Incidence of sentinel node metastasis in patients with thin primary melanoma (≤1 mm) with vertical growth phase

被引:138
作者
Bedrosian, I
Faries, MB
Guerry, D
Elenitsas, R
Schuchter, L
Mick, R
Spitz, FR
Bucky, LP
Alavi, A
Elder, DE
Fraker, DL
Czerniecki, BJ
机构
[1] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Dermatol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Surg, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[7] Univ Penn, Ctr Canc, Philadelphia, PA 19104 USA
[8] Univ Penn, Pigmented Les Grp, Philadelphia, PA 19104 USA
关键词
vertical growth phase; thin melanoma; sentinel node; metastasis;
D O I
10.1007/s10434-000-0262-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Patients with thin primary melanomas (less than or equal to 1 mm) generally have an excellent prognosis. However, the presence of a vertical growth phase (VGP) adversely impacts the survival rate. We report on the rate of occurrence of nodal metastasis in patients with thin primary melanomas with a VGP who are offered sentinel lymph node (SLN) biopsy. Methods: Among 235 patients with clinically localized cutaneous melanomas who underwent successful SLN biopsy, 71 had lesions 1 mm or smaller with a VGP. The SLN was localized by using blue dye and a radiotracer. If negative for tumor by using hematoxylin and eosin staining, the SLN was further examined by immunohistochemistry. Results: The rate of occurrence of SLN metastasis was 15.2% in patients with melanomas deeper than 1 mm and 5.6% in patients with thin melanomas. Three patients with thin melanomas and a positive SLN had low-risk lesions, based on a highly accurate six-variable multivariate logistic regression model for predicting 8-year survival in stage I/II melanomas. The fourth patient had a low- to intermediate-risk lesion based on this model. At the time of the lymphadenectomy, one patient had two additional nodes with metastasis. Conclusions: VGP in a melanoma 1 mm or smaller seems to be a risk factor for nodal metastasis. The risk of nodal disease may not be accurately predicted by the use of a multivariate logistic regression model that incorporates thickness, mitotic rate, regression, tumor-infiltrating lymphocytes, sex, and anatomical site. Patients with thin lesions having VGP should be evaluated for SLN biopsy and trials of adjuvant therapy when stage III disease is found.
引用
收藏
页码:262 / 267
页数:6
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