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VEGFR2和诱导型一氧化氮合酶免疫组化表达在脊柱脊索瘤中的预后意义

Prognostic significance of immunohistochemical expression of VEGFR2 and iNOS in spinal chordoma.

作者信息

Akhavan-Sigari Reza, Gaab Michael Robert, Rohde Veit, Abili Mehdi, Ostertag Helmut

机构信息

Department of Neurosurgery, University Medical Center Göttingen, Georg-August-University Göttingen, Robert-Koch-Strasse 40, 37075, Göttingen, Germany,

出版信息

Eur Spine J. 2014 Nov;23(11):2416-22. doi: 10.1007/s00586-014-3417-5. Epub 2014 Jun 15.

DOI:10.1007/s00586-014-3417-5
PMID:24929808
Abstract

PURPOSE

To clarify whether vascular endothelial growth factor receptor 2 (VEGFR2) and inducible nitric oxide synthase (iNOS) are involved in the angiogenesis and recurrence of spinal chordoma tissues and influence the overall survival.

METHODS

All patients affected by a spinal chordoma surgically treated between 1986 and 2007 were reviewed. We examined the expression of VEGFR2 and iNOS with immunohistochemistry using a tissue microarray containing 120 chordoma samples. Local recurrence and overall survival (OS) were analyzed.

RESULTS

A series of 40 chordoma patients who underwent surgery for a total of 120 lesions (including 80 recurrent lesions) were identified (sacrum 77.5 %, lumbar spine 17.5 %, cervical/thoracic spine 5 %). Surgical margins were wide in 30 (75 %), marginal in 8 (20 %) and intralesional in 2 (5 %) patients. Median follow-up was 120 months. The 5- and 10-year OS of the entire series of patients was 78.6 and 30 %, respectively. There were five primary chordomas (12.5 %) with moderate and 35 (87.5 %) with strong expression of VEGFR-2. All recurrent spinal chordomas displayed strong expression of VEGFR-2. The expression of iNOS was predominately moderate to high in primary chordomas: There were 15 tumors (37.5 %) with moderate and 25 tumors (62.5 %) with strong expression. All recurrent chordomas displayed strong expression of iNOS.

CONCLUSION

The high expression of VEGFR-2 and iNOS affected the OS. The OS at 10 years was only 30 %.

摘要

目的

阐明血管内皮生长因子受体2(VEGFR2)和诱导型一氧化氮合酶(iNOS)是否参与脊索瘤组织的血管生成和复发,并影响总生存期。

方法

回顾了1986年至2007年间接受手术治疗的所有脊索瘤患者。我们使用包含120个脊索瘤样本的组织芯片,通过免疫组织化学检测VEGFR2和iNOS的表达。分析局部复发和总生存期(OS)。

结果

确定了40例脊索瘤患者,共进行了120次手术(包括80次复发病变)(骶骨77.5%,腰椎17.5%,颈椎/胸椎5%)。30例(75%)患者手术切缘为广泛切除,8例(20%)为边缘切除,2例(5%)为病损内切除。中位随访时间为120个月。整个系列患者的5年和10年总生存率分别为78.6%和30%。有5例原发性脊索瘤(12.5%)VEGFR-2表达为中度,35例(87.5%)为强表达。所有复发性脊索瘤均显示VEGFR-2强表达。原发性脊索瘤中iNOS的表达主要为中度至高表达:15例肿瘤(37.5%)为中度表达,25例肿瘤(62.5%)为强表达。所有复发性脊索瘤均显示iNOS强表达。

结论

VEGFR-2和iNOS的高表达影响总生存期。10年总生存率仅为30%。

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Vascular endothelial growth factor receptor 2 as a marker for malignant vascular tumors and mesothelioma: an immunohistochemical study of 262 vascular endothelial and 1640 nonvascular tumors.血管内皮生长因子受体 2 作为恶性血管肿瘤和间皮瘤的标志物:262 例血管内皮肿瘤和 1640 例非血管肿瘤的免疫组化研究。
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