Improved survival after lymphadenectomy for nodal metastasis from an unknown primary melanoma

被引:85
作者
Lee, Chris C.
Faries, Mark B.
Wanek, Leslie A.
Morton, Donald L. [1 ]
机构
[1] St Johns Hlth Ctr, John Wayne Canc Inst, Roy E Coats Res Labs, Santa Monica, CA 90404 USA
关键词
D O I
10.1200/JCO.2007.14.0285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose No primary lesion is identified in 10% to 20% of patients presenting with palpable evidence of regional metastatic melanoma. Because the prognostic significance of unknown primary melanoma ( MUP) is unclear, we compared clinical outcomes of patients with MUP and known primary melanoma ( MKP) with regional nodal metastases. Patients and Methods We reviewed our 13,000-patient prospective melanoma database ( 1971 through 2005) to identify patients managed with regional lymphadenectomy for palpable nodal metastases from MUP or MKP. Multivariate analysis identified prognostic factors significant for survival. MUP and MKP were then matched by significant covariates. Overall survival ( OS) was estimated by Kaplan-Meier method and compared by log-rank analysis. Results Multivariate analysis of data from 1,571 study patients identified four significant covariates associated with worse prognosis: age >= 60 years ( hazard ratio [ HR] = 1.294; P =.0017), male sex ( HR = 1.335; P =.0004), nodal tumor burden >= one ( HR = 1.256; P <.0001), and known primary ( HR = 1.507; 95% CI, 1.220 to 1.862; P =.0001). Five-year OS was significantly higher for 262 patients with MUP than for 1,309 patients with MKP ( 55% +/- 6% v 44% +/- 3%; P =.0021). Computerized matching of MUP and MKP by four significant covariates ( age, sex, nodal tumor burden, and decade of diagnosis) yielded 221 matched pairs. Median and 5-year OS rates were 165 months and 58% +/- 7%, respectively, for MUP as compared with 34 months and 40% +/- 7%, respectively, for MKP ( P =.0006). Conclusion Lymphadenectomy is effective for nodal metastasis from MUP. The significantly better postoperative survival for MUP versus MKP suggests a strong endogenous immune response against the primary melanoma. Immunologic studies to identify cell-mediated and antibody components of this response may lead to new approaches for determining melanoma prognosis and treatment.
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页码:535 / 541
页数:7
相关论文
共 39 条
[1]  
Anbari KK, 1997, CANCER-AM CANCER SOC, V79, P1816, DOI 10.1002/(SICI)1097-0142(19970501)79:9<1816::AID-CNCR26>3.0.CO
[2]  
2-#
[3]  
BAAB GH, 1975, ARCH SURG-CHICAGO, V110, P896
[4]   HISTOLOGICAL REGRESSION IN PRIMARY CUTANEOUS MELANOMA - RECOGNITION, PREVALENCE AND SIGNIFICANCE [J].
BLESSING, K ;
MCLAREN, KM .
HISTOPATHOLOGY, 1992, 20 (04) :315-322
[5]  
BODURTHA AJ, 1975, CANCER RES, V35, P189
[6]   HUMORAL CYTOTOXICITY IN MELANOMA PATIENTS AND ITS CORRELATION WITH EXTENT AND COURSE OF DISEASE [J].
CANEVARI, S ;
FOSSATI, G ;
DELLAPORTA, G ;
BALZARINI, GP .
INTERNATIONAL JOURNAL OF CANCER, 1975, 16 (05) :722-729
[7]  
Chang AE, 1998, CANCER, V83, P1664, DOI 10.1002/(SICI)1097-0142(19981015)83:8<1664::AID-CNCR23>3.0.CO
[8]  
2-G
[9]  
CHANG P, 1982, CANCER-AM CANCER SOC, V49, P1106, DOI 10.1002/1097-0142(19820315)49:6<1106::AID-CNCR2820490607>3.0.CO
[10]  
2-0