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新诊断多发性骨髓瘤诱导治疗期间未受累免疫球蛋白的变化

Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma.

作者信息

Ravi P, Kumar S, Gonsalves W, Buadi F, Lacy M Q, Go R S, Dispenzieri A, Kapoor P, Lust J A, Dingli D, Lin Y, Russell S J, Leung N, Gertz M A, Kyle R A, Bergsagel P L, Rajkumar S V

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

出版信息

Blood Cancer J. 2017 Jun 16;7(6):e569. doi: 10.1038/bcj.2017.46.

DOI:10.1038/bcj.2017.46
PMID:28622306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5584483/
Abstract

Little is known about the impact of multiple myeloma (MM) treatment on uninvolved immunoglobulins (Ig). We identified 448 patients who received high-dose dexamethasone (HD-DEX), lenalidomide and dexamethasone (RD), bortezomib and dexamethasone (VD), bortezomib, cyclophosphamide and dexamethasone (VCD) or bortezomib, lenalidomide and dexamethasone (VRD) for newly diagnosed MM at our institution between 2000 and 2013, and who had available data on absolute lymphocyte count (ALC) and quantitative uninvolved Ig at baseline and at the end of four cycles of therapy. Changes in ALC and uninvolved Ig were significantly different across treatments, with VCD and HD-DEX producing reductions in uninvolved Ig, and RD, VD and VRD leading to increases in uninvolved Ig. In addition, treatment with RD, VD and VRD was independently associated with higher odds of achieving a ⩾25% increase in or normalization of the primary uninvolved Ig on multivariate analysis. Although achievement of a humoral response in the primary uninvolved Ig was associated with a higher odds of achieving VGPR or better after four cycles of therapy, it was not associated with improved overall survival. These data highlight the different mechanisms of action of MM drugs and point toward a possible role for the use of VCD in treating antibody-mediated autoimmune disease.

摘要

关于多发性骨髓瘤(MM)治疗对未受累免疫球蛋白(Ig)的影响,人们了解甚少。我们确定了448例于2000年至2013年在本机构接受高剂量地塞米松(HD-DEX)、来那度胺和地塞米松(RD)、硼替佐米和地塞米松(VD)、硼替佐米、环磷酰胺和地塞米松(VCD)或硼替佐米、来那度胺和地塞米松(VRD)治疗的新诊断MM患者,这些患者在基线及四个治疗周期结束时均有绝对淋巴细胞计数(ALC)和定量未受累Ig的可用数据。不同治疗方案中ALC和未受累Ig的变化存在显著差异,VCD和HD-DEX导致未受累Ig降低,而RD、VD和VRD则使未受累Ig升高。此外,在多变量分析中,RD、VD和VRD治疗与主要未受累Ig增加≥25%或恢复正常的较高几率独立相关。虽然在四个治疗周期后,主要未受累Ig出现体液反应与达到VGPR或更好疗效的较高几率相关,但与总体生存率的改善无关。这些数据突出了MM药物不同的作用机制,并表明VCD在治疗抗体介导的自身免疫性疾病中可能发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/c33fc9f60033/bcj201746f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/97d2239750b3/bcj201746f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/135adc45f28c/bcj201746f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/c33fc9f60033/bcj201746f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/97d2239750b3/bcj201746f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/135adc45f28c/bcj201746f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08a/5584483/c33fc9f60033/bcj201746f3.jpg

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