Department of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, China.
Department of Pharmacy, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.
J Clin Pharm Ther. 2022 Feb;47(2):194-199. doi: 10.1111/jcpt.13542. Epub 2021 Oct 15.
Knowledge regarding the association between photosensitivity and pirfenidone is based mainly on case reports. The purpose of this article was to evaluate the clinical characteristics of photosensitivity associated with pirfenidone.
We collected studies on photosensitivity induced by pirfenidone published from 2008 to 31 August 2021 in Chinese and English for a retrospective analysis.
The median age was 70 years (range 57-80) in 22 patients with pirfenidone-induced photosensitivity. The dose at the onset of symptoms ranged from 600 to 2403 mg for the treatment of idiopathic pulmonary fibrosis. Pirfenidone-induced photosensitivity occurred within 1 week in some patients and up to 8 months in others. The most common clinical manifestation of photosensitivity caused by pirfenidone was itching on body parts exposed to sunlight (back of hands, face, neck, and limbs) in 15 patients followed by erythema in 13 patients. Histopathological examination revealed necrotic keratinocytes, lymphocytic inflammatory cell infiltrate, hyperkeratosis and liquefaction degeneration in 5 patients. The photosensitivity test showed a markedly decreased minimum erythema dose (MED) of 7-228 mJ/cm UV-B in 4 patients and 4.86-12 J/cm UV-A in 5 patients. The clinical symptoms were significantly improved or completely relieved with a median time of 4 weeks (range 1-8) after drug withdrawal, dose reduction or systemic and topical glucocorticoid therapy.
Clinicians should be aware of the potential phototoxic effects of pirfenidone and should inform patients to take pirfenidone during (or after) a meal, avoid sun exposure, wear protective clothing, and apply broad-spectrum sunscreen with high ultraviolet UVA and UVB protection.
关于光敏性与吡非尼酮之间关联的知识主要基于病例报告。本文的目的是评估与吡非尼酮相关的光敏性的临床特征。
我们收集了 2008 年至 2021 年 8 月 31 日期间以中文和英文发表的关于吡非尼酮诱导的光敏性的研究,进行回顾性分析。
22 例吡非尼酮诱导的光敏性患者的中位年龄为 70 岁(范围 57-80 岁)。症状发作时的剂量范围为 600-2403mg 用于治疗特发性肺纤维化。在一些患者中,吡非尼酮诱导的光敏性发生在 1 周内,而在其他患者中则长达 8 个月。15 例患者出现吡非尼酮引起的光敏性的最常见临床表现是暴露于阳光的身体部位(手背、面部、颈部和四肢)瘙痒,其次是 13 例患者出现红斑。5 例患者的组织病理学检查显示坏死角质形成细胞、淋巴细胞炎性细胞浸润、过度角化和液化变性。4 例患者的光敏试验显示最小红斑剂量(MED)明显下降,UV-B 为 7-228mJ/cm,5 例患者的 UV-A 为 4.86-12J/cm。停药、减少剂量或全身和局部糖皮质激素治疗后,中位时间为 4 周(范围 1-8 周),临床症状显著改善或完全缓解。
临床医生应意识到吡非尼酮存在潜在的光毒性作用,应告知患者在(或之后)用餐期间服用吡非尼酮,避免阳光照射,穿着防护服,并涂抹具有高紫外线 UVA 和 UVB 保护的广谱防晒霜。