• 한방안이비인후피부과학회지
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• 제35권4호
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• pp.181-189
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• 2022

Objectives : The purpose of this study is to report a case of Korean medicine on acute radiation dermatitis. Methods : This study was conducted with an acute radiation dermatitis patient who hospitalized in ophthalmology, otolaryngology & dermatology clinic of Korean medical hospital. The patient was treated with Korean medicine including acupuncture, wet dressing, herbal ointment and phototherapy. We evaluated the patient's subject symptoms before and after treatment using the VAS scale and CTCAE. Results : The patient's subjective symptoms were improved after treatment. Conclusions : It is considered that Korean medicine could be applied to the treatment of acute radiation dermatitis.

• Radiation Oncology Journal
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• 제35권3호
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• pp.289-294
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• 2017

Sorafenib is widely used for unresectable and metastatic hepatocellular carcinomas. Radiation recall dermatitis (RRD) is an acute inflammatory reaction confined to previously irradiated skin that occurs after the administration of certain drugs. RRD after sorafenib treatment is rare; five cases have been reported thus far. We describe a 44-year-old man irradiated for chest wall bone metastasis from hepatocellular carcinoma. Eight days after radiotherapy completion, systemic therapy for metastatic hepatocellular carcinoma was initiated with sorafenib treatment. Eleven days after starting sorafenib, the patient complained of erythematous rash with pruritus in the chest wall, in a location consistent with the previous radiation field. Sorafenib was continued at the same dose, despite the RRD. The skin reaction subsided over the next 2 weeks without any medical intervention.

• Asian Pacific Journal of Cancer Prevention
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• 제14권8호
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• pp.4859-4864
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• 2013

Background: The purpose of this study was to assess the effectiveness of a recombinant human epidermal growth factor (EGF)-based cream for the prevention of acute radiation dermatitis in breast cancer patients receiving radiotherapy (RT). Materials and Methods: Between December 2012 and April 2013, 40 breast cancer patients who received postoperative RT were prospectively enrolled in this study and randomly assigned to receive human recombinant EGF-based cream (intervention group) or general supportive skin care (control group). The grade of radiation dermatitis and pain score were examined at weekly intervals during RT and 6 weeks after RT completion. Results: All patients completed the planned RT and complied well with instructions for applying the study cream and general supportive skin care. In the intervention group, radiation dermatitis of maximum grade 3, 2, and 1 developed in 3 (15%), 11 (55%), and 6 patients (30%), respectively. In comparison, in the control group, radiation dermatitis of maximum grade 3, 2, and 1 developed in 8 (40%), 10 (50%), and 2 patients (10%), respectively. The intervention group showed lower incidence of grade 3 radiation dermatitis than the control group (p=0.068 in univariate analysis and p=0.035 in multivariate analysis). There was no statistically significant difference in the maximal pain score between the two groups (p=0.934). Conclusions: This single-blind randomized preliminary study showed that recombinant human EGF-based cream can have a beneficial role in preventing or minimizing radiation dermatitis in breast cancer patients. To confirm the results of our study, additional studies with a large sample size are required.

• Radiation Oncology Journal
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• 제32권3호
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• pp.156-162
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• 2014

Purpose: This study was designed to evaluate the efficacy and safety of topically applied recombinant human epidermal growth factor (rhEGF) for the prevention of radiation-induced dermatitis in cancer patients. Materials and Methods: From December 2010 to April 2012, a total of 1,172 cancer patients who received radiotherapy (RT) of more than 50 Gy were prospectively enrolled and treated with EGF-based cream. An acute skin reaction classified according to the Radiation Therapy Oncology Group 6-point rating scale was the primary end point and we also assessed the occurrence of edema, dry skin, or pruritus. Results: The percentage of radiation dermatitis with maximum grade 0 and grade 1 was 19% and 58% at the time of 50 Gy, and it became 29% and 47% after completion of planned RT. This increment was observed only in breast cancer patients (from 18%/62% to 32%/49%). Adverse events related to the EGF-based cream developed in 49 patients (4%) with mild erythema the most common. Skin toxicity grade >2 was observed in 5% of the patients. Edema, dry skin, and pruritus grade ${\geq}3$ developed in 9%, 9%, and 1% of the patients, respectively. Conclusion: Prophylactic use of an EGF-based cream is effective in preventing radiation dermatitis with tolerable toxicity. Further studies comparing EGF cream with other topical agents may be necessary.

• Radiation Oncology Journal
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• 제29권4호
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• pp.236-242
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• 2011

Purpose: To compare photon thunderbird with deep match (technique 1) with 3-field technique with electron inguinal boost (technique 2) in acute skin toxicity, toxicity-related treatment breaks and patterns of failure in elective inguinal radiation therapy (RT) for curative chemoradiation in anal cancer. Materials and Methods: Seventeen patients treated between January 2008 and September 2010 without evidence of inguinal and distant metastasis were retrospectively reviewed. In 9 patients with technique 1, dose to inguinal and whole pelvis area was 41.4 to 45 Gy and total dose was 59.4 Gy. In 8 patients with technique 2, doses to inguinal, whole pelvis, gross tumor were 36 to 41.4 Gy, 36 to 41.4 Gy, and 45 to 54 Gy, respectively. The median follow-up period was 27.6 and 14.8 months in group technique 1 and 2, respectively. Results: The incidences of grade 3 radiation dermatitis were 56% (5 patients) and 50% (4 patients), dose ranges grade 3 dermatitis appeared were 41.4 to 50.4 Gy and 45 to 54 Gy in group technique 1 and 2, respectively (p = 0.819). The areas affected by grade 3 dermatitis in 2 groups were as follow: perianal and perineal areas in 40% and 25%, perianal and inguinal areas in 0% and 50%, and perianal area only in 60% and 25%, respectively (p = 0.196). No inguinal failure has been observed. Conclusion: Photon thunderbird with deep match technique and 3-field technique with electron inguinal boost showed similar incidence of radiation dermatitis. However, photon thunderbird with deep match seems to increase the possibility of severe perineal dermatitis.

• 한국방사선학회논문지
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• 제17권2호
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• pp.231-242
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• 2023

본 연구는 방사선치료를 받은 환자의 방서선 피부염에 대한 관리실태와 만족도를 조사하여 방사선 피부염의 발생을 줄이고 환자의 만족도를 향상시키기 위한 기초자료로 제공하고자 한다. 2022년 10월 28일 부터 2023년 4월 4일까지 부산 소재 G 병원을 내원하여 방사선치료 받은 유방암 환자 137명에게 설문조사를 시행하였다. 피부 반응 측정의 기준으로는 Radiation Therapy Oncolcgy Group(RTOG) cutaneous acute radiothe rapy toxicity score를 이용하였으며, 암병기 수준과 RTOG 연관성을 분석하였다. 통계분석에는 SPSS 프로그램(ver,18.0)을 이용하였다. 방사선 피부염 발생 빈도는 RTOG 0~1이 73% 였고, 2~3이 27%로 비교적 낮았다. RTOG 그룹별 방사선치료 후 만족도는 통계적으로 유의하게 나타났으며, 피부염 정도가 낮을수록 만족하였고, 피부염 정도가 심할수록 불만족 하였다.(p=0.001) 알로에 베라 미스트 사용 빈도에 따른 RTOG그룹과 피부 만족도는 유의수준 5%에서 통계적 차이를 보이지 않았으나(p=0.065), 하루에 1~2회 사용하는 그룹(69.3%)에서는 만족도가 높은 경향을 보였다. 알로에 베라 미스트 사용 시 체감 효과는 RTOG가 높은 그룹일수록 열감 감소 효과(p=0.001), 통증 감소 효과(p=0.033), 가려움 감소 효과(p=0.001), 심리적 안정 효과(p=0.027)가 통계적으로 유의하게 나타났다. 또한 암 병기 수준이 올라갈수록 방사선 피부염 정도도 심해지고 있으며 이는 통계적으로 유의하였다(p=0.001). 결론적으로 방사선 피부염은 방사선치료 시 가장 흔한 부작용으로, 환자 개인의 피부 민감도 및 치료 외부 인자 등에 의해 다양하게 나타난다. 치료 전 충분한 교육과 MD Cream, 알로에 베라 미스트 사용을 권장함으로써 방사선 피부염 발생률을 낮추고 예방 및 관리가 필요하다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권11호
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• pp.4483-4486
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• 2014

Purpose: To assess chemoradiation related acute morbidity in women with carcinoma cervix and to find and correlation between hematologic toxicity and organ system specific damage. Materials and Methods: A prospective study was carried out between August 2012 and July 2013 enrolling 79 women with cancer cervix receiving chemo-radiotherapy. Weekly assessment of acute morbidity was done using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4 and the toxicities were graded. Results: Anemia [77 (97.5%)], vomiting [75 (94.8%)] and diarrhea [72 (91.1%)], leukopenia [11 (13.9%)], cystitis [28 (35.4%], dermatitis [19 (24.1%)] and fatigue [29 (36.71%)] were the acute toxicities noted. The toxicities were most severe in $3^{rd}$ and $5^{th}$ week. All women could complete radiotherapy except two due to causes unrelated to radiation morbidity; seven (8.86%) had to discontinue chemotherapy due to leukopenia and intractable diarrhea. Though there was no correlation between anemia and other toxicities, it was found that all with leukopenia had diarrhea. Conclusions: Chemoradiation for cancer cervix is on the whole well tolerated. Leukopenia and severe diarrhea were the acute toxicities that compelled discontinuation of chemotherapy in two women. Though anemia had no correlation with gastrointestinal toxicity, all of those with leukopenia had diarrhea.

• Radiation Oncology Journal
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• 제26권4호
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• pp.222-228
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• 2008

목 적: 항문암의 방사선치료는 급성부작용을 많이 동반하므로 다양한 치료 기법이 적용되어왔다. 본원에서 시행된 항문암 방사선치료를 회음부 피부반응의 측면에서 검토하여 최적의 방사선치료 기법을 모색하고자 하였다. 대상 및 방법: 1990년부터 2007년까지 항문암으로 근치적 항암화학방사선치료를 마친 환자 35명을 대상으로 방사선 조사 방법 및 관련된 임상적 자료들을 이용하였다. 방사선치료는 원발병소, 영역림프절 및 서혜부림프절이 치료범위에 포함된 상태로 1.8 Gy 씩 $41.4{\sim}45\;Gy$ 조사 후 원발 병소 또는 전이성 림프절에 추가 조사하는 것을 원칙으로 하였다. 방사선 조사 기법은 조사 부위 및 조사 수에 따라 4가지로 분류하였으며 각 기법에 따른 회음부 급성피부반응 및 치료중지기간 간의 관련 여부를 알아보았다. 결 과: 방사선치료 중 28명(80.0%)의 환자에서 2등급 이상의 방사선 피부염이 발생하였고 10명(28.5%)이 3등급 이상의 방사선 피부염을 보였다. 4가지 방사선 조사 기법 중 원발병소와 영역림프절에 대한 3면 X-선 및 양측 서혜부림프절에 대한 전자선 조사 군과 electron thunderbird군에서 방사선 피부염이 동반된 환자 수가 상대적으로 적었으며 치료중지기간이 각각 $8.2{\pm}10.2$일, $5.7{\pm}5.7$일로써 다른 치료 기법보다 적었다. 방사선치료 종료 후 1개월 시점에서 27명(77.1%)의 환자에서 완전 관해를 보였으며 5년 생존율은 67.7%이었다. 결 론: 항문암의 방사선치료에 있어 방사선 조사 방법 및 범위가 치료순응도에 영향을 미칠 수 있으며, X-선의 회음부 조사 범위를 줄이는 방법이 회음부의 심각한 방사선 피부염을 감소시킴으로써 환자의 치료순응도를 높이는 데 있어 적절할 것으로 생각된다.

• Asian Pacific Journal of Cancer Prevention
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• 제16권16호
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• pp.7331-7335
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• 2015

Background: Concurrent chemoradiation with three weekly high dose cisplatin is the non-surgical standard of care for the treatment of locally advanced head and neck cancers. Although this treatment regime is efficacious, it has high acute toxicity, which leads not only to increased treatment cost, but also to increased overall treatment time. Hence, the current study was undertaken to evaluate the acute toxicity and tumor response in head and neck cancer patients treated with concurrent chemoradiation using $40mg/m^2$ weekly cisplatin, which has been our institutional practice. Materials and Methods: This single institution retrospective study included data for 287 head and neck cancer patients treated with concurrent chemoradiation from 2012 to 2014. Results: The mean age of the patients was 48.8 years. The most common site of involvement was oral cavity. Most of the study patients presented with advanced stage disease. The mean overall treatment time was 56.9 days. Some 67.2% had overall complete response to treatment as documented till 90 days from the start of treatment. According to the Radiation Therapy Oncology Group (RTOG) acute radiation morbidity scoring criteria, mucositis was seen in 95.1% of the patients. Dermatitis and emesis were observed in 81.9% and 98.6%, respectively. Regarding haematological toxicity, 48.8% and 29.6% suffered from anaemia and leukopenia, respectively, during treatment. Acute kidney injury was assessed using the Common Terminology Criteria for Adverse Events (CTCAE), and was found in 18.8% of the patients. Conclusions: Concurrent chemoradiotherapy with weekly cisplatin is an effective treatment regime for head and neck cancers with reasonable toxicity which can be used in developing countries, where cost of treatment is so important.

• Asian Pacific Journal of Cancer Prevention
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• 제14권9호
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• pp.5175-5178
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• 2013

Background: The prognostic value of tumor osteopontin (OPN) in patients with squamous-cell head and neck cancer (SCHNC) was investigated. Materials and Methods: OPN expression was assessed by immunohistochemical methods in 50 patients, who were treated with primary radiotherapy (RT) for locally advanced SCHNC. The effects of OPN on clinical parameters, local-regional control after RT and metastasis-free survival, was assessed. Results: The rate of OPN expression in tumor tissue was 76%. OPN positive cases had lower Hb levels (p=0.088). Mean time to local recurrence was 53.8 months (SE 3.9) in OPN-negative cases and 39.1 months (SE 4.7) in OPN-positive cases (p=0.047). OPN increased the risk of local recurrence 5.9 times (p=0.085). It had no effect on metastasis-free (p=0.116) or overall survival (p=0.123). OPN was positive in 12 of 19 cases that developed grade 3-4 acute radiation dermatitis (p=0.096). Conclusions: OPN expression is associated with an increase in local recurrence in patients who were treated with primary RT for locally advanced SCHNC.