Cassier Philippe A, Castets Marie, Belhabri Amine, Vey Norbert
Department of Medical Oncology, Centre Léon Bérard, 69008 Lyon, France.
Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, 69008 Lyon, France.
Br J Cancer. 2017 Oct 10;117(8):1089-1098. doi: 10.1038/bjc.2017.281. Epub 2017 Aug 24.
Acute myeloid leukaemia (AML) is a molecularly and clinically heterogeneous disease, and its incidence is increasing as the populations in Western countries age. Despite major advances in understanding the genetic landscape of AML and its impact on the biology of the disease, standard therapy has not changed significantly in the last three decades. Allogeneic haematopoietic stem cell transplantation remains the best chance for cure, but can only be offered to a minority of younger fit patients. Molecularly targeted drugs aiming at restoring apoptosis in leukaemic cells have shown encouraging activity in early clinical trials and some of these drugs are currently being evaluated in randomised controlled trials. In this review, we discuss the current development of drugs designed to trigger cell death in AML.
急性髓系白血病(AML)是一种在分子和临床方面具有异质性的疾病,随着西方国家人口老龄化,其发病率正在上升。尽管在了解AML的基因图谱及其对疾病生物学的影响方面取得了重大进展,但在过去三十年中,标准疗法并没有显著改变。异基因造血干细胞移植仍然是治愈的最佳机会,但只能提供给少数年轻健康的患者。旨在恢复白血病细胞凋亡的分子靶向药物在早期临床试验中显示出令人鼓舞的活性,目前其中一些药物正在随机对照试验中进行评估。在这篇综述中,我们讨论了旨在引发AML细胞死亡的药物的当前进展。