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非典型低血管化骨肉瘤患者的生存率提高。

Improved survival in osteosarcoma patients with atypical low vascularization.

作者信息

Kunz Pierre, Fellenberg Joerg, Moskovszky Linda, Sápi Zoltan, Krenacs Tibor, Machado Isidro, Poeschl Johannes, Lehner Burkhard, Szendrõi Miklos, Ruef Peter, Bohlmann Michael, Bosch Antonio Llombart, Ewerbeck Volker, Kinscherf Ralf, Fritzsching Benedikt

机构信息

Department of Orthopedics and Traumatology, University Hospital Heidelberg, Heidelberg, Germany,

出版信息

Ann Surg Oncol. 2015 Feb;22(2):489-96. doi: 10.1245/s10434-014-4001-2. Epub 2014 Aug 26.

Abstract

BACKGROUND

Osteosarcoma is considered a highly vascularized bone tumor with early metastatic dissemination through intratumoral blood vessels mostly into the lung. Novel targets for therapy such as tumor vascularization are highly warranted since little progress has been achieved in the last 30 years. However, proof of relevance for vascularization as a major prognostic parameter has been hampered by tumor heterogeneity, difficulty in detecting microvessels by immunohistochemistry, and small study cohorts. Most recently, we demonstrated that highly standardized whole-slide imaging could overcome these limitations (Kunz et al., PloS One 9(3):e90727, 2014). In this study, we applied this method to a multicenter cohort of 131 osteosarcoma patients to test osteosarcoma vascularization as a prognostic determinant.

METHODS

Computer-assisted whole-slide analysis, together with enzymatic epitope retrieval, was used for CD31-based microvessel quantification in 131 pretreatment formalin-fixed and paraffin-embedded biopsies from three bone tumor centers. Kaplan-Meier-estimated survival and chemoresponse were determined and multivariate analysis was performed. Conventional hot-spot-based microvessel density (MVD) determination was compared with whole-slide imaging.

RESULTS

We detected high estimated overall (p ≤ 0.008) and relapse-free (p ≤ 0.004) survival in 25 % of osteosarcoma patients with low osteosarcoma vascularization in contrast to other patient groups. Furthermore, all patients with low osteosarcoma vascularization showed a good response to neoadjuvant chemotherapy. Comparison of conventional MVD determination with whole-slide imaging suggests false high quantification or even exclusion of samples with low osteosarcoma vascularization due to difficult CD31 detection in previous studies.

CONCLUSION

Low intratumoral vascularization at the time of diagnosis is a strong predictor for prolonged survival and good response to neoadjuvant chemotherapy in osteosarcoma.

摘要

背景

骨肉瘤被认为是一种血管高度丰富的骨肿瘤,早期可通过肿瘤内血管发生转移,主要转移至肺部。由于在过去30年里进展甚微,因此迫切需要新的治疗靶点,如肿瘤血管生成。然而,肿瘤异质性、免疫组织化学检测微血管的困难以及研究队列较小,阻碍了血管生成作为主要预后参数的相关性验证。最近,我们证明了高度标准化的全切片成像可以克服这些局限性(Kunz等人,《公共科学图书馆·综合》9(3):e90727,2014年)。在本研究中,我们将此方法应用于一个由131名骨肉瘤患者组成的多中心队列,以测试骨肉瘤血管生成作为预后决定因素。

方法

采用计算机辅助全切片分析,并结合酶促抗原修复,对来自三个骨肿瘤中心的131份预处理福尔马林固定石蜡包埋活检组织进行基于CD31的微血管定量分析。确定Kaplan-Meier估计生存率和化疗反应,并进行多变量分析。将基于传统热点的微血管密度(MVD)测定结果与全切片成像结果进行比较。

结果

与其他患者组相比,我们发现25%骨肉瘤血管生成低的骨肉瘤患者的总体生存率(p≤0.008)和无复发生存率(p≤0.004)估计值较高。此外,所有骨肉瘤血管生成低的患者对新辅助化疗均表现出良好反应。传统MVD测定结果与全切片成像结果的比较表明,由于以往研究中CD31检测困难,可能会出现微血管定量错误偏高,甚至排除骨肉瘤血管生成低的样本。

结论

诊断时肿瘤内血管生成低是骨肉瘤患者生存期延长和对新辅助化疗反应良好的有力预测指标。

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