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利妥昔单抗用于B细胞非霍奇金淋巴瘤患者自体干细胞移植后的长期维持治疗。

Rituximab long-term maintenance therapy after autologous stem cell transplantation in patients with B-cell non-Hodgkin's lymphoma.

作者信息

Neumann Frank, Harmsen Stefani, Martin Simona, Kronenwett Ralf, Kondakci Mustafa, Aivado Manuel, Germing Ulrich, Haas Rainer, Kobbe Guido

机构信息

Department of Hematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Duesseldorf Moorenstr. 5, 40225, Duesseldorf, Germany.

出版信息

Ann Hematol. 2006 Aug;85(8):530-4. doi: 10.1007/s00277-006-0113-5. Epub 2006 Apr 26.

DOI:10.1007/s00277-006-0113-5
PMID:16639571
Abstract

Treatment of B-cell non-Hodgkin's lymphomas (NHL) with either Rituximab alone or in combination with cytotoxic chemotherapy has been effective without major side effects. Thus, Rituximab maintenance therapy after autologous peripheral blood stem cell transplantation (PBSCT) might represent an improvement in NHL therapy. We therefore retrospectively analyzed the efficacy and side effects of monthly long-term Rituximab maintenance therapy after PBSCT in 27 patients with NHL. In median 10 infusions of Rituximab were given after PBSCT in time intervals of 1 month. Molecular monitoring of t(14;18) was performed using nested as well as quantitative real time polymerase chain reaction (RT-PCR) based on the LightCycler technology. Side effects according to common toxicity criteria (CTC) > II did mainly affect the hematopoietic system. In total, 10 patients (37%) suffered form grade III-IV hematotoxicity. Except for two patients with cutaneous Varicella-Zoster infection no serious infectious complications (CTC grade III/IV) occurred. No patient died because of treatment-related causes. This adverse event data compared favorably to the published data. Three patients had t(14;18) nested RT-PCR positive results before Rituximab therapy and converted to negativity after Rituximab therapy. We conclude that a prolonged Rituximab maintenance therapy after PBSCT with monthly administration is reliable and safe.

摘要

单独使用利妥昔单抗或与细胞毒性化疗联合治疗B细胞非霍奇金淋巴瘤(NHL)已取得疗效,且无严重副作用。因此,自体外周血干细胞移植(PBSCT)后进行利妥昔单抗维持治疗可能会改善NHL的治疗效果。我们因此回顾性分析了27例NHL患者在PBSCT后每月进行长期利妥昔单抗维持治疗的疗效和副作用。PBSCT后,中位进行了10次利妥昔单抗输注,时间间隔为1个月。基于LightCycler技术,采用巢式及定量实时聚合酶链反应(RT-PCR)对t(14;18)进行分子监测。根据常见毒性标准(CTC)> II级的副作用主要影响造血系统。共有10例患者(37%)出现III-IV级血液毒性。除2例皮肤水痘-带状疱疹感染患者外,未发生严重感染并发症(CTC III/IV级)。无患者因治疗相关原因死亡。该不良事件数据与已发表数据相比更优。3例患者在利妥昔单抗治疗前t(14;18)巢式RT-PCR检测结果为阳性,治疗后转为阴性。我们得出结论,PBSCT后每月进行延长的利妥昔单抗维持治疗是可靠且安全的。

相似文献

1
Rituximab long-term maintenance therapy after autologous stem cell transplantation in patients with B-cell non-Hodgkin's lymphoma.利妥昔单抗用于B细胞非霍奇金淋巴瘤患者自体干细胞移植后的长期维持治疗。
Ann Hematol. 2006 Aug;85(8):530-4. doi: 10.1007/s00277-006-0113-5. Epub 2006 Apr 26.
2
Rituximab does not compromise the mobilization and engraftment of autologous peripheral blood stem cells in diffuse-large B-cell lymphoma.利妥昔单抗不会损害弥漫性大B细胞淋巴瘤患者自体外周血干细胞的动员和植入。
Bone Marrow Transplant. 2007 May;39(9):523-7. doi: 10.1038/sj.bmt.1705649. Epub 2007 Mar 19.
3
Effect of rituximab on the long-term outcome after high-dose therapy for relapsed B-cell non-Hodgkin's lymphoma.利妥昔单抗对复发B细胞非霍奇金淋巴瘤大剂量治疗后长期预后的影响。
Ann Hematol. 2006 Nov;85(11):769-79. doi: 10.1007/s00277-006-0157-6. Epub 2006 Aug 1.
4
Adjuvant rituximab causes prolonged hypogammaglobulinaemia following autologous stem cell transplant for non-Hodgkin's lymphoma.对于非霍奇金淋巴瘤患者,自体干细胞移植后使用利妥昔单抗辅助治疗会导致长时间的低丙种球蛋白血症。
Bone Marrow Transplant. 2006 Sep;38(6):433-6. doi: 10.1038/sj.bmt.1705463. Epub 2006 Aug 7.
5
Rituximab therapy increased post-transplant cytomegalovirus complications in Non-Hodgkin's lymphoma patients receiving autologous hematopoietic stem cell transplantation.利妥昔单抗治疗增加了接受自体造血干细胞移植的非霍奇金淋巴瘤患者移植后的巨细胞病毒并发症。
Ann Hematol. 2008 Apr;87(4):285-9. doi: 10.1007/s00277-007-0397-0. Epub 2007 Oct 18.
6
[Use of Mabtera (rituximab) in treating patients with refractory courses of B-cell lymphoma, along with high-dose chemotherapy and autologous transplantation of hematopoietic stem cells].[美罗华(利妥昔单抗)联合大剂量化疗及自体造血干细胞移植用于治疗难治性B细胞淋巴瘤患者]
Ter Arkh. 2003;75(1):65-8.
7
High-dose therapy supported with immunomagnetic purged autologous bone marrow in high-grade B cell non-Hodgkin's lymphoma.高剂量疗法联合免疫磁珠净化的自体骨髓用于高级别B细胞非霍奇金淋巴瘤的治疗
Bone Marrow Transplant. 1999 Oct;24(8):865-72. doi: 10.1038/sj.bmt.1701990.
8
Rituximab in vivo purging is safe and effective in combination with CD34-positive selected autologous stem cell transplantation for salvage therapy in B-NHL.利妥昔单抗体内净化联合CD34阳性选择的自体干细胞移植用于B-NHL挽救治疗是安全有效的。
Bone Marrow Transplant. 2002 May;29(9):769-75. doi: 10.1038/sj.bmt.1703515.
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Rituximab induces effective clearance of minimal residual disease in molecular relapses of mantle cell lymphoma.利妥昔单抗可有效清除套细胞淋巴瘤分子复发时的微小残留病灶。
Biol Blood Marrow Transplant. 2006 Dec;12(12):1270-6. doi: 10.1016/j.bbmt.2006.07.007.
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Combination immunotherapy of B-cell non-Hodgkin's lymphoma with rituximab and interleukin-2: a preclinical and phase I study.利妥昔单抗与白细胞介素-2联合免疫治疗B细胞非霍奇金淋巴瘤:一项临床前及I期研究。
Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6101-10. doi: 10.1158/1078-0432.CCR-04-0525.

引用本文的文献

1
Postulated mechanisms of resistance of B-cell non-Hodgkin lymphoma to rituximab treatment regimens: strategies to overcome resistance.B细胞非霍奇金淋巴瘤对利妥昔单抗治疗方案耐药的假定机制:克服耐药的策略。
Semin Oncol. 2014 Oct;41(5):667-77. doi: 10.1053/j.seminoncol.2014.08.006. Epub 2014 Aug 12.
2
Incidence of hypogammaglobulinemia in patients receiving rituximab and the use of intravenous immunoglobulin for recurrent infections.利妥昔单抗治疗患者低丙种球蛋白血症的发生率和静脉用免疫球蛋白治疗复发性感染的应用。
Clin Lymphoma Myeloma Leuk. 2013 Apr;13(2):106-11. doi: 10.1016/j.clml.2012.11.011. Epub 2012 Dec 29.
3
Rituximab in the treatment of B-cell non-Hodgkin lymphoma, focus on outcomes and comparative effectiveness.
利妥昔单抗治疗B细胞非霍奇金淋巴瘤,重点关注疗效和比较效果。
Clinicoecon Outcomes Res. 2010;2:37-45. doi: 10.2147/ceor.s4221. Epub 2010 Apr 7.
4
Rituximab resistance.利妥昔单抗耐药。
Best Pract Res Clin Haematol. 2011 Jun;24(2):203-16. doi: 10.1016/j.beha.2011.02.009. Epub 2011 Apr 13.
5
The role of rituximab in autologous and allogeneic hematopoietic stem cell transplantation for non-Hodgkin's lymphoma.利妥昔单抗在非霍奇金淋巴瘤的自体和异基因造血干细胞移植中的作用。
Curr Hematol Malig Rep. 2006 Dec;1(4):220-9. doi: 10.1007/s11899-006-0003-x.