医学
达拉图穆马
重症监护医学
硼替佐米
淋巴细胞白血病
急性淋巴细胞白血病
临床试验
肿瘤科
单克隆抗体
药品
化疗
白血病
生物信息学
Blinatumoab公司
梅德林
药品审批
多发性骨髓瘤
药物开发
来那度胺
作者
lorenzo celona,Eleonora Boscaro,Giulia Berutto,Davide Stella,Camilla Gariazzo,Federica Catania,Carlotta Zavatto,Chiara Dellacasa,Carolina Secreto,Elisa Santambrogio,Irene Urbino,Chiara Frairia,Valentina Giai,Stefano D’Ardìa,Roberto Freilone,Alessandro Busca,Ernesta Audisio,Marco Cerrano
标识
DOI:10.1080/17474086.2026.2678349
摘要
INTRODUCTION: The therapeutic landscape of acute lymphoblastic leukemia (ALL) in adults has greatly changed thanks to the introduction of response-adapted pediatric-inspired regimens and, in B-ALL, the advent of immunotherapy. More recently, the better understanding of genetics, the encouraging results of new agents and the evidence of activity of monoclonal antibodies and CAR-T cells are opening the road for meaningful advances in T-ALL. AREAS COVERED: We discuss the current therapeutic scenario of T-ALL in adults, including the basis of relevant chemotherapy backbones and a summary of recent biological advances with potential clinical implications. Besides, we summarize data of new drugs explored in the relapsed/refractory (R/R) setting and how they are moving frontline, including a focus of the emerging role of immunotherapy. EXPERT OPINION: The availability of effective agents like venetoclax, bortezomib and daratumumab may lead to improved frontline regimens, which will be tailored according to patient's genetics and drug response profile, and relevant role of CAR-T cell is foreseen, possibly beyond R/R setting. While several issues will require further studies, including central nervous system prophylaxis and treatment optimization in young adults and older patients, these advances will ultimately lead to improved efficacy, reduced toxicities and limited indications of allo-HCT.
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