Rozati Sima, Kim Youn H
Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Curr Opin Oncol. 2016 Mar;28(2):166-71. doi: 10.1097/CCO.0000000000000272.
Cutaneous T-cell lymphoma (CTCL) comprises a heterogeneous group of malignancies derived from skin-homing or resident T cells. Effective treatments are limited, thus new therapies are in development to address the unmet medical need.
Recent studies uncovering the genetic alteration in cutaneous T-cell lymphoma have enhanced our understanding of the importance of the T-cell activation/survival pathways, dysregulated immune system, and the relevance of chromatin modification in the pathogenesis of CTCL. New advances in cancer immunomodulation such as with PD1/PD-L1 inhibitors and novel targeted antitumor therapies such as brentuximab vedotin and mogamulizumab as well as potential combination strategies are promising for improving clinical efficacy with manageable toxicity profile.
All these new therapeutic approaches have resulted in broadening the treatment landscape and a potential paradigm shift in the management of CTCL.
皮肤T细胞淋巴瘤(CTCL)是一组异质性恶性肿瘤,起源于归巢至皮肤或驻留在皮肤的T细胞。有效的治疗方法有限,因此正在研发新的疗法以满足未被满足的医疗需求。
最近关于皮肤T细胞淋巴瘤基因改变的研究增进了我们对T细胞激活/存活途径、免疫系统失调以及染色质修饰在CTCL发病机制中的相关性的重要性的理解。癌症免疫调节方面的新进展,如使用PD1/PD-L1抑制剂,以及新型靶向抗肿瘤疗法,如brentuximab vedotin和mogamulizumab,以及潜在的联合策略,有望在毒性可控的情况下提高临床疗效。
所有这些新的治疗方法拓宽了CTCL的治疗前景,并可能在其管理方面引发范式转变。