented a G1 cutaneous toxicity, 18% developed a G2 cutaneous toxicity, 10% developed a G3 toxicity, no one presented G4 toxicity. The corneometry study confirmed the protective role of effective creams used in radiation therapy of breast cancer and showed its usefulness to identify radiation-induced dermatitis in a very early stage.
The preventive use of topic products reduces the incidence of skin side effects in patients treated with radiotherapy for breast cancer. An instrumental evaluation of skin hydration can help the radiation oncologist to use strategies that prevent the onset of toxicity of high degree. All moisturizing creams used in this study were equally valid in the treatment of skin damage induced by radiotherapy.
The most important aspects in the management of radiation–induced skin reactions are prophylaxis and, when they appear, their appropriate treatment. Breast cancer has an high incidence rates in Italy, and it is the first cause of cancer death in women . Screening programs increased the diagnosis of breast tumors in the initial stage and then survival . Every year about 35,000 new cases are diagnosed and 80% of these being treated in Italian Radiotherapy Centers . A great number of patients are submitted to adjuvant radiotherapy after surgery with or without chemotherapy. In the course of radiotherapy, skin toxicity remains an important clinical problem for many patients. The severity of the acute toxicity is related to several factors: dose per fraction, total delivered dose, location and volume of the treated area, radiating energy, other treatments received concomitantly or before. The literature shows individual variations depending on age, chronic diseases, skin types, genetic predisposition, skin damage from the previous and concomitant drug therapy (cytotoxic chemotherapy) [4, 5].
However, it is difficult to estimate the frequency and intensity of these adverse effects. Temporary skin reactions vary from mild erythema to brisk moist desquamation. At present, guidelines regarding skin care during the course of radiotherapy remain inconsistent. Moreover all treatments remain linked to a subjective evaluation of the patient that the specialist involved (Dermatologist, Radiation Oncologist, Surgeon or Medical Oncologist) performs, in the majority of cases without a multidisciplinary evaluation .
Our treatment policies provide a prophylactic use of a topical therapy to prevent skin damages. The purpose of this study was to add to the subjective evaluation of the topical therapy, an instrumental measurement for the assessment of skin damage induced by radiation therapy.
Methods and material
From January 2011 to December 2011 we enrolled a group of 100 consecutive female patients, aged from 29 to 75 years (median age 59) with a pathologic diagnosis of breast cancer. Were included in the study patients treated with conservative surgery (quadrantectomy), surgical margins were free of disease, and there wasn’t indication for regional nodal radiation therapy (less than four nodes involved) according to our national guidelines . Therefore they were candidates for adjuvant radiotherapy with 6 MV photons, with a dose of 50 Gy (2Gy/fraction) to whole breast with tangential fields, and a subsequent additional dose of 10 Gy (2Gy/fraction) to the tumor bed . All patients were submitted to a simulation Simulation CT-Scan, the three-dimensional treatment plan was set with the Pinnacle® TPS system, the target volumes were delineated according to the criteria of the International Commission on Radiation Units [9, 10].
In our Department is active from 2010 a multidisciplinary ambulatory in which Dermatologists and Radiation Oncologists can visit the patients at the same time.
In Table 1 shows the characteristics of the patients.
Patients were randomized into five groups. Each group received the prescription of a prophylactic moisturizing cream.
Topical treatments prescribed to five groups were as follows:
Group A = Betaglucan, sodium hyaluronate (Neoviderm®)
Group B = Vitis vinifera A. s-I-M.t-O.dij (Ixoderm®)
Group C = Alga Atlantica and ethylbisiminomethylguaicolo Manganese Cloruro (Radioskin 1®) and metal esculetina, ginko biloba and Aloe vera (Radioskin 2®)
Group D = Natural triglycerides-fitosterols (Xderit®)
Group E = Selectiose, thermal water of Avene (Trixera+®)
Patients were evaluated, with corneometry, by dermatologists before and during radiotherapy and clinically together with radiation oncologists. At that moment of the CT Simulation they were instructed to apply cream topically every day (2–3 times/day) before (least 3 hours before) and after the radiotherapy treatment. They started radiation therapy medially 15 days after the beginning of the topical treatment and it was indicate to use the products also 1 month after the end of treatment. Moreover, during radiotherapy it was prohibited to use other types of creams or perfumes on the irradiated skin. Patients were asked not to apply the creams within 3 hours before radiation treatment and were educated to carefully wash the area only with special oil soap and to wear loose clothes, preferably made of cotton.
The patients were subjected to clinical examination plus Corneometry: 1) at the time of CT simulation, and 2) every week during treatment and 3) 1 month after the end of therapy. The evaluation was carried out jointly by the radiation oncologist and dermatologist. The radiation oncologist evaluated the radiodermatitis, according to the RTOG scale, the dermatologist evaluated the hydration of the skin with corneometry. The clinical examination consisted of physical examination of the breast skin, the corneometry measured numerically skin hydration. During treatment with radiotherapy, local side-effects were recorded according to the RTOG scale . Corneometer CM® 820 is a simple instrument that measure the water content of the skin. The examination is based on the measure of the ability of a dielectric medium, so any change in the dielectric constant caused by the change of hydration of the skin alters the measurement supplied by the condenser . The corneometry provides an indirect measure of the barrier function, and values of hydration of the skin are considered normal if included in the range 60–90 a.u.
Results were assessed not only in terms of grade and overall reduction in toxicity but also in terms of full regression of skin lesions with “ad integrum restitutio” and in terms of rapidity of repair of radio-induced damage assessed at 1 month after radiotherapy. At one month after the end of radiotherapy in all patients of groups A, B, C, E, it was recorded a G0 dermal toxicity. Eight patients in Group D had shown G1 toxicity. All patients completed the radiotherapy, and G4 cutaneous toxicity (according to RTOG scales (Table 3) was not observed in any patients .
The percentage of patients who underwent systemic therapies (chemotherapy, hormonal therapy and/or biological therapy) for each group are shown in Table 4. The complete results of the measurement with corneometry are shown in Table 5, that show the value of moisture of the skin measured with a corneometer. In general, corneometry values at starting point were between 40.5 (smallest median value) and 60.8 (highest median value) and at the end of treatment were between 45.7 (smallest median value) and 70.8 (highest median value). The low values of corneometry recorded at the beginning of treatment are certainly due to the alteration in skin of the breast treated surgically and any systemic treatments provided in specific cases.
We evaluated the correlation between the values measured with the corneometry in the various groups and systemic therapies carried out by the patients, in particular for each type of therapy (shown in Table 4) we evaluated the absolute risk reduction (ARR), relative risk (RR) and odds ratio (OR). We have not found a clear correlation between systemic treatments and the values of corneometry, probably for the small number of patients examined.
Regarding the correlation of the measurement with corneometry with the breast volumes, we found breast volumes > 500 cc both in groups B and D. We can hypothesize a correlation between breast volumes of the group D and skin toxicity, but without a statistical significance. The values of corneometry however were similar in these groups, so we can’t describe a direct correlation between the breast volumes, the corneometry values and the local toxicities.
Of the 20 patients, 18 showed G1 toxicity and 2 G2 toxicity during radiotherapy. All patients had a good grade of hydration measured with a corneometer, also at the first follow up. Betaglucan and sodium hyaluronate encourage and speed up the regeneration and quickens the healing of irradiated skin. The level of skin elasticity and skin dryness is good.
Of the 20 patients 16 showed G1 toxicity and 4 G2 toxicity during radiation therapy. Measurement of hydration showed a value of moisture of the skin with a slight decrease during the therapy and at the first follow up.
Of these patients 19 manifested G1 and 1 G2 toxicity at the conclusion of radiotherapy. The measurement with a corneometer emphasized the effective role of moisturizing cream. The Alga Atlantica has a central role in protection the skin’s microcapillary integrity.
Of 20 patients, 4 had G1 toxicity, 8 a G2 toxicity and 5 a G3 toxicity during the radiation treatment. Eight patients who suffered cutaneous toxicity during the treatment also showed G1 toxicity at the first follow up.
Of the 20 patients, 15 had a G1 cutaneous toxicity, 5 a G2 toxicity. Selectiose has a role in inflammatory reactions. Avene thermal water and glycin modulate itch and reddening.
The measurement with a corneometer confirmed the protective role of effective creams used in our Departmets routinely during radiation therapy of breast cancer. This allowed us to identify radiation induced dermatitis in a very early stage compared to only objective examination by allowing to treat early stage patients with a greater hydration or with steroid creams to intervene with early onset of erythema.
Skin side-effects, using radiotherapy techniques, are a common consequence of radical doses of radiotherapy, and many products have been introduced in order to prevent such side effects. Now radiation techniques have been improved but concomitantly there is a wider attention on the problems linked to skin irradiation. Currently, there is no standard approach for the prevention and treatment of radio-induced skin lesions, although several studies have been published on the use of various kinds of topical agents [14, 15]. Patients with breast cancer are increasing and their call for help expresses the need for new medical equipment. There is a growing attention on the local side effects of therapies in the field of oncology, and radiotherapy above all, also because there is an increasing request by these patients, to preserve as much as possible their physical aspect. Despite the common occurrence of radiation skin toxicity, there are very few trials on the argument.
In our study, we show that a good hydration of the skin before, during and after radiotherapy treatment can have a positive effect on the skin tolerance of treatment. In our clinical practice we use to prescribe moisturizers to all patients with an indication for radiotherapy for breast cancer. In fact we believe that a preventive therapy of the skin side effects is more effective than a treatment of the local side effects once they appear. This approach shows significant effectiveness in reducing the onset of acute dermal toxicity. Moreover, the radiotherapy treatments were well tolerated by patients and no treatment delays were necessary because of skin reactions. Acute radiodermatitis may affect the patients’ quality of life and daily activities. In some cases, unplanned gaps in treatment could occur, which decrease treatment efficacy . Apart from thorough skin cleaning and prevention of local irradiation-induced trauma, there is no well established protocol to prevent skin radiation toxicity . According to literature data we know that there are some risk factors including concurrent therapy, the use of bolus and smoking, previous or concomitant chemotherapy because of the change in the smallest blood vessels [4, 5].
In our experience we tested five different products in one hundred patients. The formulations of creams used showed good results. For all of them we received a satisfactory result, with only five patients with a grade 3 dermatitis and twenty with a grade 2 dermatitis. It is impossible for us to draw a conclusion about the question of what product is more active also because the number of patients is too small and because there are too many variables in the groups. In fact there are personal differencies, of the phototypes, but also differencies about the age of patients and the therapies that they received before, such as chemotherapy, or after surgery and concomitantly with radiotherapy, like ormonal therapy. The largest number of patients with a recorded skin toxicity a month after radiotherapy, in group D of our study, can be related to the patient’s biggest breast volumes, although we do not have a statistical significance. Moreover the values of corneometry allow us to attribute a good moisturizing effect for products used in five groups of patients. Certainly the creation of a multidisciplinary team has allowed, with the corneometry conducted at the same time of the clinical evaluation, to identify cases of skin toxicity in a first phase and to determine the appropriate treatment to prevent the onset of dermatitis of high level which may affect the tolerance of treatment for these women.
The first physiopathological step of radiation toxicity to the skin is known to be an overproduction of free radicals, which is responsible for damage to the basal epidermis layer cells and the endothelial cells. Degradation of the latter cells induces a perivascular inflammatory infiltrate around dilated blood vessels. Degradation of the former cells (proliferative layer) induces the transcription of pro-inflammatory cytokines, which are responsible for the inflammatory cascade. As a consequence of those effects, early radiodermatities are clinically observed [18–20]. The physiopathology of moist desquamation involves the loss of basal layer cells of epidermis. Erythema reflects an inflammatory response and a damage to basal layer cells. Aloe vera could be used to limit erythema, leading to an overall lower skin toxicity score. In literature, the prophylactic or therapeutic use of topical betamethasone is often present. The evaluation of skin side effects during and after a radiotherapy treatment normally is a clinical evaluation and it represents a subjective point of view of the phenomenon. In our study, we have combined clinical examination with corneometry. Although it is a measure of the water content of the skin, it is only an indirect measure of barrier function. However, there is a good relationship between numeric value and the extent of hydration under various physiological and pathological phenomena. Since water loss through the skin normally occurs by passive diffusion through the epidermis, smaller values indicate greater water loss and are consistent with increased damage of the barrier function of the stratum corneum [21–23]. Use of Corneometer to study water content of the skin is valid because of the skin has mechanic properties in relationship to hydration state; so a dry skin will be less elastic than moisturized skin. The assessment “in vivo” of the hydration is very important for clinical and experimental evaluation of the real capacity of a cream to moisturize skin and repair skin barrier. Some patients started radiotherapy already with low hydration value probably because of the chemotherapy treatment received before radiotherapy. Women treated for breast cancer request a satisfactory aesthetic condition according to a resolution of oncologic problems. It was impossible for us with a small number of patients, to evaluate which is the best product of the five used.
Our study confirms that moisturizers have an important value in the prevention of radiotherapy-induced skin damage and indicates that an instrumental assessment of skin hydration can help the radiation oncologist to use strategies that prevent the onset of toxicity of high degree.
Today it is ethically unacceptable to wait for the appearance of side effects to treat them. The prevention is required. Our patients receive a positive relationship with the radiation, which occurs after surgery and sometimes after chemotherapy, because they feel that the oncology team seeks to preserve their femininity. The interaction between medical specialties (Dermatology and Radiotherapy) has been valuable in this experience and has brought added value to the benefit of our patients.
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The authors declare that they have no competing interests.
ADL, MGC, SF, performed the literature search, extracted relevant articles and drafted the manuscript, VR, PM, PM, RM and SC contributed equally to this work participating in the design and coordination of the study, RDF, ES, FDN and FMG participated in the design of the study. All authors read and approved the final manuscript.