Sequential autologous and allogeneic stem cell transplantation for treatment of primary plasma cell leukemia: A case report.

IF 1.4 Q4 ONCOLOGY
Weijia Fu, Aijie Huang, Yanrong Luo, Miaomiao Liu, Gusheng Tang, Jianmin Yang, Xiong Ni
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引用次数: 0

Abstract

Primary plasma cell leukemia (pPCL) is a rare and aggressive form of plasma cell disorder, which accounts for ~70% of all PCL. Survival of pPCL remains poor, and is related with early mortality. There is no standard therapy for patients with pPCL. In the present study, a 26-year-old man who was diagnosed with pPCL was reported. The patient achieved stringent complete remission to the successful treatment of intensive chemotherapy combined with sequential autologous and allogeneic stem cell transplantation (SCT) followed by maintenance therapy with oral administration of ixazomib, thalidomide and dexamethasone (IRD regimen). Development of complex treatment algorithms that combine novel agents, SCT and post-transplantation remission strategies may translate into survival in patients with pPCL.

Abstract Image

序贯自体和异体干细胞移植治疗原发性浆细胞白血病1例报告。
原发性浆细胞白血病(pPCL)是一种罕见的侵袭性浆细胞疾病,约占所有浆细胞白血病的70%。pPCL的生存率仍然很低,并与早期死亡有关。对于pPCL患者没有标准的治疗方法。在本研究中,报告了一名26岁的男性被诊断为pPCL。患者成功接受强化化疗联合顺序自体和异体干细胞移植(SCT),然后口服伊沙唑米、沙利度胺和地塞米松(IRD方案)维持治疗,达到严格的完全缓解。结合新型药物、SCT和移植后缓解策略的复杂治疗算法的发展可能会转化为pPCL患者的生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.80
自引率
0.00%
发文量
108
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