IRCCS - Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Istituto di Ematologia "Seràgnoli", Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università Degli Studi, Bologna, Italy.
Acta Haematol. 2022;145(2):207-209. doi: 10.1159/000518815. Epub 2021 Oct 13.
Mycosis fungoides (MF) is a disease almost impossible to cure. In the context of heavily pretreated patients, the anti-programmed cell death protein 1 (anti-PD-1) pembrolizumab is a valid therapeutic option. The alteration of the PD-1-PD ligand 1 (PD-L1) axis is often present in MF, and this aspect explains the feasibility of this therapy. We report the case of a 60-year-old woman diagnosed with MF in 2003, Olsen stage IA (T1M0NXBO). Since the moment of the diagnosis, she received 10 lines of therapy, with a short duration of response after each one of them. In April 2020, our patient started pembrolizumab 2 mg/kg every 3 weeks, and she achieved a partial response after the 4th cycle, consistent with the modified severity assessment tool (mSWAT) 1, which she is still maintaining after 10 cycles. No grade ≥3 adverse events were recorded. We conclude that pembrolizumab can induce extremely rapid responses in MF, with very low toxicity.
蕈样肉芽肿(MF)是一种几乎无法治愈的疾病。在经过大量预处理的患者中,抗程序性细胞死亡蛋白 1(抗 PD-1)的派姆单抗是一种有效的治疗选择。PD-1-PD 配体 1(PD-L1)轴的改变在 MF 中经常存在,这一特点解释了这种治疗的可行性。我们报告了一例 60 岁女性患者,2003 年诊断为 MF,Olsen 分期为 IA(T1M0NXBO)。自诊断以来,她接受了 10 种治疗方案,但每种方案的反应持续时间都很短。2020 年 4 月,我们的患者开始接受派姆单抗 2 mg/kg,每 3 周一次,在第 4 个周期后达到部分缓解,符合改良严重程度评估工具(mSWAT)1,在 10 个周期后仍在维持。没有记录到≥3 级的不良事件。我们得出结论,派姆单抗可以在 MF 中诱导极其迅速的反应,且毒性非常低。