Risk of intracranial hemorrhage with anticoagulation therapy in melanoma patients with brain metastases

被引:57
作者
Alvarado, Gladys [1 ]
Noor, Rahat [1 ]
Bassett, Roland [2 ]
Papadopoulos, Nicholas E. [1 ]
Kim, Kevin B. [1 ]
Hwu, Wen-Jen [1 ]
Bedikian, Agop [1 ]
Patel, Sapna [1 ]
Hwu, Patrick [1 ]
Davies, Michael A. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX 77054 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77054 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77054 USA
关键词
anticoagulation; brain metastases; intracranial hemorrhage; melanoma; venous thromboembolism; MOLECULAR-WEIGHT HEPARIN; VENOUS THROMBOEMBOLISM; CANCER-PATIENTS; CHEMOTHERAPY; THROMBOSIS; SURVIVAL; WARFARIN; GLIOMA; TUMORS;
D O I
10.1097/CMR.0b013e328353efd8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Venous thromboembolism (VTE) is a frequent complication in melanoma patients with brain metastases (BM). The management of these patients is challenging because of the high risk of intracranial hemorrhage (ICH) and the limited data available on the safety of anticoagulation in this scenario. We reviewed the treatments and outcomes among melanoma patients with BM and VTE at our institution to determine the safety of anticoagulation in these patients. A retrospective chart review was performed to identify melanoma patients with BM who were diagnosed with VTE. The clinical characteristics of the BM and the VTE, the treatments given for VTE, subsequent ICH, and overall survival (OS) were determined. The characteristics and outcomes were compared between patients who received systemic anticoagulation and those who did not. A total of 74 evaluable melanoma patients with BM and VTE were identified. Fifty-seven (77%) patients received systemic anticoagulation. There was no significant difference in the number (P=0.40) or the maximum diameter (P=0.55) of brain metastasis between the patients who received anticoagulation and those who did not. Two (4%) patients who received anticoagulation developed ICH, which was not statistically different from the patients who did not receive anticoagulation (0%, P=1.00). There was a trend toward longer OS from VTE among patients who received systemic anticoagulation (median OS: 4.2 vs. 1.2 months, P=0.06). Anticoagulation for VTE did not significantly increase the risk of ICH or decrease OS in patients with melanoma BM. These data support the safety of systemic anticoagulation for VTE in these patients. Melanoma Res 22:310-315 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:310 / 315
页数:6
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