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骨恶性巨细胞瘤的流行病学:监测、流行病学和最终结果计划(1975 - 2004年)数据分析

The epidemiology of malignant giant cell tumors of bone: an analysis of data from the Surveillance, Epidemiology and End Results Program (1975-2004).

作者信息

Beebe-Dimmer Jennifer L, Cetin Karynsa, Fryzek Jon P, Schuetze Scott M, Schwartz Kendra

机构信息

Karmanos Cancer Institute and Wayne State University Department of Internal Medicine, Detroit, MI;

出版信息

Rare Tumors. 2009 Dec 28;1(2):e52. doi: 10.4081/rt.2009.e52.

Abstract

Malignant giant cell tumor (GCT) of bone is a rare tumor with debilitating consequences. Patients with GCT of bone typically present with mechanical difficulty and pain as a result of bone destruction and are at an increased risk for fracture. Because of its unusual occurrence, little is known about the epidemiology of malignant GCT of bone. This report offers the first reliable population-based estimates of incidence, patient demographics, treatment course and survival for malignancy in GCT of bone in the United States. Using data from the National Cancer Institute's Surveillance, Epidemiology and End Results (SEER) program, we estimated the overall incidence and determinants of survival among patients diagnosed with malignant GCT of bone from 1975-2004. Cox proportional hazards regression was used to evaluate demographic and clinical determinants of survival among malignant GCT cases. Based on analyses of 117 malignant GCT cases, the estimated annual incidence in the United States was 1.6 per 10,000,000 persons per year. Incidence was highest among adults aged 20 to 44 years (2.4 per 10,000,000 per year) and most patients were diagnosed with localized (31.6%) or regional (29.9%) disease compared to distant disease (16.2%). Approximately 85% of patients survived at least 5 years, with survival poorest among older patients and those with evidence of distant metastases at time of diagnosis. The current study represents the largest systematic investigation examining the occurrence and distribution of malignancy in GCT of bone in the general U.S. population. We confirm its rare occurrence and suggest that age and stage at diagnosis are strongly associated with long-term survival.

摘要

骨恶性巨细胞瘤(GCT)是一种罕见肿瘤,会产生严重后果。骨GCT患者通常因骨质破坏而出现机械性困难和疼痛,骨折风险也会增加。由于其发病情况不常见,人们对骨恶性GCT的流行病学知之甚少。本报告首次提供了基于可靠人群的美国骨GCT恶性肿瘤发病率、患者人口统计学特征、治疗过程和生存率的估计数据。利用美国国立癌症研究所监测、流行病学和最终结果(SEER)项目的数据,我们估计了1975年至2004年期间被诊断为骨恶性GCT患者的总体发病率和生存决定因素。采用Cox比例风险回归来评估恶性GCT病例生存的人口统计学和临床决定因素。基于对117例恶性GCT病例的分析,美国每年的估计发病率为每1000万人中有1.6例。发病率在20至44岁的成年人中最高(每年每1000万人中有2.4例),与远处疾病(16.2%)相比,大多数患者被诊断为局限性(31.6%)或区域性(29.9%)疾病。约85%的患者至少存活了5年,老年患者以及诊断时已有远处转移证据的患者生存率最差。本研究是对美国普通人群骨GCT恶性肿瘤的发生和分布进行的最大规模系统调查。我们证实了其罕见性,并表明诊断时的年龄和分期与长期生存密切相关。

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