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PRIMA-1Met induces apoptosis in Waldenström's Macroglobulinemia cells independent of p53.PRIMA-1Met可诱导华氏巨球蛋白血症细胞凋亡,且不依赖于p53。
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本文引用的文献

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Incidence of therapy-related myeloid neoplasia after initial therapy for chronic lymphocytic leukemia with fludarabine-cyclophosphamide versus fludarabine: long-term follow-up of US Intergroup Study E2997.氟达拉滨-环磷酰胺与氟达拉滨初始治疗慢性淋巴细胞白血病后治疗相关髓系肿瘤的发生率:美国 E2997 协作组研究的长期随访。
Blood. 2011 Sep 29;118(13):3525-7. doi: 10.1182/blood-2011-03-342485. Epub 2011 Jul 29.
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Fludarabine plus cyclophosphamide and rituximab in Waldenstrom macroglobulinemia: an effective but myelosuppressive regimen to be offered to patients with advanced disease.氟达拉滨联合环磷酰胺和利妥昔单抗治疗巨球蛋白血症:一种有效但骨髓抑制的方案,适用于晚期疾病患者。
Cancer. 2012 Jan 15;118(2):434-43. doi: 10.1002/cncr.26303. Epub 2011 Jul 5.
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Chemoimmunotherapy with fludarabine and rituximab produces extended overall survival and progression-free survival in chronic lymphocytic leukemia: long-term follow-up of CALGB study 9712.氟达拉滨和利妥昔单抗的化疗免疫治疗可延长慢性淋巴细胞白血病的总生存期和无进展生存期:CALGB 研究 9712 的长期随访。
J Clin Oncol. 2011 Apr 1;29(10):1349-55. doi: 10.1200/JCO.2010.31.1811. Epub 2011 Feb 14.
4
Fludarabine, cyclophosphamide, and rituximab chemoimmunotherapy is highly effective treatment for relapsed patients with CLL.氟达拉滨、环磷酰胺和利妥昔单抗化疗免疫治疗是治疗 CLL 复发患者的非常有效方法。
Blood. 2011 Mar 17;117(11):3016-24. doi: 10.1182/blood-2010-08-304683. Epub 2011 Jan 18.
5
Autologous hematopoietic stem cell transplantation in chronic lymphocytic leukemia: results of European intergroup randomized trial comparing autografting versus observation.自体造血干细胞移植治疗慢性淋巴细胞白血病:欧洲多中心随机对照试验比较自体移植与观察的结果。
Blood. 2011 Feb 3;117(5):1516-21. doi: 10.1182/blood-2010-09-308775. Epub 2010 Nov 24.
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Therapy-related myelodysplastic syndrome and acute myeloid leukemia following fludarabine combination chemotherapy.氟达拉滨联合化疗后相关性骨髓增生异常综合征和急性髓系白血病。
Leukemia. 2010 Dec;24(12):2056-62. doi: 10.1038/leu.2010.218. Epub 2010 Oct 21.
7
Addition of rituximab to fludarabine and cyclophosphamide in patients with chronic lymphocytic leukaemia: a randomised, open-label, phase 3 trial.利妥昔单抗联合氟达拉滨和环磷酰胺治疗慢性淋巴细胞白血病患者的随机、开放标签、3 期临床试验。
Lancet. 2010 Oct 2;376(9747):1164-74. doi: 10.1016/S0140-6736(10)61381-5.
8
Rituximab and subcutaneous 2-chloro-2'-deoxyadenosine combination treatment for patients with Waldenstrom macroglobulinemia: clinical and biologic results of a phase II multicenter study.利妥昔单抗联合皮下注射 2-氯-2'-脱氧腺苷治疗华氏巨球蛋白血症患者:一项 II 期多中心研究的临床和生物学结果。
J Clin Oncol. 2010 May 1;28(13):2233-8. doi: 10.1200/JCO.2009.23.6315. Epub 2010 Apr 5.
9
Incidence and susceptibility to therapy-related myeloid neoplasms.治疗相关髓系肿瘤的发生率和易感性。
Chem Biol Interact. 2010 Mar 19;184(1-2):39-45. doi: 10.1016/j.cbi.2009.12.013. Epub 2009 Dec 21.
10
Epigenetic changes in therapy-related MDS/AML.治疗相关性 MDS/AML 中的表观遗传学改变。
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慢性淋巴细胞白血病和华氏巨球蛋白血症中的治疗相关髓系肿瘤。

Therapy-Related Myeloid Neoplasms in Chronic Lymphocytic Leukemia and Waldenstrom's Macroglobulinemia.

机构信息

Division of Hematology, Niguarda Ca' Granda Hospital, Milano, Italy.

出版信息

Mediterr J Hematol Infect Dis. 2011;3(1):e2011031. doi: 10.4084/MJHID.2011.031. Epub 2011 Jul 9.

DOI:10.4084/MJHID.2011.031
PMID:21869917
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3152453/
Abstract

Secondary myelodysplasia (MDS) and acute myeloid leukemia (AML) are frequent long term complications in Chronic Lymphocytic Leukemia (CLL) and Waldenström Macroglobulinemia (WM) patients. Although disease-related immune-suppression plays a crucial role in leukemogenesis there is great concern that therapy may further increase the risk of developing these devastating complications.Nucleoside analogs (NA) and alkylating agents are considered appropriate agents in the treatment of both CLL and WM patients. Prolonged immunosuppression related to NA therapy and the incorporation of these agents or their metabolites into DNA, with potentially mutagenic action, leads to speculation that their therapeutic use might be responsible for an increased incidence of second cancer especially when combined with other DNA damaging agents like alkylating agents.In this review the published studies considering the occurrence of secondary MDS and AML in CLL and WM patients are reported and the potential role of chemotherapeutic agents in leukemogenesis is discussed.

摘要

继发性骨髓增生异常综合征(MDS)和急性髓系白血病(AML)是慢性淋巴细胞白血病(CLL)和华氏巨球蛋白血症(WM)患者的常见长期并发症。虽然疾病相关的免疫抑制在白血病发生中起着至关重要的作用,但人们非常担心治疗可能会进一步增加发生这些毁灭性并发症的风险。核苷类似物(NA)和烷化剂被认为是 CLL 和 WM 患者治疗的合适药物。与 NA 治疗相关的长期免疫抑制以及这些药物或其代谢物掺入 DNA 中,具有潜在的诱变作用,这导致人们推测它们的治疗用途可能会导致第二癌症的发生率增加,尤其是当与其他 DNA 损伤剂如烷化剂联合使用时。在这篇综述中,报告了考虑 CLL 和 WM 患者继发性 MDS 和 AML 发生的已发表研究,并讨论了化疗药物在白血病发生中的潜在作用。