Minimum Safe Pathologic Excision Margins for Primary Cutaneous Melanomas (1-2 mm in Thickness): Analysis of 2131 Patients Treated at a Single Center

被引:25
作者
Haydu, Lauren E. [1 ,2 ]
Stollman, Joram T. [1 ]
Scolyer, Richard A. [1 ,3 ,4 ]
Spillane, Andrew J. [1 ,2 ]
Quinn, Michael J. [1 ,2 ]
Saw, Robyn P. M. [1 ,2 ]
Shannon, Kerwin F. [1 ,2 ]
Stretch, Jonathan R. [1 ,2 ]
Bonenkamp, Johannes J. [5 ]
Thompson, John F. [1 ,2 ]
机构
[1] Melanoma Inst Australia, North Sydney, NSW, Australia
[2] Univ Sydney, Discipline Surg, Sydney Med Sch, Sydney, NSW 2006, Australia
[3] Univ Sydney, Discipline Pathol, Sydney Med Sch, Sydney, NSW 2006, Australia
[4] Royal Prince Alfred Hosp, Tissue Pathol & Diagnost Oncol, Sydney, NSW, Australia
[5] Radboud Univ Nijmegen, Med Ctr, Dept Surg, NL-6525 ED Nijmegen, Netherlands
关键词
2; CM; SURGICAL MARGINS; NODE BIOPSY; RECURRENCE; RESECTION; 2-CM;
D O I
10.1245/s10434-015-4575-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was designed to determine the minimum safe pathologic excision margin for primary cutaneous melanomas 1.01-2.00-mm thick (T2) and to identify prognostic factors that influence survival in these patients. Several studies have shown previously that "narrow" clinical excision margins (1-2 cm in vivo) are as safe as "wide" excision margins (4-5 cm) for management of primary T2 melanomas. However, pathologic margins are likely to be a better predictor of recurrence than clinical margins. Clinicopathologic and follow-up data for 2131 T2 melanoma patients treated at Melanoma Institute Australia between January 1992 and May 2012 were analyzed. Of the 2131 patients, those who had a pathologic excision margin of < 8 mm (equivalent to 1 cm in vivo) had poorer prognosis in terms of disease-free survival compared with the 8-16-mm group (equivalent to 1-2 cm in vivo; P = 0.044). When comparing 8-mm with 16-mm pathologic margins, no differences were observed in any of the survival outcomes. Only the deep margin proved to be an independent predictor of local and in-transit recurrence-free survival (P = 0.003) in all excision margin categories. Pathologic excision margins < 8 mm were associated with worse regional node recurrence-free survival and distant recurrence-free survival compared with margins a parts per thousand yen8 mm (P = 0.049 and P = 0.045; respectively). However, these results failed to translate into a statistically significant difference in melanoma-specific survival. The results of this study suggest that if a peripheral/radial pathologic excision margin for a T2 primary cutaneous melanoma is < 8 mm consideration should be given to performing a wider excision.
引用
收藏
页码:1071 / 1081
页数:11
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