Department of Surgery, University of Washington, Seattle2Division of Pediatric General and Thoracic Surgery, Seattle Children's Hospital, Seattle, Washington.
Department of Otolaryngology-Head and Neck Surgery, University of Washington, Seattle.
JAMA Otolaryngol Head Neck Surg. 2017 Jan 1;143(1):34-40. doi: 10.1001/jamaoto.2016.2630.
Melanoma in children is rare, accounting for approximately 2% of all pediatric malignant neoplasms. However, for the past 30 years, the incidence of melanoma in those younger than 20 years has been increasing. Location of the primary tumor has been shown to be an important prognostic factor, with melanomas of the scalp and neck conferring a worse prognosis than those originating at other sites.
To examine the survival, demographic, tumor, and treatment characteristics of pediatric head and neck melanoma.
DESIGN, SETTING, AND PARTICIPANTS: We performed a retrospective cohort study using information from the National Cancer Data Base from January 1, 1998, to December 31, 2012, on pediatric (≤18 years) and adult (>18 years) patients with head and neck melanoma. Data analysis was conducted from August 1, 2015, to June 30, 2016.
Pediatric age (≤18 years) at diagnosis of head and neck melanoma.
Survival differences were estimated using a Cox proportional hazards regression model. Surgical outcomes, including nodal sampling and margin status, were estimated with generalized linear models comparing pediatric and adult patients. Patient demographic, tumor, and treatment characteristics were estimated using t tests and χ2 tests between pediatric and adult patients with head and neck melanoma for continuous and categorical data, respectively.
Of the 84 744 patients with head and neck melanoma, 657 (0.8%) were 18 years or younger (mean [SD] age, 13.5 [4.7] years; 285 female and 372 male; 610 white). Pediatric and adult patients had similar demographics but different histologic subtypes (risk difference of pediatric vs adult patients: melanoma, not otherwise specified, 8.5% [95% CI, 4.7%-12.3%]; superficial spreading, 4.2% [95% CI, 0.89%-7.4%]; and lentigo maligna, -13.4% [95% CI, -14.1% to 12.6%]). Pediatric patients had tumors of similar mean depth to those in adult patients (pediatric, 1.54 mm; adult; 1.39 mm; absolute difference, 0.15 mm; [95% CI, -0.32 to 0.008]) and more frequent nodal metastases than did adult patients (risk difference of pediatric vs adult patients for stage T2, 23.9% [95% CI, 14.1%-33.6%]). Five-year survival among pediatric patients was higher for those with stage 1, 2, or 3 disease (absolute difference of pediatric vs adult patients: stage 1, 18% [95% CI, 9.7%-26.3%]; stage 2, 36% [95% CI, 25.3%-46.7%]; stage 3, 39% [95% CI, 26.8%-51.2%]; and stage 4, 2% [95% CI, -8.2% to 12.2%]).
Although pediatric patients with head and neck melanoma present with similar tumor depth and more frequent nodal metastases than do adult patients, younger patients have higher overall survival.
儿童黑色素瘤较为罕见,约占所有儿科恶性肿瘤的 2%。然而,在过去的 30 年中,20 岁以下儿童的黑色素瘤发病率一直在增加。肿瘤原发部位已被证明是一个重要的预后因素,头皮和颈部的黑色素瘤比其他部位的黑色素瘤预后更差。
研究儿童头颈部黑色素瘤的生存、人口统计学、肿瘤和治疗特征。
设计、地点和参与者:我们使用国家癌症数据库(National Cancer Data Base)从 1998 年 1 月 1 日至 2012 年 12 月 31 日的数据,对 18 岁及以下(≤18 岁)和 18 岁以上(>18 岁)的儿童和成人头颈部黑色素瘤患者进行了回顾性队列研究。数据分析于 2015 年 8 月 1 日至 2016 年 6 月 30 日进行。
诊断为头颈部黑色素瘤的儿童年龄(≤18 岁)。
采用 Cox 比例风险回归模型估计生存差异。通过广义线性模型比较儿科和成年患者,评估手术结果,包括淋巴结取样和边缘状态。使用 t 检验和χ2检验,分别对儿科和成年头颈部黑色素瘤患者的连续和分类数据进行比较,评估患者的人口统计学、肿瘤和治疗特征。
在 84744 例头颈部黑色素瘤患者中,有 657 例(0.8%)为 18 岁或以下(平均[标准差]年龄为 13.5[4.7]岁;女性 285 例,男性 372 例;610 例为白人)。儿科和成年患者的人口统计学特征相似,但组织学类型不同(儿科患者与成年患者相比:黑色素瘤,未特指,8.5%[95%CI,4.7%-12.3%];蔓延性黑色素瘤,4.2%[95%CI,0.89%-7.4%];和恶性雀斑样痣,-13.4%[95%CI,-14.1%至 12.6%])。儿科患者肿瘤的平均深度与成年患者相似(儿科患者 1.54 毫米;成年患者 1.39 毫米;绝对差异 0.15 毫米[95%CI,-0.32 至 0.008]),并且比成年患者更频繁发生淋巴结转移(儿科患者与成年患者相比,T2 期肿瘤的风险差异为 23.9%[95%CI,14.1%-33.6%])。儿科患者的 5 年生存率对于 I 期、II 期或 III 期疾病患者更高(儿科患者与成年患者相比的绝对差异:I 期,18%[95%CI,9.7%-26.3%];II 期,36%[95%CI,25.3%-46.7%];III 期,39%[95%CI,26.8%-51.2%];IV 期,2%[95%CI,-8.2%至 12.2%])。
尽管儿科头颈部黑色素瘤患者的肿瘤深度与成年患者相似,并且更频繁发生淋巴结转移,但年轻患者的总体生存率更高。