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用于继发性骨髓增生异常综合征(MDS)/急性髓系白血病(AML)合并实体瘤复发儿童的表观遗传联合疗法

Epigenetic Combination Therapy for Children With Secondary Myelodysplastic Syndrome (MDS)/Acute Myeloid Leukemia (AML) and Concurrent Solid Tumor Relapse.

作者信息

Glasser Chana L, Lee Alice, Eslin Don, Marks Lianna, Modak Shakeel, Glade Bender Julia L

机构信息

*Department of Pediatric Hematology/Oncology, Winthrop University Medical Center, Mineola †Department of Pediatric Hematology/Oncology/Stem Cell Transplantation, Columbia University Medical Center, New York Presbyterian Hospital §Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY ‡Department of Pediatric Hematology/Oncology, Arnold Palmer Hospital for Children, Orlando, FL.

出版信息

J Pediatr Hematol Oncol. 2017 Oct;39(7):560-564. doi: 10.1097/MPH.0000000000000868.

Abstract

Secondary myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) is a rare but devastating complication of solid tumor treatment involving high-dose topoisomerase II inhibitor and alkylator chemotherapy. For relapsed or elderly MDS and AML patients ineligible for hematopoietic stem cell transplantation, epigenetic therapies, including DNA methyltransferase inhibitors and histone deacetylase inhibitors, have been utilized as palliative therapy, offering a well-tolerated approach to disease stabilization, prolonged survival, and quality of life. Literature on the use of epigenetic therapies for both primary and relapsed disease is scarce in the pediatric population. Here, we report 2 pediatric patients with secondary AML and MDS, respectively, due to prior therapy for metastatic solid tumors. Both patients were ineligible for hematopoietic stem cell transplantation due to concurrent solid tumor relapse, but were treated with the epigenetic combination therapy, decitabine and vorinostat, and achieved stabilization of marrow disease, outpatient palliation, and family-reported reasonable quality of life.

摘要

继发性骨髓增生异常综合征(MDS)/急性髓系白血病(AML)是实体瘤治疗中一种罕见但具有毁灭性的并发症,涉及大剂量拓扑异构酶II抑制剂和烷化剂化疗。对于不符合造血干细胞移植条件的复发或老年MDS和AML患者,表观遗传疗法,包括DNA甲基转移酶抑制剂和组蛋白脱乙酰酶抑制剂,已被用作姑息治疗,为疾病稳定、延长生存期和提高生活质量提供了一种耐受性良好的方法。在儿科人群中,关于表观遗传疗法用于原发性和复发性疾病的文献很少。在此,我们报告2例分别因先前转移性实体瘤治疗而继发AML和MDS的儿科患者。由于同时发生实体瘤复发,这两名患者均不符合造血干细胞移植条件,但接受了地西他滨和伏立诺他的表观遗传联合治疗,实现了骨髓疾病稳定、门诊姑息治疗以及家庭报告的合理生活质量。

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