Early T-cell precursors (ETP) are the earliest progenitors that originate from the bone marrow and reside in the thymus. Early T-cell precursor acute lymphoblastic leukemia (ETP-ALL) is a new subtype of T-cell acute lymphoblastic leukemia (T-ALL) that is discovered with the advancement of research techniques. The traditional view of hematopoiesis is that hematopoietic cells follow a basic process of lineage commitment from multipotent stem cells to lineage-restricted progenitor cells. The first step of hematopoiesis is common myeloid and lymphoid differentiation pathways,and the final step of T lymphocyte lineage restriction occurs in the thymus. However,ETP-ALL has differential potential of T,B and myeloid cells,challenging the traditional hematopoietic lineage development rules. At present,the lineage origin and differential potential of ETP-ALL can not be clearly identified,so its immune phenotype,genetic characteristics and diagnosis and treatment are being investigated,which also increases the difficulty of diagnosis and differential diagnosis. Currently,the flow cytometry immuno-phenotyping scoring system is an important auxiliary diagnostic method of ETP-ALL. ETP-ALL treatment typically includes induction therapy,consolidation therapy after remission and maintenance therapy. Due to poor response to conventional chemotherapy and high relapse rate after remission,patients who achieve complete remission and meet the criteria should perform allogeneic hematopoietic stem cell transplantation as soon as possible. This review provides an overview of the origin and regulation of ETP-ALL,as well as the latest advances in the laboratory diagnosis and clinical treatment of ETP-ALL,which may be useful for its diagnosis and treatment.