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血液单核细胞与慢性淋巴细胞白血病侵袭性及预后的关系:一项多机构研究

Relationship of blood monocytes with chronic lymphocytic leukemia aggressiveness and outcomes: a multi-institutional study.

作者信息

Friedman Daphne R, Sibley Alexander B, Owzar Kouros, Chaffee Kari G, Slager Susan, Kay Neil E, Hanson Curtis A, Ding Wei, Shanafelt Tait D, Weinberg J Brice, Wilcox Ryan A

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina.

Durham VA Medical Center, Durham, North Carolina.

出版信息

Am J Hematol. 2016 Jul;91(7):687-91. doi: 10.1002/ajh.24376. Epub 2016 Apr 24.

DOI:10.1002/ajh.24376
PMID:27037726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5137369/
Abstract

Monocyte-derived cells, constituents of the cancer microenvironment, support chronic lymphocytic leukemia (CLL) cell survival in vitro via direct cell-cell interaction and secreted factors. We hypothesized that circulating absolute monocyte count (AMC) reflects the monocyte-derived cells in the microenvironment, and that higher AMC is associated with increased CLL cell survival in vivo and thus inferior CLL patient outcomes. We assessed the extent to which AMC at diagnosis of CLL is correlated with clinical outcomes, and whether this information adds to currently used prognostic markers. We evaluated AMC, clinically used prognostic markers, and time to event data from 1,168 CLL patients followed at the Mayo Clinic, the Duke University Medical Center, and the Durham VA Medical Center. Elevated AMC was significantly associated with inferior clinical outcomes, including time to first therapy (TTT) and overall survival (OS). AMC combined with established clinical and molecular prognostic markers significantly improved risk-stratification of CLL patients for TTT. As an elevated AMC at diagnosis is associated with accelerated disease progression, and monocyte-derived cells in the CLL microenvironment promote CLL cell survival and proliferation, these findings suggest that monocytes and monocyte-derived cells are rational therapeutic targets in CLL. Am. J. Hematol. 91:687-691, 2016. © 2016 Wiley Periodicals, Inc.

摘要

单核细胞衍生细胞作为癌症微环境的组成部分,通过直接的细胞间相互作用和分泌因子在体外支持慢性淋巴细胞白血病(CLL)细胞的存活。我们推测循环绝对单核细胞计数(AMC)反映了微环境中单核细胞衍生细胞的情况,并且较高的AMC与体内CLL细胞存活率增加相关,从而导致CLL患者预后较差。我们评估了CLL诊断时AMC与临床结局的相关程度,以及该信息是否能补充目前使用的预后标志物。我们评估了梅奥诊所、杜克大学医学中心和达勒姆退伍军人事务医疗中心随访的1168例CLL患者的AMC、临床使用的预后标志物以及事件发生时间数据。AMC升高与较差的临床结局显著相关,包括首次治疗时间(TTT)和总生存期(OS)。AMC与既定的临床和分子预后标志物相结合,显著改善了CLL患者TTT的风险分层。由于诊断时AMC升高与疾病进展加速相关,且CLL微环境中的单核细胞衍生细胞促进CLL细胞存活和增殖,这些发现表明单核细胞和单核细胞衍生细胞是CLL合理的治疗靶点。《美国血液学杂志》91:687 - 691,2016年。©2016威利期刊公司

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad92/5137369/48275f2ced22/nihms825362f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad92/5137369/48275f2ced22/nihms825362f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad92/5137369/48275f2ced22/nihms825362f1.jpg

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