Tabone Marie-Dominique, Brugières Laurence, Piperno-Neumann Sophie, Selva Marie-Ange, Marec-Bérard Perrine, Pacquement Hélène, Lervat Cyril, Corradini Nadège, Gentet Jean-Claude, Couderc Rémy, Chevance Aurélie, Mahier-Ait Oukhatar Céline, Entz-Werle Natacha, Blay Jean-Yves, Le Deley Marie-Cecile
Department of Paediatric Onco-Haematology, Armand Trousseau Hospital, 26 avenue du Dr A. Netter, 75571, Paris cedex12, France.
Department of Paediatric Onco-Haematology AP-HP, GHUEP, Trousseau La Roche-Guyon Hospital, 26 avenue du Dr A. Netter, 75012, Paris, France.
BMC Cancer. 2017 Jun 15;17(1):419. doi: 10.1186/s12885-017-3409-z.
Angiogenesis is essential for the progression and metastatic spread of solid tumours. Expression of vascular endothelial growth factor (VEGF) has been linked to poor survival among osteosarcoma patients but the clinical relevance of monitoring blood and urine angiogenic factors is uncertain. The aim of this study was to determine the prognostic significance of blood VEGF and blood and urinary basic fibroblast growth factor (bFGF) levels in osteosarcoma patients, both at diagnosis and during treatment.
Patients with localised or metastatic osteosarcoma enrolled in OS2005 and OS2006 studies between 2005 and 2011 were prospectively included in this study. VEGF and bFGF levels in serum and plasma and bFGF levels in urine were measured by ELISA at diagnosis, before surgery, and at the end of treatment. Endpoints considered for the prognostic analysis were histological response, progression-free and overall survival. Kruskal-Wallis tests were used to compare the distribution of baseline biomarker values across the different subgroups, and paired sample Wilcoxon rank tests were used to analyze changes over time. Association between biomarker levels and outcomes were assessed in multivariable models (logistic regression for histologic response, and Cox models for survival).
Samples were available at diagnosis for 269 patients (54% males; age ≤ 18 years: 73%; localised disease in 68%, doubtful lung lesions in 17%, and metastases in 15%). High serum VEGF and bFGF levels were observed in respectively 61% and 51% of patients. Serum and plasma VEGF values were not strongly correlated with one another (r = 0.53). High serum and plasma VEGF levels were significantly more frequent in patients with large tumours (≥10 cm; p = 0.003 and p = 0.02, respectively). VEGF levels fell significantly during pre-operative chemotherapy (p < 0.0001). No significant correlation was found between this variation and either the histological response, progression-free survival or overall survival (p = 0.26, p = 0.67, and p = 0.87, respectively). No significant association was found between blood or urinary bFGF levels and clinical characteristics, histological response, or survival.
Levels of VEGF and bFGF angiogenic factors are high in most osteosarcoma patients, but have no significant impact on response to chemotherapy or outcome in this large prospective series. OS 2006 TRIAL REGISTRATION NUMBER: clinicaltrials.gov NCT00470223; date of registration: May 3th 2007.
血管生成对于实体瘤的进展和转移扩散至关重要。血管内皮生长因子(VEGF)的表达与骨肉瘤患者的不良生存相关,但监测血液和尿液血管生成因子的临床相关性尚不确定。本研究的目的是确定骨肉瘤患者在诊断时和治疗期间血液VEGF以及血液和尿液碱性成纤维细胞生长因子(bFGF)水平的预后意义。
2005年至2011年参加OS2005和OS2006研究的局限性或转移性骨肉瘤患者被前瞻性纳入本研究。在诊断时、手术前和治疗结束时通过酶联免疫吸附测定(ELISA)测量血清和血浆中的VEGF和bFGF水平以及尿液中的bFGF水平。预后分析考虑的终点是组织学反应、无进展生存期和总生存期。使用Kruskal-Wallis检验比较不同亚组中基线生物标志物值的分布,并使用配对样本Wilcoxon秩和检验分析随时间的变化。在多变量模型中评估生物标志物水平与结局之间的关联(组织学反应采用逻辑回归,生存期采用Cox模型)。
269例患者在诊断时有样本可用(54%为男性;年龄≤18岁:73%;局限性疾病68%,可疑肺部病变17%,转移15%)。分别在61%和51%的患者中观察到高血清VEGF和bFGF水平。血清和血浆VEGF值彼此之间相关性不强(r = 0.53)。大肿瘤(≥10 cm)患者中高血清和血浆VEGF水平明显更常见(分别为p = 0.003和p = 0.02)。术前化疗期间VEGF水平显著下降(p < 0.0001)。未发现这种变化与组织学反应、无进展生存期或总生存期之间存在显著相关性(分别为p = 0.26、p = 0.67和p = 0.87)。未发现血液或尿液bFGF水平与临床特征、组织学反应或生存期之间存在显著关联。
大多数骨肉瘤患者的VEGF和bFGF血管生成因子水平较高,但在这个大型前瞻性系列研究中对化疗反应或结局没有显著影响。OS 2006试验注册号:clinicaltrials.gov NCT00470223;注册日期:2007年5月3日。