并发克隆性浆细胞和骨髓性疾病患者的管理:单中心描述性病例系列

IF 0.7 Q4 HEMATOLOGY
Michael J. Hochman , Gloria F. Gerber , Philip H. Imus , Syed Abbas Ali , Amy E. DeZern
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引用次数: 0

摘要

随着年龄的增长,克隆性浆细胞病和髓系疾病的发病率都会增加。同时患有克隆性浆细胞和髓细胞疾病(CPCMD)的患者会给临床和治疗带来挑战。在这个单一机构的 CPCMD 患者队列(n = 18)中,我们摘录了与临床相关的主题。大多数患者(12/18)接受了克隆导向疗法,其中三位患者接受了针对两个克隆的治疗。应优先治疗具有可靶向基因病变的克隆或引起终末器官并发症的克隆。同时治疗两个克隆可能是安全的,但最好以循序渐进的方式进行。有必要对具有双重克隆过程的患者进行进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of patients with concurrent clonal plasma cell and myeloid disorders: A single center descriptive case series

Both clonal plasma cell and myeloid disorders occur more frequently with age. Patients with concurrent clonal plasma cell and myeloid disorders (CPCMD) can present clinical and therapeutic challenges. In this single-institution cohort of patients with CPCMD (n = 18), we abstracted clinically relevant themes. A majority of patients (12/18) were treated with clone-directed therapies and three received treatment targeting both clones. Treatment of clones with targetable genetic lesions or those causing end-organ complications should be prioritized. Simultaneous treatment of both clones can be safe but is best done in a stepwise manner. Further study of patients with dual clonal processes is warranted.

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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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