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The role of microvessel density lymph node metastasis and tumor size as prognostic factors of distant metastasis in colorectal cancer

机译:微血管密度淋巴结转移和肿瘤大小作为大肠癌远处转移预后因素的作用

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摘要

Angiogenesis is essential for tumor growth and metastasis. CD105 is reportedly a specific marker for tumor angiogenesis. It has been demonstrated that monoclonal antibodies to CD105 have high affinity for activated endothelial cells. A relationship between metastasis and microvessel density (MVD), as an indicator of neovascularization, has been identified in patients with colorectal cancer as shown by the presence of monoclonal antibodies to CD105. However, data on potentially confounding factors such as lymphatic and vascular infiltration and tumor size are lacking. We further investigated the relationship between MVD and distant metastasis, along with potentially confounding clinicopathological factors, to more precisely characterize this relationship. In this retrospective study, we analyzed colorectal cancer specimens surgically or endoscopically resected from January to September 2009. We defined MVD as the number of microvessels stained by monoclonal antibodies to CD105 per ×400 field. Selected clinicopathological factors were analyzed and stepwise multivariate logistic regression was performed to identify independent risk factors for distant metastasis. We analyzed 129 lesions. The median follow-up time was 34 months (range, 6–85 months) in patients with distant metastasis and 61 months (range, 60–86 months) in those without distant metastasis. At the time of resection or during subsequent follow-up, 32 patients had distant metastases. The MVD was significantly greater in patients with than without distant metastases (mean ± standard deviation: 10.4±4.9 vs. 7.6±3.3, P=0.008; Welch's t-test). Stepwise multivariate logistic regression indicated that MVD, regional lymph node metastasis, and tumor size were independent risk factors for distant metastases. Combining assessment of monoclonal antibodies to CD105-positive MVD with assessment of regional lymph node metastasis and tumor size may help to identify patients who need more intensive surveillance after surgery for colorectal cancer.
机译:血管生成对于肿瘤的生长和转移至关重要。据报道,CD105是肿瘤血管生成的特异性标记。已经证明,针对CD105的单克隆抗体对活化的内皮细胞具有高亲和力。如CD105单克隆抗体的存在所表明,在结直肠癌患者中已确定转移与微血管密度(MVD)之间的关系,作为新血管形成的指标。然而,缺乏关于潜在混淆因素如淋巴和血管浸润以及肿瘤大小的数据。我们进一步调查了MVD与远处转移之间的关系,以及可能混淆的临床病理因素,以更准确地表征这种关系。在这项回顾性研究中,我们分析了从2009年1月至2009年9月手术或内窥镜切除的结直肠癌标本。我们将MVD定义为每×400视野被CD105单克隆抗体染色的微血管数量。分析选定的临床病理因素,并进行逐步多元logistic回归分析,以确定远处转移的独立危险因素。我们分析了129个病变。有远处转移的患者中位随访时间为34个月(6-85个月),无远处转移的患者中位随访时间为61个月(60-86个月)。切除时或随后的随访中,有32例患者有远处转移。有远处转移的患者的MVD明显高于无远处转移的患者(平均值±标准差:10.4±4.9与7.6±3.3,P = 0.008; Welch's t检验)。逐步多因素logistic回归分析表明MVD,区域淋巴结转移和肿瘤大小是远处转移的独立危险因素。将针对CD105阳性MVD的单克隆抗体的评估与对区域淋巴结转移和肿瘤大小的评估相结合,可能有助于确定需要在大肠癌手术后进行更强化监护的患者。

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