Lymphovascular Invasion as a Prognostic Factor in Melanoma

被引:0
作者
Egger, Michael E. [1 ]
Gilbert, Julianna E. [2 ]
Burton, Alison L. [2 ]
McMasters, Kelly M. [1 ]
Callender, Glenda G. [1 ]
Quillo, Amy R. [1 ]
Brown, Russell E. [1 ]
St. Hill, Charles R. [1 ]
Hagendoorn, Lee [3 ]
Martin, Robert C. G., II [1 ]
Stromberg, Arnold J. [4 ]
Scoggins, Charles R. [1 ]
机构
[1] Univ Louisville, Dept Surg, Louisville, KY 40202 USA
[2] Univ Louisville, Sch Med, Louisville, KY 40202 USA
[3] Advertek Inc, Louisville, KY USA
[4] Univ Kentucky, Dept Stat, Lexington, KY 40506 USA
关键词
LYMPH-NODE STATUS; CUTANEOUS MELANOMA; VASCULAR INVASION; YOUNGER AGE; STAGE-I; SENTINEL; PREDICT; POSITIVITY; BIOPSY; METASTASIS;
D O I
暂无
中图分类号
R61 [外科手术学];
学科分类号
摘要
The prognostic significance of lymphovascular invasion (LVI) in melanoma remains controversial. Clinicopathologic data from a prospective trial of patients with melanoma were analyzed with respect to LVI. Disease-free survival and overall survival (OS) were evaluated by Kaplan-Meier (KM) analysis. Univariate and multivariate analyses were performed to evaluate factors predictive of tumor-positive sentinel nodes (SLN) and survival. A total of 2183 patients were included in this analysis; 171 (7.8%) had LVI. Median follow-up was 68 months. Factors associated with LVI included tumor thickness, ulceration, and histologic subtype (P < 0.05). LVI was associated with a greater risk of SLN metastasis (P < 0.05). By KM analysis, LVI was associated with worse OS (P = 0.0009). On multivariate analysis, age, gender, thickness, ulceration, anatomic location, and SLN status were predictors of OS; however, LVI was not an independent predictor of OS. Among patients with regression, the 5-year OS rate was 49.4 per cent for patients with LVI versus 81.1 per cent for those with no LVI (P < 0.0001). LVI is associated with a greater risk of SLN metastasis. Although LVI is not an independent predictor of OS in general, it is a powerful predictor of worse OS among patients who have evidence of regression of the primary tumor.
引用
收藏
页码:992 / 997
页数:6
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