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Research Advances of Genetics, Diagnosis and Treatment of T-cell Prolymphocytic Leukemia--Review / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1977-1981, 2021.
Article in Zh | WPRIM | ID: wpr-922235
Responsible library: WPRO
ABSTRACT
T-cell prolymphocytic leukemia (T-PLL) is a rare but highly aggressive and malignant mature T-lymphoid tumor. The diagnosis of T-PLL mainly depend on genetic characteristics, clinical manifestations, cell morphology and immunophenotype. At present, clinical treatment is mainly aimed at improving the response rate and prolonging the remission period. With the development of new molecular biology technologies, researchers have gained a deeper understanding of the pathogenesis and related genetics of T-PLL, targeted drugs, including HDAC inhibitors, JAK/STAT inhibitors, AKT inhibitors and BCL-2 inhibitors, are also under evolution and providing the new opportunities to improve the efficacy of therapy. In this review, the advances in genetics and treatment of T-PLL were summarized briefly.
Subject(s)
Full text: 1 Database: WPRIM Main subject: Leukemia, Prolymphocytic, T-Cell / Immunophenotyping / Protein Kinase Inhibitors / Antineoplastic Agents Type of study: Diagnostic_studies Limits: Humans Language: Zh Journal: Journal of Experimental Hematology Year: 2021 Document type: Article
Full text: 1 Database: WPRIM Main subject: Leukemia, Prolymphocytic, T-Cell / Immunophenotyping / Protein Kinase Inhibitors / Antineoplastic Agents Type of study: Diagnostic_studies Limits: Humans Language: Zh Journal: Journal of Experimental Hematology Year: 2021 Document type: Article