Brunner Patrick M, Jonak Constanze, Knobler Robert
Department of Dermatology, Medical University of Vienna, Währinger Gürtel 18-20, Vienna, 1090, Austria.
F1000Res. 2020 May 5;9. doi: 10.12688/f1000research.21922.1. eCollection 2020.
Cutaneous T-cell lymphomas (CTCLs) comprise a heterogeneous group of extranodal non-Hodgkin lymphomas involving primarily the skin and mycosis fungoides is its most frequent entity. Whereas most patients show an indolent course in early disease (clinical stages IA to IIA), some patients progress to advanced disease (stage IIB or higher), and the 5-year survival rate is unfavorable: only 47% (stage IIB) to 18% (stage IVB). Except for allogeneic stem cell transplantation, there is currently no cure for CTCL and thus treatment approaches are palliative, focusing on patients' health-related quality of life. Our aims were to review the current understanding of the pathogenesis of CTCL, such as the shift in overall immune skewing with progressive disease and the challenges of making a timely diagnosis in early-stage disease because of the lack of reliable positive markers for routine diagnostics, and to discuss established and potential treatment modalities such as immunotherapy and novel targeted therapeutics.
皮肤T细胞淋巴瘤(CTCL)是一组异质性的结外非霍奇金淋巴瘤,主要累及皮肤,蕈样肉芽肿是其最常见的类型。虽然大多数患者在疾病早期(临床IA至IIA期)表现为惰性病程,但一些患者会进展为晚期疾病(IIB期或更高分期),且5年生存率不佳:仅为47%(IIB期)至18%(IVB期)。除异基因干细胞移植外,目前CTCL尚无治愈方法,因此治疗方法是姑息性的,重点关注患者与健康相关的生活质量。我们的目的是回顾目前对CTCL发病机制的认识,例如随着疾病进展整体免疫偏向的转变,以及由于缺乏用于常规诊断的可靠阳性标志物而在疾病早期进行及时诊断所面临的挑战,并讨论已确立的和潜在的治疗方式,如免疫疗法和新型靶向治疗药物。