Mehta-Shah Neha, Ratner Lee, Horwitz Steven M
Washington University, St Louis, MO; and Memorial Sloan Kettering Cancer Center, New York, NY.
J Oncol Pract. 2017 Aug;13(8):487-492. doi: 10.1200/JOP.2017.021907.
Adult T-cell lymphoma/leukemia (ATL) is a rare T-cell lymphoproliferative neoplasm caused by human T-lymphotrophic virus 1. In its more common, aggressive forms, ATL carries one of the poorest prognoses of the non-Hodgkin lymphomas. The disease has clinical subtypes (ie, acute, lymphoma, chronic, and smoldering forms) defined by the presenting features, and therefore, the clinical course can vary. For the smoldering and lower-risk chronic forms, combinations involving antiviral therapies have shown some success. However, in many patients, the more indolent forms will evolve into the more aggressive subtypes. In the more aggressive acute, lymphoma, and higher-risk chronic forms, the literature supports initial treatment with combination chemotherapy followed by allogeneic transplantation as a potentially curative approach. Recently, mogamulizumab and lenalidomide have shown promise in the treatment of ATL. With better understanding of the molecular drivers of this disease, we hope that the therapeutic landscape will continue to expand.
成人T细胞淋巴瘤/白血病(ATL)是一种由人类T淋巴细胞病毒1引起的罕见的T细胞淋巴增殖性肿瘤。在其更常见、侵袭性更强的形式中,ATL的预后是所有非霍奇金淋巴瘤中最差的之一。该疾病有根据临床表现定义的临床亚型(即急性、淋巴瘤、慢性和潜伏形式),因此,临床病程可能有所不同。对于潜伏性和低风险慢性形式,涉及抗病毒治疗的联合治疗已取得了一些成效。然而,在许多患者中,较惰性的形式会演变为更具侵袭性的亚型。在更具侵袭性的急性、淋巴瘤和高风险慢性形式中,文献支持以联合化疗作为初始治疗,随后进行异基因移植,这是一种可能治愈的方法。最近,莫加莫单抗和来那度胺在ATL治疗中显示出了前景。随着对该疾病分子驱动因素的进一步了解,我们希望治疗方法的范围将继续扩大。