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CXCL13 levels are elevated in patients with Waldenström macroglobulinemia, and are predictive of major response to ibrutinib.

作者信息

Vos Josephine M, Tsakmaklis Nickolas, Patterson Christopher J, Meid Kirsten, Castillo Jorge J, Brodsky Philip, Ganz Tomas, Pals Steven T, Kersten Marie José, Xu Lian, Yang Guang, Treon Steven P, Hunter Zachary R

机构信息

St. Antonius Hospital, Nieuwegein, The Netherlands

Bing Center for WM, Dana Farber Cancer Insitute, Boston, MA, USA.

出版信息

Haematologica. 2017 Nov;102(11):e452-e455. doi: 10.3324/haematol.2017.172627. Epub 2017 Aug 10.

Abstract
摘要

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本文引用的文献

1
Transcriptome sequencing reveals a profile that corresponds to genomic variants in Waldenström macroglobulinemia.
Blood. 2016 Aug 11;128(6):827-38. doi: 10.1182/blood-2016-03-708263. Epub 2016 Jun 14.
3
Clonal architecture of CXCR4 WHIM-like mutations in Waldenström Macroglobulinaemia.
Br J Haematol. 2016 Mar;172(5):735-44. doi: 10.1111/bjh.13897. Epub 2015 Dec 13.
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MYD88 Mutations and Response to Ibrutinib in Waldenström's Macroglobulinemia.
N Engl J Med. 2015 Aug 6;373(6):584-6. doi: 10.1056/NEJMc1506192.
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Ibrutinib in previously treated Waldenström's macroglobulinemia.
N Engl J Med. 2015 Apr 9;372(15):1430-40. doi: 10.1056/NEJMoa1501548.
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Response assessment in Waldenström macroglobulinaemia: update from the VIth International Workshop.
Br J Haematol. 2013 Jan;160(2):171-6. doi: 10.1111/bjh.12102. Epub 2012 Nov 15.
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MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.
N Engl J Med. 2012 Aug 30;367(9):826-33. doi: 10.1056/NEJMoa1200710.

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