Department of Epidemiology, EpiFocus ltd, E11 2RJ London, United Kingdom.
Acta Derm Venereol. 2020 Jan 7;100(1):adv00013. doi: 10.2340/00015555-3367.
Most patients with mycosis fungoides are diagnosed with early-stage disease. However, prevalence of early-stage disease is unknown, and evidence of its burden is scarce. The aim of this study is to estimate the prevalence of early-stage mycosis fungoides, how long patients live with early-stage disease and to characterise these patients. Data were obtained from 4 key publications and from US cancer registries (Surveillance, Epidemiology and End Results Program; SEER). The derived incidence of early-stage mycosis fungoides was 0.26/100,000 (UK), 0.29/100,000 (US) and 0.38/100,000 (US-SEER) and the prevalence was 4.8/100,000 (UK), 5.2/100,000 (US) and 6.6/100,000 (US-SEER). Early-stage disease may last for 18 years. From SEER registries, 3,132 were diagnosed at early stage (mostly stage IA). Median age at diagnosis was 58 years. Compared with stage IA, the relative risk of death was 1.3 for stage IB and 3.5 for stage IIA. We confirm the rarity of early-stage mycosis fungoides, a differential prognosis and the potential for elevated burden of disease.
大多数蕈样肉芽肿患者被诊断为早期疾病。然而,早期疾病的流行情况尚不清楚,其负担的证据也很少。本研究旨在估计早期蕈样肉芽肿的流行率,患者患有早期疾病的时间长短,并对这些患者进行特征描述。数据来自 4 项主要出版物和美国癌症登记处(监测、流行病学和最终结果计划;SEER)。早期蕈样肉芽肿的推导发病率为 0.26/100,000(英国)、0.29/100,000(美国)和 0.38/100,000(美国-SEER),患病率为 4.8/100,000(英国)、5.2/100,000(美国)和 6.6/100,000(美国-SEER)。早期疾病可能持续 18 年。从 SEER 登记处,3132 例患者被诊断为早期(主要为 IA 期)。诊断时的中位年龄为 58 岁。与 IA 期相比,IB 期的死亡相对风险为 1.3,IIA 期为 3.5。我们证实了早期蕈样肉芽肿的罕见性、不同的预后和疾病负担增加的可能性。