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疾病控制应是华氏巨球蛋白血症患者治疗的目标。

Disease control should be the goal of therapy for WM patients.

作者信息

Kastritis Efstathios, Dimopoulos Meletios A

机构信息

Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Blood Adv. 2017 Nov 28;1(25):2483-2485. doi: 10.1182/bloodadvances.2017005645.

DOI:10.1182/bloodadvances.2017005645
PMID:29296898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5729615/
Abstract

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摘要

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Ibrutinib for patients with rituximab-refractory Waldenström's macroglobulinaemia (iNNOVATE): an open-label substudy of an international, multicentre, phase 3 trial.伊布替尼治疗利妥昔单抗难治性华氏巨球蛋白血症患者(iNNOVATE):一项国际多中心 3 期临床试验的开放性亚研究。
Lancet Oncol. 2017 Feb;18(2):241-250. doi: 10.1016/S1470-2045(16)30632-5. Epub 2016 Dec 10.
2
BDR in newly diagnosed patients with WM: final analysis of a phase 2 study after a minimum follow-up of 6 years.初诊 WM 患者中的 BDR:至少随访 6 年后的 2 期研究的最终分析。
Blood. 2017 Jan 26;129(4):456-459. doi: 10.1182/blood-2016-09-742411. Epub 2016 Nov 21.
3
Allogeneic Transplantation for Relapsed Waldenström Macroglobulinemia and Lymphoplasmacytic Lymphoma.异基因移植治疗复发的华氏巨球蛋白血症和淋巴浆细胞淋巴瘤。
Biol Blood Marrow Transplant. 2017 Jan;23(1):60-66. doi: 10.1016/j.bbmt.2016.10.010. Epub 2016 Oct 24.
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Treatment recommendations from the Eighth International Workshop on Waldenström's Macroglobulinemia.瓦尔登斯特伦巨球蛋白血症第八次国际研讨会的治疗建议。
Blood. 2016 Sep 8;128(10):1321-8. doi: 10.1182/blood-2016-04-711234. Epub 2016 Jul 18.
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Dexamethasone, rituximab, and cyclophosphamide as primary treatment of Waldenström macroglobulinemia: final analysis of a phase 2 study.地塞米松、利妥昔单抗和环磷酰胺作为华氏巨球蛋白血症的一线治疗:一项2期研究的最终分析
Blood. 2015 Sep 10;126(11):1392-4. doi: 10.1182/blood-2015-05-647420.
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Competing risk survival analysis in patients with symptomatic Waldenström macroglobulinemia: the impact of disease unrelated mortality and of rituximab-based primary therapy.有症状的华氏巨球蛋白血症患者的竞争风险生存分析:疾病无关死亡率及基于利妥昔单抗的初始治疗的影响
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