达拉图穆马
CD38
单克隆抗体
多发性骨髓瘤
抗体
癌症研究
医学
免疫学
生物
遗传学
干细胞
川地34
作者
Emiliano Barbieri,Enrica Antonia Martino,Elena Rivolti,Micol Quaresima,Ernesto Vigna,Antonino Neri,Fortunato Morabito,Massimo Gentile
标识
DOI:10.1080/14712598.2024.2357382
摘要
Introduction Gain/amplification of 1q (+1q) represents one of the most prevalent cytogenetic abnormalities (CAs) observed in multiple myeloma (MM). Historical studies predating the advent of anti-CD38 monoclonal antibodies (moAbs) implicated + 1q in poor prognoses, prompting its integration into novel staging systems. However, with the emergence of daratumumab and isatuximab, two pivotal anti-CD38 moAbs, the landscape of MM therapy has undergone a profound transformation.
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