Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, State Key Laboratory of Complex Severe and Rare Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Beijing, China.
Department of Dermatology, People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, Yinchuan, China.
J Dermatolog Treat. 2024 Dec;35(1):2350231. doi: 10.1080/09546634.2024.2350231. Epub 2024 May 16.
Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma. This study was conducted to evaluate efficacy and safety of interferon (IFN) α-2a combined with phototherapy for early-stage MF. Thirteen patients with early-stage MF received subcutaneous injections of IFN α-2a at 3 million IU combined with phototherapy three times per week for 6 months. Treatment efficacy was measured by changes in body surface area (BSA) score and modified severity-weighted assessment tool (mSWAT) score at 1, 3, and 6 months after treatment. Histopathologic examinations of skin lesions were performed before and after treatment. After 3 months of treatment, all 13 patients achieved a partial response, and BSA and mSWAT scores were significantly lower than those at baseline ( < 0.001). After 6 months, BSA and mSWAT scores were significantly lower than those at baseline ( < 0.001) and after 3 months ( < 0.05). Eleven patients achieved complete remission and two patients achieved a partial response (overall response rate, 100%). Histopathologic examination showed a significant decrease in the number of atypical lymphocytes in both epidermis and dermis. No severe adverse effects occurred. IFN α-2a in combination with phototherapy may be an effective and safe alternative modality for early-stage MF.
蕈样肉芽肿(MF)是最常见的皮肤 T 细胞淋巴瘤。本研究旨在评估干扰素(IFN)α-2a 联合光疗治疗早期 MF 的疗效和安全性。13 例早期 MF 患者接受 IFN α-2a 皮下注射,剂量为 300 万 IU,联合光疗,每周 3 次,共 6 个月。治疗 1、3 和 6 个月后,通过体表面积(BSA)评分和改良严重程度加权评估工具(mSWAT)评分的变化来评估治疗效果。在治疗前后对皮肤病变进行组织病理学检查。治疗 3 个月后,所有 13 例患者均获得部分缓解,BSA 和 mSWAT 评分明显低于基线( < 0.001)。治疗 6 个月后,BSA 和 mSWAT 评分明显低于基线( < 0.001)和治疗 3 个月后( < 0.05)。11 例患者达到完全缓解,2 例患者达到部分缓解(总缓解率为 100%)。组织病理学检查显示表皮和真皮中异常淋巴细胞数量明显减少。未发生严重不良反应。IFN α-2a 联合光疗可能是早期 MF 的一种有效且安全的替代治疗方法。