Real-world assessment of isocitrate dehydrogenase inhibitor-associated differentiation syndrome

被引:2
作者
Megherea, Oxana [1 ]
Janes, Carmen [2 ]
Kowalski, Andrew [3 ]
Baron, Jessica [4 ]
Ahn, Esther [5 ]
Soule, Ashley [6 ]
Newman, Matthew [2 ]
机构
[1] Hosp Univ Penn, Dept Pharm, 3400 Spruce St, Philadelphia, PA 19104 USA
[2] Johns Hopkins Univ Hosp, Dept Pharm, Oncol Div, Baltimore, MD 21287 USA
[3] Yale New Haven Med Ctr, Dept Pharm, 20 York St, New Haven, CT 06504 USA
[4] NewYork Presbyterian Columbia Univ, Irving Med Ctr, New York, NY USA
[5] Sibley Mem Hosp, Washington, DC USA
[6] Univ Kentucky HealthCare, Lexington, KY USA
关键词
Differentiation syndrome; IDH inhibitor; IDH-DS; acute myeloid leukemia; enasidenib; ivosidenib;
D O I
10.1080/10428194.2021.1957868
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ivosidenib and enasidenib are targeted agents that inhibit mutant isocitrate dehydrogenase (IDH) enzymes, restoring normal cellular differentiation in affected acute myeloid leukemia patients. Both agents carry a risk of differentiation syndrome (DS), a potentially life-threatening complication. In this multicenter, retrospective study we sought to determine the real-world incidence and characterize DS in patients with a myeloid malignancy treated with an IDH inhibitor. Of 49 total patients, 15 patients (31%) had a documented diagnosis of DS and 8 patients (16%) met the criteria of DS by Montesinos, et al. The most common signs and symptoms of DS were dyspnea/hypoxia (56%), unexplained fever (56%), bone pain/arthralgia (44%), edema/weight gain (39%), and pleural/pericardial effusions (33%). Our study reports a higher real-world incidence of DS in patients treated with IDH inhibitors for myeloid malignancies than previously reported.
引用
收藏
页码:3219 / 3225
页数:7
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