Division of Hematology and Medical Oncology, Columbia University Irving Medical Center, NY, USA.
Expert Rev Anticancer Ther. 2021 Jun;21(6):573-581. doi: 10.1080/14737140.2021.1891885. Epub 2021 Feb 25.
Acute myeloid leukemia (AML) is an aggressive blood cancer that proves fatal for the majority of affected individuals. Older patients are particularly vulnerable due to more unfavorable disease biology and diminished ability to tolerate intensive induction chemotherapy (ICT). Safer, more efficacious therapies are desperately needed.
We briefly summarize the challenges facing AML treatment and introduce the rapidly expanding therapeutic landscape. Our focus is on the Hedgehog (Hh) pathway and how preclinical evidence has spurred the clinical development of selective inhibitors for oncology indications. Glasdegib is the first Hh pathway inhibitor approved for the treatment of a hematologic malignancy, and we review its pharmacology, safety, efficacy, and potential clinical impact in AML patients.
Advances in the mechanistic understanding of AML have started to translate into improved therapeutic options for patients with contraindications to ICT. Glasdegib improved overall survival in this population when combined with low-dose cytarabine. While an encouraging development for these difficult to treat patients, alternative combination therapy approaches such as venetoclax plus azacitidine have gained greater clinical traction. Further investigation of glasdegib combination strategies and predictive biomarkers, particularly in regard to overcoming chemoresistance and preventing relapse, is needed to better define its clinical utility.
急性髓细胞白血病(AML)是一种侵袭性血液癌症,大多数受影响的个体都因此死亡。由于疾病生物学更不利,以及耐受强化诱导化疗(ICT)的能力降低,老年患者尤其容易受到影响。迫切需要更安全、更有效的治疗方法。
我们简要总结了 AML 治疗面临的挑战,并介绍了快速扩展的治疗领域。我们的重点是 Hedgehog(Hh)途径,以及临床前证据如何激发了针对肿瘤适应症的选择性抑制剂的临床开发。glasdegib 是第一个获批用于治疗血液系统恶性肿瘤的 Hh 途径抑制剂,我们回顾了其在 AML 患者中的药理学、安全性、疗效和潜在临床影响。
对 AML 发病机制的理解的进步已经开始转化为对 ICT 禁忌患者的治疗选择的改善。当与低剂量阿糖胞苷联合使用时,glasdegib 改善了这些患者的总生存期。虽然这对这些难以治疗的患者来说是一个令人鼓舞的发展,但替代联合治疗方法,如 venetoclax 加阿扎胞苷,已获得更大的临床关注。需要进一步研究 glasdegib 联合治疗策略和预测生物标志物,特别是在克服化疗耐药性和预防复发方面,以更好地确定其临床应用。