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利妥昔单抗联合短疗程强化方案治疗伯基特淋巴瘤:疗效与安全性分析

[Rituximab combined with short-course and intensive regimen for Burkitt leukemia: efficacy and safety analysis].

作者信息

Li Y, Gong X Y, Zhao X L, Wei H, Wang Y, Lin D, Zhou C L, Liu B C, Wang H J, Li C W, Li Q H, Gong B F, Liu Y T, Wei S N, Zhang G J, Mi Y C, Wang J X, Liu K Q

机构信息

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College; State Key Laboratory of Experimental Hematology; National Clinical Research Center for Blood Diseases, Tianjin 300020, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2020 Jun 14;41(6):502-505. doi: 10.3760/cma.j.issn.0253-2727.2020.06.012.

Abstract

This study aimed to explore the efficacy and safety of rituximab combined with short-course and intensive regimens in the treatment of adult patients with Burkitt leukemia. The clinical data of 11 Burkitt leukemia patients in our hospital from January 30, 2006, to September 12, 2018, were collected. The clinical details, complete remission (CR) rate, overall survival (OS) , relapse-free survival (RFS) , and adverse events were evaluated. The median age of 11 patients was 34 (15-54) years, of which six were males and five were females (M∶F, 1.2∶1) . The median white blood cell (WBC) count was 12.28 (2.21-48.46) ×10(9)/L, and the median blast percent of peripheral blood and bone marrow were 40% (3%-76%) and 84.0% (29.5%-94.5%) , respectively. Ten patients were administered with rituximab combined with a short-course and intensive regimens, and two patients underwent autologous hematopoietic stem cell transplantation following consolidation chemotherapy. The CR rate after one cycle of induction therapy was 100%, the four-year OS was 90%, and RFS was 90%. Out of the ten treated patients, only one patient suffered from tumor lysis syndrome during the induction chemotherapy. Consequently, renal function recovered after hemodialysis and other treatments. The regimen is safe with no treatment-related deaths. Rituximab combined with short-course and intensive chemotherapy regimens is effective and well-tolerated in adult Burkitt leukemia.

摘要

本研究旨在探讨利妥昔单抗联合短疗程强化方案治疗成人伯基特白血病的疗效和安全性。收集了我院2006年1月30日至2018年9月12日期间11例伯基特白血病患者的临床资料。评估了临床细节、完全缓解(CR)率、总生存期(OS)、无复发生存期(RFS)及不良事件。11例患者的中位年龄为34(15 - 54)岁,其中男性6例,女性5例(男∶女,1.2∶1)。中位白细胞(WBC)计数为12.28(2.21 - 48.46)×10⁹/L,外周血和骨髓原始细胞百分比中位数分别为40%(3% - 76%)和84.0%(29.5% - 94.5%)。10例患者接受利妥昔单抗联合短疗程强化方案治疗,2例患者在巩固化疗后接受自体造血干细胞移植。诱导治疗1个周期后的CR率为100%,4年OS为90%,RFS为90%。10例接受治疗的患者中,仅1例在诱导化疗期间发生肿瘤溶解综合征。经血液透析及其他治疗后肾功能恢复。该方案安全,无治疗相关死亡。利妥昔单抗联合短疗程强化化疗方案治疗成人伯基特白血病有效且耐受性良好。

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Low-intensity therapy in adults with Burkitt's lymphoma.成人伯基特淋巴瘤的低强度治疗。
N Engl J Med. 2013 Nov 14;369(20):1915-25. doi: 10.1056/NEJMoa1308392.

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