{"title":"Can vascular endothelial growth factor C expression be of use in predicting surgical stage or prognosis in vulvar cancer","authors":"R. Nyberg, Marita Laurila, S. Staff, J. Mäenpää","doi":"10.14312/2052-4994.2017-10","DOIUrl":null,"url":null,"abstract":"Introduction: Nodal metastasis is a main prognostic factor in vulvar cancer. Increased vascular endothelial growth factor C (VEGF-C) expression has been associated with lymph node metastasis and poor prognosis in many cancers. The aim of this retrospective study was to investigate VEGF-C expression pattern in the invasive edge of vulvar cancer and in sentinel lymph node metastasis, and its association with the stage and prognosis. Methods: Tumor and sentinel lymph node samples from 44 patients were evaluated with immunohistochemistry, and the results were linked with the clinicopathological data. Results: Sixty-seven percent of primary tumors and 76% of sentinel lymph node metastases expressed VEFG-C. Positive VEGF-C expression of the primary tumor did not predict surgical Stage or sentinel lymph node involvement. The risk of relapse was not significantly higher with VEGF-C expressing tumors than with VEGF-C negative tumors (RR 2.55, 95% CI 0.66-9.90, p = 0.18). The risk of groin recurrence was significantly lower with VEGF-C positive than negative tumors (RR 0.36, 95% CI 0.16-0.79, p = 0.01). Survival was similar in both groups. No non-sentinel lymph node metastases were found in case of negative VEGF-C expression in the sentinel lymph node metastasis, whereas with positive VEGF-C expression they were found in 5/13 (38%) of cases. Conclusions: Tumoral VEGF-C expression was not associated with higher surgical Stage or poorer prognosis in vulvar cancer. However, absence of its expression in sentinel lymph node metastasis might indicate a low risk for non-sentinel lymph node metastases.","PeriodicalId":90205,"journal":{"name":"Journal of cancer research & therapy","volume":"66 1","pages":"50-55"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cancer research & therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14312/2052-4994.2017-10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Nodal metastasis is a main prognostic factor in vulvar cancer. Increased vascular endothelial growth factor C (VEGF-C) expression has been associated with lymph node metastasis and poor prognosis in many cancers. The aim of this retrospective study was to investigate VEGF-C expression pattern in the invasive edge of vulvar cancer and in sentinel lymph node metastasis, and its association with the stage and prognosis. Methods: Tumor and sentinel lymph node samples from 44 patients were evaluated with immunohistochemistry, and the results were linked with the clinicopathological data. Results: Sixty-seven percent of primary tumors and 76% of sentinel lymph node metastases expressed VEFG-C. Positive VEGF-C expression of the primary tumor did not predict surgical Stage or sentinel lymph node involvement. The risk of relapse was not significantly higher with VEGF-C expressing tumors than with VEGF-C negative tumors (RR 2.55, 95% CI 0.66-9.90, p = 0.18). The risk of groin recurrence was significantly lower with VEGF-C positive than negative tumors (RR 0.36, 95% CI 0.16-0.79, p = 0.01). Survival was similar in both groups. No non-sentinel lymph node metastases were found in case of negative VEGF-C expression in the sentinel lymph node metastasis, whereas with positive VEGF-C expression they were found in 5/13 (38%) of cases. Conclusions: Tumoral VEGF-C expression was not associated with higher surgical Stage or poorer prognosis in vulvar cancer. However, absence of its expression in sentinel lymph node metastasis might indicate a low risk for non-sentinel lymph node metastases.
结转移是外阴癌的主要预后因素。在许多癌症中,血管内皮生长因子C (VEGF-C)表达升高与淋巴结转移和预后不良有关。本回顾性研究旨在探讨VEGF-C在外阴癌侵袭边缘和前哨淋巴结转移中的表达模式及其与分期和预后的关系。方法:对44例患者的肿瘤和前哨淋巴结标本进行免疫组化评价,并将结果与临床病理资料相结合。结果:67%的原发肿瘤和76%的前哨淋巴结转移表达VEFG-C。原发肿瘤VEGF-C阳性表达不能预测手术分期或前哨淋巴结受累。VEGF-C表达肿瘤的复发风险不高于VEGF-C阴性肿瘤(RR 2.55, 95% CI 0.66-9.90, p = 0.18)。VEGF-C阳性肿瘤腹股沟复发风险明显低于阴性肿瘤(RR 0.36, 95% CI 0.16-0.79, p = 0.01)。两组的生存率相似。前哨淋巴结转移中VEGF-C表达阴性者未发现非前哨淋巴结转移,而VEGF-C表达阳性者有5/13(38%)发现非前哨淋巴结转移。结论:肿瘤VEGF-C表达与外阴癌手术分期高或预后差无关。然而,在前哨淋巴结转移中缺乏表达可能表明非前哨淋巴结转移的风险较低。