Interferon decreases VEGF levels in patients with chronic myeloidleukemia treated with imatinib

被引:15
作者
Legros, L. [1 ,2 ]
Guilhot, J. [2 ,3 ]
Huault, S.
Mahon, F. X. [4 ]
Preudhomme, C. [5 ,6 ]
Guilhot, F. [3 ]
Hueber, A. O. [2 ]
机构
[1] Hop Archet 1, Serv Hematol Clin, F-06202 Nice 2, France
[2] CNRS, Inst Biol Valrose iBV, UMR 7277, UMR INSERM 1091, Nice, France
[3] CHU Poitiers, Inserm CIC 0802, Poitiers, France
[4] Univ Bordeaux Segalen, Ctr Hosp Univ Bordeaux, INSERM 1035, Lab Hematol & Serv Malad Sang,Inst Bergonie, Bordeaux, France
[5] CHU Lille, Hematol Lab, F-59037 Lille, France
[6] INSERM, U837, F-59045 Lille, France
关键词
Vascular Endothelial Growth Factor (VEGF); Imatinib; Chronic myeloid leukemia (CML); Angiogenesis; Interferon-alpha; ENDOTHELIAL GROWTH-FACTOR; CHRONIC MYELOID-LEUKEMIA; CELL GROWTH; ANGIOGENESIS; ALPHA;
D O I
10.1016/j.leukres.2014.01.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In chronic myeloid leukemia (CML), evidence is supporting the role of VEGF in growth, and survival of leukemia cells. The evaluation of plasma VEGF levels in 403 CML patients randomized within SPIRIT study to received imatinib-400 mg versus imatinib + cytarabine versus imatinib + interferon (IFN) versusimatinib-600 mg demonstrated that VEGF is an independent factor of BCR-ABL burden. VEGF low levels at diagnosis were associated with a progression-free survival of 100% at 48 months. Under treatment, significant lowest levels were observed in imatinib + IFN arm. These results support the use of VEGF as a parameter to predict CML evolution and let us to speculate about antiangiogenic properties of IFN. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:662 / 665
页数:4
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