医学
单克隆抗体
嵌合抗原受体
疾病
临床试验
皮肤T细胞淋巴瘤
淋巴瘤
造血干细胞移植
化疗
肿瘤科
免疫学
皮肤病科
皮肤淋巴瘤
癌症研究
病理
蕈样真菌病
作者
Reinhard Dummer,Maarten H. Vermeer,J. Scarisbrick,Youn H. Kim,Connor J. Stonesifer,Cornelis P. Tensen,Larisa J. Geskin,Pietro Quaglino,Egle Ramelyte
标识
DOI:10.1038/s41572-021-00296-9
摘要
Primary cutaneous T cell lymphomas (CTCLs) are a heterogeneous group of lymphomas that present in the skin with no evidence of extracutaneous disease at the time of diagnosis. CTCL subtypes demonstrate a variety of clinical, histological, and molecular features, and can follow an indolent or a very aggressive course. The underlying pathogenetic mechanisms are not yet entirely understood. The pathophysiology of CTCL is complex and a single initiating factor has not yet been identified. Diagnosis is based on clinicopathological correlation and requires an interdisciplinary team. Treatment decision is made based on short-term and long-term goals. Therapy options comprise skin-directed therapies, such as topical steroids or phototherapy, and systemic therapies, such as monoclonal antibodies or chemotherapy. So far, the only curative treatment approach is allogeneic haematopoietic stem cell transplantation. Novel therapies, such as chimeric antigen receptor T cells, monoclonal antibodies or small molecules, are being investigated in clinical trials. Patients with CTCL have reduced quality of life and a lack of effective treatment options. Further research is needed to better identify the underlying mechanisms of CTCL development and course as well as to better tailor treatment strategies to individual patients.
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