Dermatology Department, Hospital Universitario Ramón y Cajal, Instituto de Investigación Sanitaria Ramón y Cajal (Irycis), 28034 Madrid, Spain.
Dermatology Department, Hospital 12 de Octubre, 28041 Madrid, Spain.
Int J Mol Sci. 2024 Feb 12;25(4):2203. doi: 10.3390/ijms25042203.
Mogamulizumab (MOG) is an antibody targeting the CCR4 receptor, authorized for relapsed or refractory peripheral T-cell (PTCL) and cutaneous T-cell lymphomas (CTCL). Its adoption in guidelines and endorsement by FDA and EMA established it as a systemic treatment, especially for advanced disease stages due to its comparatively lower toxicity. Clinical trials and real-world evidence have underscored its efficacy in advanced CTCLs, including mycosis fungoides and Sézary syndrome; PTCLs; and adult T-cell leukemia/lymphoma (ATLL), showcasing positive outcomes. Notably, the drug has demonstrated significant response rates, disease stability, and extended periods of progression-free survival, suggesting its applicability in cases with multiple treatment lines. Its safety profile is generally manageable, with adverse events (AEs) primarily related to the skin, infusion-related reactions, drug eruptions, autoimmune diseases, and skin disorders. The latter seem to appear as CCR4 can promote the skin-specific homing of lymphocytes, and MOG is directed against this receptor. While combination with immunostimulatory agents like interferon alpha and interleukin 12 has shown promising results, caution is urged when combining with PD1 inhibitors due to the heightened risk of immune-mediated AEs. The introduction of MOG as a systemic treatment implies a significant advancement in managing these diseases, supported by its favorable safety profile and complementary mechanisms.
莫格利珠单抗(mogamulizumab,MOG)是一种针对 CCR4 受体的抗体,被批准用于治疗复发或难治性外周 T 细胞淋巴瘤(PTCL)和皮肤 T 细胞淋巴瘤(CTCL)。其被纳入指南、获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)的认可,确立了其作为一种全身性治疗药物的地位,尤其适用于晚期疾病阶段,因为它的毒性相对较低。临床试验和真实世界证据强调了其在晚期 CTCL 中的疗效,包括蕈样真菌病和 Sezary 综合征、PTCL 以及成人 T 细胞白血病/淋巴瘤(adult T-cell leukemia/lymphoma,ATLL),展示了积极的结果。值得注意的是,该药物在多线治疗的情况下具有显著的反应率、疾病稳定性和较长的无进展生存期,表明其适用性。其安全性特征通常可管理,不良事件(adverse events,AEs)主要与皮肤相关,包括输注相关反应、药物皮疹、自身免疫性疾病和皮肤疾病。后者似乎是由于 CCR4 可以促进淋巴细胞的皮肤特异性归巢,而 MOG 则针对该受体。虽然与免疫刺激剂如干扰素-α和白细胞介素 12 联合使用显示出有前景的结果,但由于免疫介导的 AEs 风险增加,联合使用 PD1 抑制剂时需要谨慎。MOG 作为一种全身性治疗药物的引入,支持其有利的安全性特征和互补机制,代表了这些疾病管理的重大进展。