Sentinel lymph node biopsy and melanoma biology

被引:14
作者
Essner, R
机构
[1] John Wayne Canc Inst, Dept Surg Oncol, Santa Monica, CA 90404 USA
[2] John Wayne Canc Inst, Dept Mol Therapeut, Santa Monica, CA 90404 USA
关键词
D O I
10.1158/1078-0432.CCR-05-2506
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Minimally invasive intraoperative lymphatic mapping and sentinel node biopsy has become the standard approach for staging the regional lymph nodes for early-stage melanoma The procedure requires close collaboration of surgeon, pathologist, and nuclear medicine physician. The strength of lymphatic mapping and sentinel node biopsy is its accuracy of detecting occult lymph node metastases. Reverse transcriptase-PCR (RT-PCR) analyses of either fresh-frozen or paraffin-embedded sections of the sentinel lymph nodes have been found to be more sensitive than H&E staining or immunohistochemistry techniques, but lack of specificity and limits in the availability of tissue specimens make this technique impractical for routine use. Three randomized clinical trials are examining the therapeutic value of lymphatic mapping and sentinel node biopsy for melanoma. Preliminary results of the Multicenter Lymphadenectomy Trial I show the high level of accuracy and low morbidity of lymphatic mapping and sentinel node biopsy done through an international working group The therapeutic value of lymphatic mapping and sentinel node biopsy is still unclear. Multicenter Lymphadenectomy Trial 11 will test the clinical significance of lymph nodes evaluated by RT-PCR and the value of completion lymph node dissection for patients found to have tumor-positive sentinel lymph nodes by H&E, immunohistochemistry, or RT-PCR. The Sunbelt Melanoma Trial examines the therapeutic value of completion dissection and benefits of Intron A. The ability to detect occult nodal metastases and evaluate the interaction of primary tumor with the regional lymph nodes may provide for better understanding of the metastatic process in patients with melanoma and help to determine the function of the regional lymph nodes as markers of metastases or incubators of tumor cells in the metastatic cascade.
引用
收藏
页码:2320S / 2325S
页数:6
相关论文
共 17 条
[1]  
Alitalo Kari, 2004, Cancer Res, V64, P9225, DOI 10.1158/0008-5472.CAN-04-2475
[2]   Immediate or delayed dissection of regional nodes in patients with melanoma of the trunk: a randomised trial [J].
Cascinelli, N ;
Morabito, A ;
Santinami, M ;
MacKie, RM ;
Belli, F .
LANCET, 1998, 351 (9105) :793-796
[3]   Update on lymphatic mapping and sentinel node biopsy in the management of patients with melanocytic tumours [J].
Cochran, AJ ;
Roberts, A ;
Wen, DR ;
Huang, RR ;
Itakura, E ;
Luo, F ;
Binder, SW .
PATHOLOGY, 2004, 36 (05) :478-484
[4]   Sentinel lymph nodes show profound downregulation of antigen-presenting cells of the paracortex: Implications for tumor biology and treatment [J].
Cochran, AJ ;
Morton, DL ;
Stern, S ;
Lana, AMA ;
Essner, R ;
Wen, DR .
MODERN PATHOLOGY, 2001, 14 (06) :604-608
[5]  
Essner R, 2002, ONCOLOGY-NY, V16, P27
[6]   Standardized probe-directed sentinel node dissection in melanoma [J].
Essner, R ;
Bostick, PJ ;
Glass, EC ;
Foshag, LJ ;
Haigh, PI ;
Wang, HJ ;
Morton, DL .
SURGERY, 2000, 127 (01) :26-31
[7]   Efficacy of lymphatic mapping, sentinel lymphadenectomy, and selective complete lymph node dissection as a therapeutic procedure for early-stage melanoma [J].
Essner, R ;
Conforti, A ;
Kelley, MC ;
Wanek, L ;
Stern, S ;
Glass, E ;
Morton, DL .
ANNALS OF SURGICAL ONCOLOGY, 1999, 6 (05) :442-449
[8]   Patterns of recurrence following a negative sentinel lymph node biopsy in 243 patients with stage I or II melanoma [J].
Gershenwald, JE ;
Colome, MI ;
Lee, JE ;
Mansfield, PF ;
Tseng, CH ;
Lee, JJ ;
Balch, CM ;
Ross, MI .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (06) :2253-2260
[9]  
Lee JH, 2005, CLIN CANCER RES, V11, P107
[10]   Factors predictive of tumor-positive nonsentinel lymph nodes after tumor-positive sentinel lymph node dissection for melanoma [J].
Lee, JH ;
Essner, R ;
Torisu-Itakura, H ;
Wanek, L ;
Wang, HJ ;
Morton, DL .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (18) :3677-3684