Oral therapy for myelodysplastic syndromes/neoplasms and acute myeloid leukemia: a revolution in progress

被引:2
|
作者
Venugopal, Sangeetha [1 ]
Shallis, Rory M. M. [1 ]
Zeidan, Amer M. M. [2 ]
机构
[1] Univ Miami, Sylvester Comprehens Canc Ctr, Div Hematol, Miami, FL USA
[2] Yale Sch Med, Dept Internal Med, Sect Hematol, New Haven, CT 06510 USA
关键词
AML; MDS; C-DEC; CC486; venetoclax; gilteritinib; ivosidenib; olutasidenib; TRANSFUSION-DEPENDENT PATIENTS; PHASE-III; DECITABINE/CEDAZURIDINE ASTX727; RANDOMIZED PHASE-3; SCORING SYSTEM; LENALIDOMIDE; AZACITIDINE; ENASIDENIB; PLACEBO; ELTROMBOPAG;
D O I
10.1080/14737140.2023.2238897
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IntroductionPatients with myeloid neoplasms such as myelodysplastic syndromes/neoplasms (MDS) and acute myeloid leukemia (AML) are generally older, and many are not eligible for curative intent intensive therapies and/or allogeneic hematopoietic stem cell transplantation. While lower intensity, hypomethylating agent (HMA)-based therapies such as azacitidine+venetoclax have improved patient outcomes significantly, responses are not durable, and most patients die from disease-related complications. The approvals of oral HMAs such as cedazuridine-decitabine (C-DEC) and oral azacitidine (CC-486) have kindled the hope that myeloid malignancies may soon be treated with total oral therapy.Areas coveredWe review all-oral therapies including the approvals of C-DEC and CC-486 in MDS and AML, respectively, in addition to emerging all-oral therapies, both monotherapy and combination, in higher-risk (HR) MDS and AML.Expert opinionOral HMAs have the potential to be a convenient and efficacy-equivalent treatment option for patients with HR-MDS or AML and improve their quality of life by reducing clinic visits for medication administration. Total-oral therapy combinations, largely including an oral HMA 'backbone,' are in the early phases of clinical development, and it is our hope that well-designed trials employing these agents may soon allow the identification of optimal regimens that deliver effective disease-directed therapy with good tolerability.
引用
收藏
页码:903 / 911
页数:9
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