Single versus multiple primary melanomas

被引:48
作者
Hwa, Charlotte [1 ]
Price, Leah S. [2 ]
Belitskaya-Levy, Ilana [2 ,3 ,4 ]
Ma, Michelle W. [1 ,3 ]
Shapiro, Richard L. [3 ,5 ,6 ]
Berman, Russell S. [3 ,5 ,6 ]
Kamino, Hideko [3 ,7 ]
Darvishian, Farbod [3 ,7 ]
Osman, Iman [1 ,3 ,6 ]
Stein, Jennifer A. [1 ,3 ]
机构
[1] NYU, Sch Med, Ronald O Perelman Dept Dermatol, New York, NY 10016 USA
[2] NYU, Sch Med, Div Biostat, New York, NY 10016 USA
[3] NYU, Sch Med, Interdisciplinary Melanoma Cooperat Grp, New York, NY 10016 USA
[4] Vet Hlth Adm, Palo Alto Coordinating Ctr, Cooperat Studies Program, Palo Alto, CA USA
[5] NYU, Sch Med, Dept Surg, New York, NY 10016 USA
[6] NYU, Inst Canc, New York, NY 10016 USA
[7] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
关键词
melanoma; second primary; mitosis; early diagnosis; skin neoplasms; PRIMARY CUTANEOUS MELANOMA; 2ND PRIMARY MELANOMA; TUMOR MITOTIC RATE; RISK-FACTORS; FOLLOW-UP; PROGNOSTIC IMPORTANCE; MALIGNANT-MELANOMA; CDKN2A MUTATIONS; NEVI; ASSOCIATION;
D O I
10.1002/cncr.27407
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In patients with multiple primary melanomas (MPM), mean tumor thickness tends to decrease from the first melanoma to the second melanoma, and prognosis may be improved compared with the prognosis for patients who have a single primary melanoma (SPM). In this study, the authors compared the clinicopathologic features of patients with MPM and SPM to better characterize the differences between these 2 groups and to determine whether or not there is an inherent difference in tumor aggression. METHODS: In total, 788 patients with melanoma who were enrolled prospectively in the Interdisciplinary Melanoma Cooperative Group database from 2002 to 2008 were studied. Patients with SPM and with MPM were compared with regard to clinical and primary melanoma characteristics. RESULTS: Of 788 patients with melanoma, 61 patients (7.7%) had 2 or more primary melanomas. The incidence of developing a second primary melanoma 1 year and 5 years after initial melanoma diagnosis was 4.1% and 8.7%, respectively, and most of the risk accumulated within the first year. The incidence of MPM was greater in patients aged =60 years than in those aged =60 years. The absence or presence of mitosis and other tumor characteristics did not differ significantly between patients with SPM and patients with MPM (P = .61). CONCLUSIONS: No difference was observed in the presence or absence of mitoses, a marker of tumor proliferation, in SPM and MPM. Because it has been demonstrated that the presence of mitosis is a powerful prognostic marker, the current findings suggested that the tumors behave similarly in patients with SPM and patients with MPM. The authors concluded that differences in tumor thickness and prognosis between SPM and MPM more likely are caused by factors other than tumor biology, such as increased surveillance. Cancer 2012. (c) 2012 American Cancer Society.
引用
收藏
页码:4184 / 4192
页数:9
相关论文
共 53 条
[1]  
American Cancer Society, 2011, WHAT AR KEY STAT MEL
[2]  
[Anonymous], 2010, Cancer Facts Figures 2010
[3]   MULTIPLE PRIMARY MELANOMAS - DATA AND SIGNIFICANCE [J].
ARIYAN, S ;
POO, WJ ;
BOLOGNIA, J ;
BUZAID, A ;
ARIYAN, T .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1995, 96 (06) :1384-1389
[4]   Tumor mitotic rate is a more powerful prognostic indicator than ulceration in patients with primary cutaneous melanoma - An analysis of 3661 patients from a single center [J].
Azzola, MF ;
Shaw, HM ;
Thompson, JF ;
Soong, SJ ;
Scolyer, RA ;
Watson, GF ;
Colman, MH ;
Zhang, YT .
CANCER, 2003, 97 (06) :1488-1498
[5]   Final Version of 2009 AJCC Melanoma Staging and Classification [J].
Balch, Charles M. ;
Gershenwald, Jeffrey E. ;
Soong, Seng-jaw ;
Thompson, John F. ;
Atkins, Michael B. ;
Byrd, David R. ;
Buzaid, Antonio C. ;
Cochran, Alistair J. ;
Coit, Daniel G. ;
Ding, Shouluan ;
Eggermont, Alexander M. ;
Flaherty, Keith T. ;
Gimotty, Phyllis A. ;
Kirkwood, John M. ;
McMasters, Kelly M. ;
Mihm, Martin C., Jr. ;
Morton, Donald L. ;
Ross, Merrick I. ;
Sober, Arthur J. ;
Sondak, Vernon K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6199-6206
[6]   The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma:: An international population-based study [J].
Berwick, Marianne ;
Orlow, Irene ;
Hummer, Amanda J. ;
Armstrong, Bruce K. ;
Kricker, Anne ;
Marrett, Loraine D. ;
Millikan, Robert C. ;
Gruber, Stephen B. ;
Anton-Culver, Hoda ;
Zanetti, Roberto ;
Gallagher, Richard P. ;
Dwyer, Terence ;
Rebbeck, Timothy R. ;
Kanetsky, Peter A. ;
Busam, Klaus ;
From, Lynn ;
Mujumdar, Urvi ;
Wilcox, Homer ;
Begg, Colin B. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (08) :1520-1525
[7]   Really synchronous cutaneous melanomas: serendipity or need for prevention? [J].
Betti, Roberto ;
Gualandri, Lorenzo ;
Vergani, Raffaella ;
Menni, Silvano ;
Crosti, Carlo .
EUROPEAN JOURNAL OF DERMATOLOGY, 2009, 19 (03) :258-259
[8]   Multiple primary melanoma revisited [J].
Blackwood, MA ;
Holmes, R ;
Synnestvedt, M ;
Young, M ;
George, G ;
Yang, H ;
Elder, DE ;
Schuchter, LM ;
Guerry, D ;
Ganguly, A .
CANCER, 2002, 94 (08) :2248-2255
[9]   Multiple primary melanomas: Implications for screening and follow-up programs for melanoma [J].
Brobeil, A ;
Rapaport, D ;
Wells, K ;
Cruse, CW ;
Glass, F ;
Fenske, N ;
Albertini, J ;
Miliotis, G ;
Messina, J ;
DeConti, R ;
Berman, C ;
Shons, A ;
Cantor, A ;
Reintgen, DS .
ANNALS OF SURGICAL ONCOLOGY, 1997, 4 (01) :19-23
[10]  
BURDEN AD, 1994, BRIT MED J, V309, P375