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1
Risk of second primary malignancy in patients with AL amyloidosis treated with lenalidomide.接受来那度胺治疗的 AL 淀粉样变性患者发生第二原发性恶性肿瘤的风险。
Am J Hematol. 2013 Aug;88(8):719. doi: 10.1002/ajh.23470. Epub 2013 May 30.
2
A phase II trial of cyclophosphamide, lenalidomide and dexamethasone in previously treated patients with AL amyloidosis.一项在既往接受治疗的淀粉样变性病患者中应用环磷酰胺、来那度胺和地塞米松的 II 期临床试验。
Haematologica. 2013 Mar;98(3):433-6. doi: 10.3324/haematol.2012.073593. Epub 2012 Sep 14.
3
Continuous lenalidomide treatment for newly diagnosed multiple myeloma.来那度胺持续治疗新诊断的多发性骨髓瘤。
N Engl J Med. 2012 May 10;366(19):1759-69. doi: 10.1056/NEJMoa1112704.
4
Lenalidomide, cyclophosphamide, and dexamethasone (CRd) for light-chain amyloidosis: long-term results from a phase 2 trial.来那度胺、环磷酰胺和地塞米松(CRd)治疗轻链淀粉样变性:来自一项 2 期试验的长期结果。
Blood. 2012 May 24;119(21):4860-7. doi: 10.1182/blood-2012-01-407791. Epub 2012 Apr 13.
5
A review of second primary malignancy in patients with relapsed or refractory multiple myeloma treated with lenalidomide.来那度胺治疗复发/难治性多发性骨髓瘤患者的第二原发性恶性肿瘤回顾。
Blood. 2012 Mar 22;119(12):2764-7. doi: 10.1182/blood-2011-08-373514. Epub 2012 Feb 9.
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Risk of acute myeloid leukemia and myelodysplastic syndromes after multiple myeloma and its precursor disease (MGUS).多发性骨髓瘤及其前体疾病(MGUS)后发生急性髓系白血病和骨髓增生异常综合征的风险。
Blood. 2011 Oct 13;118(15):4086-92. doi: 10.1182/blood-2011-05-355743. Epub 2011 Jul 27.
7
Risk of second cancers in Waldenström macroglobulinemia.华氏巨球蛋白血症的二次癌症风险。
Ann Oncol. 2012 Feb;23(2):411-5. doi: 10.1093/annonc/mdr119. Epub 2011 Apr 27.
8
Transformation of the 5q- syndrome to acute lymphoblastic leukemia: a report of two cases and review of the literature.5q-综合征转化为急性淋巴细胞白血病:两例报告并文献复习
Int J Clin Exp Pathol. 2011 Mar;4(3):322-6. Epub 2011 Mar 22.
9
Lenalidomide in combination with melphalan and dexamethasone in patients with newly diagnosed AL amyloidosis: a multicenter phase 1/2 dose-escalation study.来那度胺联合美法仑和地塞米松治疗新诊断的淀粉样变性病患者:一项多中心 1/2 期剂量递增的研究。
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10
How I treat Waldenström macroglobulinemia.我如何治疗华氏巨球蛋白血症。
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一例使用来那度胺治疗的轻链(AL)淀粉样变性患者并发急性淋巴细胞白血病的罕见病例。

A rare case of acute lymphoblastic leukemia in a patient with light chain (AL) amyloidosis treated with lenalidomide.

作者信息

Nair Ranjit, Gheith Shereen, Popescu Dan, Agostino Nicole M

机构信息

Department of Internal Medicine, Lehigh Valley Hospital and Health Network Allentown, PA 18105, USA.

Department of Pathology, Lehigh Valley Hospital and Health Network Allentown, PA 18105, USA.

出版信息

Int J Clin Exp Pathol. 2014 Apr 15;7(5):2683-9. eCollection 2014.

PMID:24966987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4069899/
Abstract

Lenalidomide belongs to a novel class of drugs called Immunomodulators which are now being used for the treatment of plasma cell dyscrasias with variable degrees of efficacy and toxicity. Though Second Primary Malignancies (SPM) have been a concern with its use, the benefits of the treatment outweigh the risks. The leukemogenic risk seems to be potentiated especially when combined with alkylating agents and the SPMs documented are predominantly myeloblastic. To date there are no reported cases of new lymphocytic leukemias in AL amyloidosis, regardless of whether undergone treatment or not. We present a case of AL amylodosis who was treated with lenalidomide and subsequently developed acute lymphoblastic leukemia.

摘要

来那度胺属于一类名为免疫调节剂的新型药物,目前正用于治疗浆细胞发育异常,疗效和毒性程度各异。尽管使用该药物一直存在继发性原发性恶性肿瘤(SPM)的问题,但治疗的益处大于风险。尤其是与烷化剂联合使用时,白血病发生风险似乎会增加,且记录在案的SPM主要为成髓细胞性。迄今为止,无论是否接受过治疗,在AL淀粉样变性中均未报告有新的淋巴细胞白血病病例。我们报告一例接受来那度胺治疗的AL淀粉样变性患者,随后发生了急性淋巴细胞白血病。