Agner Kevin E, Larkins Michael C
The Ohio State University College of Medicine, 370 W. 9 Avenue, Columbus, OH 43210 USA.
East Carolina University Brody School of Medicine, 600 Moye Blvd, Greenville, NC 27834 USA.
Indian J Surg Oncol. 2024 Dec;15(4):809-815. doi: 10.1007/s13193-024-02002-z. Epub 2024 Jun 26.
Adamantinoma (AD) is a rare bone cancer accounting for less than 0.1-0.5% of all primary bone tumors. No consensus guidelines exist for the treatment of this disease and long-term (twenty-year) survival has yet to be explored. The Surveillance, Epidemiology, and End Results (SEER) Program was queried for patients with a diagnosis of primary AD (ICD-O-3 code 9261/3). Demographic and treatment variables were analyzed via Fisher's Exact Test and 20-year overall survival (20y OS) was assessed via log-rank analysis. Seventy-four patients with AD were identified; median age was 20-24 years. Multivariate analysis demonstrated that patients < 25 years of age at diagnosis with AD had increased 20y OS compared to those > 24 years (HR = 0.28; p = 0.028), while no other variables influenced survival. Subanalysis demonstrated patients > 40 years saw decreased survival (46% [11%, 81%]) compared to those ≤ 40 years (96% [89%, 104%]; p = 0.005). Patients ≤ 40 years of age at diagnosis were more likely to have local disease (78% of all 49 local cases) and less likely to have distant disease (0% of two cases) compared to patients > 40 years (p = 0.017). Stratifying by surgical procedure, no difference in 20y OS was appreciated (p = 0.12). Younger age at diagnosis provides mortality benefit and increased proportion of localized disease for those diagnosed with AD. No other demographic or treatment variables were found to influence 20y OS. Population-based analysis of AD is limited both by disease rarity and incomplete coding within SEER.
成釉细胞瘤(AD)是一种罕见的骨癌,占所有原发性骨肿瘤的比例不到0.1 - 0.5%。目前对于该疾病的治疗尚无共识性指南,其长期(20年)生存率也有待探索。我们向监测、流行病学和最终结果(SEER)项目查询了诊断为原发性AD(国际疾病分类肿瘤学第三版代码9261/3)的患者。通过Fisher精确检验分析人口统计学和治疗变量,并通过对数秩分析评估20年总生存率(20y OS)。共识别出74例AD患者;中位年龄为20 - 24岁。多变量分析表明,诊断为AD时年龄<25岁的患者与年龄>24岁的患者相比,20y OS有所增加(风险比=0.28;p = 0.028),而其他变量均未影响生存率。亚组分析表明,年龄>40岁的患者与年龄≤40岁的患者相比,生存率降低(46%[11%,81%])(96%[89%,104%];p = 0.005)。与年龄>40岁的患者相比,诊断时年龄≤40岁的患者更易出现局部疾病(49例局部病例中的78%),且远处疾病的可能性更小(2例中的0%)(p = 0.017)。按手术方式分层,未发现20y OS有差异(p = 0.12)。诊断时年龄较小对诊断为AD的患者有生存获益,并增加局部疾病的比例。未发现其他人口统计学或治疗变量影响20y OS。基于人群的AD分析受到疾病罕见性和SEER内编码不完整的限制。