VEGF expression as a prognostic marker in osteosarcoma

医学 骨肉瘤 血管内皮生长因子 分级(工程) 免疫组织化学 病理 血管生成 一致性 活检 坏死 血管内皮生长因子A 肿瘤科 化疗 内科学 血管内皮生长因子受体 生物 生态学
作者
Jyoti Bajpai,Meharchand C. Sharma,Vishnubhatla Sreenivas,Rajesh Kumar,Shivanand Gamnagatti,Shah Alam Khan,Shishir Rastogi,Arun Malhotra,Sameer Bakhshi
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:53 (6): 1035-1039 被引量:54
标识
DOI:10.1002/pbc.22178
摘要

The vascular endothelial growth factor (VEGF) pathway is the key regulator of angiogenesis. In osteosarcoma baseline VEGF is of proven prognostic value but prognostic potential of post-NACT VEGF expression is largely unexplored.Treatment naive patients with osteosarcoma were subjected to initial staging workup followed by three cycles of neoadjuvant chemotherapy (NACT) and surgery; resected tumors were assessed for histological necrosis by Huvos grading. Initial biopsy and resected tumor specimens post-NACT were examined for VEGF expression by immunohistochemistry. Positive VEGF expression was considered when intensive positive staining was observed in >10% of the tumor cells. VEGF expression at baseline was compared with grade of tumor; pre-NACT and post-NACT VEGF expression were compared with histological necrosis. Receiver operating characteristic curves were generated to assess best threshold and predictability.A total of 31 patients were recruited with median age of 17 years (range 5-66 years); male/female ratio was 25:6; 23 patients (74%) were non-metastatic. At baseline, there was 90% concordance between positive VEGF expression and higher histological grade (28/31); baseline VEGF expression did not correlate well with stage and histological necrosis. Twenty-one (67%) were poor and 10 (33%) were good histologic responders; post-NACT VEGF expression as well as VEGF change following NACT significantly correlated with histological necrosis.Positive VEGF expression in surviving tumor cells post-NACT in resected tumors appears to be an important negative prognostic factor in osteosarcoma which may help future therapies to be identified according to the angiogenic potential of the disease.

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