Age as a Prognostic Factor in Patients with Localized Melanoma and Regional Metastases

被引:127
作者
Balch, Charles M. [1 ]
Soong, Seng-Jaw [2 ]
Gershenwald, Jeffrey E. [3 ]
Thompson, John F. [4 ]
Coit, Daniel G. [5 ]
Atkins, Michael B. [6 ]
Ding, Shouluan [7 ]
Cochran, Alistair J. [8 ,9 ]
Eggermont, Alexander M. M. [10 ]
Flaherty, Keith T. [11 ]
Gimotty, Phyllis A. [12 ]
Johnson, Timothy M. [13 ]
Kirkwood, John M. [14 ]
Leong, Stanley P. [15 ]
McMasters, Kelly M. [16 ]
Mihm, Martin C., Jr. [17 ]
Morton, Donald L. [18 ]
Ross, Merrick I. [3 ]
Sondak, Vernon K. [19 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Surg, Div Surg Oncol, Dallas, TX 75390 USA
[2] Univ Alabama Birmingham, Birmingham, AL USA
[3] UTMD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX USA
[4] Melanoma Inst Australia, Sydney, NSW, Australia
[5] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10021 USA
[6] MedStar Georgetown Univ Hosp, Lombardi Comprehens Canc Ctr, Washington, DC USA
[7] Univ Alabama Birmingham, Dept Biostat, Birmingham, AL 35294 USA
[8] Univ Calif Los Angeles, Sch Med, Dept Pathol, Los Angeles, CA 90024 USA
[9] Univ Calif Los Angeles, Sch Med, Dept Lab Med, Los Angeles, CA USA
[10] Canc Inst Gustave Roussy, Villejuif, France
[11] Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USA
[12] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[13] Univ Michigan, Dept Dermatol, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[14] Univ Pittsburgh, Sch Med, Dept Med, Div Oncol, Pittsburgh, PA 15213 USA
[15] Calif Pacific Med Ctr & Res Inst, Dept Surg, San Francisco, CA USA
[16] Univ Louisville, Dept Surg, Louisville, KY 40292 USA
[17] Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
[18] John Wayne Canc Inst, Santa Monica, CA USA
[19] Univ S Florida, H Lee Moffitt Canc Ctr, Div Cutaneous Oncol, Tampa, FL 33682 USA
关键词
LYMPH-NODE BIOPSY; PRIMARY CUTANEOUS MELANOMA; AMERICAN JOINT COMMITTEE; MULTIFACTORIAL ANALYSIS; PEDIATRIC MELANOMA; UNITED-STATES; MELANOCYTIC TUMORS; ADULT MELANOMA; SINGLE-CENTER; SURVIVAL;
D O I
10.1245/s10434-013-3100-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We postulated that the worse prognosis of melanoma with advancing age reflected more aggressive tumor biology and that in younger patients the prognosis would be more favorable. The expanded AJCC melanoma staging database contained 11,088 patients with complete data for analysis, including mitotic rate. With increasing age by decade, primary melanomas were thicker, exhibited higher mitotic rates, and were more likely to be ulcerated. In a multivariate analysis of patients with localized melanoma, thickness and ulceration were highly significant predictors of outcome at all decades of life (except for patients younger than 20 years). Mitotic rate was significantly predictive in all age groups except patients < 20 and > 80 years. For patients with stage III melanoma, there were four independent variables associated with patient survival: number of nodal metastases, patient age, ulceration, and mitotic rate. Patients younger than 20 years of age had primary tumors with slightly more aggressive features, a higher incidence of sentinel lymph node metastasis, but, paradoxically, more favorable survival than all other age groups. In contrast, patients > 70 years old had primary melanomas with the most aggressive prognostic features, were more likely to be head and neck primaries, and were associated with a higher mortality rate than the other age groups. Surprisingly, however, these patients had a lower rate of sentinel lymph node metastasis per T stage. Among patients between the two age extremes, clinicopathologic features and survival tended to be more homogeneous. Melanomas in patients at the extremes of age have a distinct natural history.
引用
收藏
页码:3961 / 3968
页数:8
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