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

机译: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)的数据分析

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摘要

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.
机译:骨骼的恶性巨细胞瘤(GCT)是一种罕见的肿瘤,具有使人衰弱的后果。患有骨GCT的患者通常由于骨破坏而出现机械困难和疼痛,骨折风险增加。由于其异常发生,因此对骨恶性GCT的流行病学知之甚少。该报告提供了美国第一个可靠的基于人群的骨GCT发病率,患者人口统计学,治疗过程和恶性生存率的估计值。利用美国国家癌症研究所监视,流行病学和最终结果(SEER)计划的数据,我们估算了1975-2004年诊断为骨GCT的患者的总发病率和生存率。 Cox比例风险回归用于评估恶性GCT病例中生存的人口统计学和临床​​决定因素。根据对117例恶性GCT病例的分析,在美国,估计的年发病率为每10,000,000人每年1.6。在20至44岁的成年人中发病率最高(每年每10,000,000个中有2.4个),与远处疾病(16.2%)相比,大多数患者被诊断出患有局部疾病(31.6%)或区域性疾病(29.9%)。大约85%的患者至少活了5年,在老年患者和诊断时有远处转移证据的患者中,存活率最差。当前的研究代表了一项最大的系统研究,旨在检查美国普通人群骨GCT中恶性肿瘤的发生和分布。我们确认其罕见的发生,并建议诊断时的年龄和阶段与长期生存密切相关。

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