Anna V. Michenko, Larisa S. Kruglova, Evgeniya A. Shatokhina, Andrey N. Lvov, Ekaterina M. Simenskaya, Dmitry V. Romanov, Inessa B. Kononenko, Anton V. Snegovoy
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 This article presents a case of uremic pruritus in a patient with papulo-pustular cutaneous reaction (grade II on a Scale Common Terminology Criteria for Adverse Events, CTCAE v 5.0) to the epidermal growth factor (EGFR) inhibitor cetuximab in combination with leucovorin and 5-fluorouracil for rectal cancer. Treatment of uremic pruritus with small doses of gebapentin (300 mg/day) led to complete regression of pruritus. Papulo-pustular rashes completely regressed after recommended systemic and topical therapy according to the severity of rush (doxycycline 100 mg 2 times a day for 5 days, cream with neomycin, natamycin and hydrocortisone 3 times a day for 7 days). Pruritus was absent during the next 6 months of follow-up. Antitumor therapy was not interrupted due to acneiform rush, and following supportive topical therapy allowed to control severity of exacerbations which did not exceed III grade according to CTCAE v 5.0 and did not require the addition of systemic therapy.
 Thus, therapy of uremic pruritus with gabapentin has shown was effective also in a patient with severe comorbid pathology. Supportive topical therapy consistent with the severity of papulo-pustular rash reduced the severity of exacerbations during following EGFR inhibitor therapy.","PeriodicalId":487039,"journal":{"name":"Rossiiskii Zhurnal Kozhnykh i Venericheskikh Boleznei","volume":"53 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A case of uremic pruritus and papulo-pustular rash associated with anti-EGFR therapy in a patient with rectal cancer and chronic kidney disease\",\"authors\":\"Anna V. Michenko, Larisa S. Kruglova, Evgeniya A. Shatokhina, Andrey N. Lvov, Ekaterina M. Simenskaya, Dmitry V. Romanov, Inessa B. Kononenko, Anton V. Snegovoy\",\"doi\":\"10.17816/dv340919\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Uremic pruritus is a common symptom in chronic kidney disease and end-stage renal failure. In addition to physical discomfort uremic pruritus disrupts sleep, negatively affects the psycho-emotional state and quality of life. In this group of patients, the association of uremic pruritus with an increase in mortality due to any causes was demonstrated. At the same time, there are no standardized approaches to the treatment of uremic itching. There is also a special category of patients receiving antitumor therapy and developing dermatological adverse events, also potentially accompanied by itching.
 This article presents a case of uremic pruritus in a patient with papulo-pustular cutaneous reaction (grade II on a Scale Common Terminology Criteria for Adverse Events, CTCAE v 5.0) to the epidermal growth factor (EGFR) inhibitor cetuximab in combination with leucovorin and 5-fluorouracil for rectal cancer. Treatment of uremic pruritus with small doses of gebapentin (300 mg/day) led to complete regression of pruritus. Papulo-pustular rashes completely regressed after recommended systemic and topical therapy according to the severity of rush (doxycycline 100 mg 2 times a day for 5 days, cream with neomycin, natamycin and hydrocortisone 3 times a day for 7 days). Pruritus was absent during the next 6 months of follow-up. Antitumor therapy was not interrupted due to acneiform rush, and following supportive topical therapy allowed to control severity of exacerbations which did not exceed III grade according to CTCAE v 5.0 and did not require the addition of systemic therapy.
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引用次数: 0
摘要
尿毒症瘙痒是慢性肾脏疾病和终末期肾功能衰竭的常见症状。除身体不适外,尿毒症瘙痒会扰乱睡眠,对心理情绪状态和生活质量产生负面影响。在这组患者中,尿毒症瘙痒与任何原因引起的死亡率增加的关联得到了证实。同时,治疗尿毒症瘙痒没有标准化的方法。还有一类特殊的患者接受抗肿瘤治疗并出现皮肤不良事件,也可能伴有瘙痒。
本文报道一例尿毒症性瘙痒,患者对表皮生长因子(EGFR)抑制剂西妥昔单抗联合亚叶酸钙和5-氟尿嘧啶治疗直肠癌有丘疹-脓疱性皮肤反应(二级不良事件通用术语标准,CTCAE v 5.0)。小剂量(300mg /天)治疗尿毒症性瘙痒可使瘙痒完全消退。根据皮疹的严重程度,推荐全身和局部治疗丘疹-脓疱性皮疹后完全消退(强力霉素100 mg每天2次,持续5天,新霉素、纳他霉素和氢化可的松乳膏每天3次,持续7天)。在接下来的6个月的随访中没有瘙痒。抗肿瘤治疗没有因痤疮发作而中断,并且根据CTCAE v 5.0,支持局部治疗可以控制恶化的严重程度,不超过III级,不需要增加全身治疗。
因此,加巴喷丁治疗尿毒症性瘙痒对有严重合并症的患者也有效。支持局部治疗与丘疹-脓疱疹的严重程度一致,降低了EGFR抑制剂治疗后恶化的严重程度。
A case of uremic pruritus and papulo-pustular rash associated with anti-EGFR therapy in a patient with rectal cancer and chronic kidney disease
Uremic pruritus is a common symptom in chronic kidney disease and end-stage renal failure. In addition to physical discomfort uremic pruritus disrupts sleep, negatively affects the psycho-emotional state and quality of life. In this group of patients, the association of uremic pruritus with an increase in mortality due to any causes was demonstrated. At the same time, there are no standardized approaches to the treatment of uremic itching. There is also a special category of patients receiving antitumor therapy and developing dermatological adverse events, also potentially accompanied by itching.
This article presents a case of uremic pruritus in a patient with papulo-pustular cutaneous reaction (grade II on a Scale Common Terminology Criteria for Adverse Events, CTCAE v 5.0) to the epidermal growth factor (EGFR) inhibitor cetuximab in combination with leucovorin and 5-fluorouracil for rectal cancer. Treatment of uremic pruritus with small doses of gebapentin (300 mg/day) led to complete regression of pruritus. Papulo-pustular rashes completely regressed after recommended systemic and topical therapy according to the severity of rush (doxycycline 100 mg 2 times a day for 5 days, cream with neomycin, natamycin and hydrocortisone 3 times a day for 7 days). Pruritus was absent during the next 6 months of follow-up. Antitumor therapy was not interrupted due to acneiform rush, and following supportive topical therapy allowed to control severity of exacerbations which did not exceed III grade according to CTCAE v 5.0 and did not require the addition of systemic therapy.
Thus, therapy of uremic pruritus with gabapentin has shown was effective also in a patient with severe comorbid pathology. Supportive topical therapy consistent with the severity of papulo-pustular rash reduced the severity of exacerbations during following EGFR inhibitor therapy.