Nyström H, Jönsson M, Werner-Hartman L, Nilbert M, Carneiro A
Lund University, Skåne University Hospital, Department of Clinical Sciences Lund, Oncology, Lund, Sweden.
Lund University, Faculty of Medicine, Department of Clinical Sciences Lund, Oncology, Lund, Sweden.
J Clin Pathol. 2017 Oct;70(10):879-885. doi: 10.1136/jclinpath-2016-204149. Epub 2017 Apr 12.
Sarcomas are of mesenchymal origin and typically show abundant tumour stroma and presence of necrosis. In search for novel biomarkers for personalised therapy, we determined the prognostic impact of stromal markers, hypoxia and neovascularity in high-grade soft tissue leiomyosarcoma and pleomorphic undifferentiated sarcoma.
We evaluated CD163, colony-stimulating factor (CSF)-1, CD16 and hypoxia-inducible factor 1 (HIF-1)α using immunohistochemical staining and assessed microvessel density using CD31 in 73 high-grade leiomyosarcomas and undifferentiated pleomorphic sarcomas of the extremities and the trunk wall. The results were correlated to metastasis-free and overall survival.
Expression of HIF-1α was associated with the presence of necrosis and independently predicted shorter metastasis-free survival (HR 3.2, CI 1.4 to 7.0, p=0.004), whereas neither expression of the stromal markers CD163, CD16 and CSF-1 nor microvessel density was prognostically relevant in this series.
There is increasing evidence for the prognostic role of hypoxia in high-grade soft tissue sarcoma, and these data suggest that HIF-1α expression represents a candidate prognostic biomarker for clinical application in high-grade leiomyosarcoma and undifferentiated pleomorphic sarcoma.
肉瘤起源于间充质,通常表现为丰富的肿瘤间质和坏死灶。为寻找用于个体化治疗的新型生物标志物,我们确定了基质标志物、缺氧和新生血管在高级别软组织平滑肌肉瘤和多形性未分化肉瘤中的预后影响。
我们采用免疫组织化学染色评估了73例四肢和躯干壁高级别平滑肌肉瘤及未分化多形性肉瘤中的CD163、集落刺激因子(CSF)-1、CD16和缺氧诱导因子1(HIF-1)α,并使用CD31评估微血管密度。结果与无转移生存期和总生存期相关。
HIF-1α的表达与坏死的存在相关,并独立预测较短的无转移生存期(HR 3.2,CI 1.4至7.0,p = 0.004),而在本系列中,基质标志物CD163、CD16和CSF-1的表达以及微血管密度均与预后无关。
越来越多的证据表明缺氧在高级别软组织肉瘤中具有预后作用,这些数据表明HIF-1α表达代表了一种可用于高级别平滑肌肉瘤和未分化多形性肉瘤临床应用的候选预后生物标志物。