Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, USA.
Cancer. 2012 Aug 1;118(15):3786-92. doi: 10.1002/cncr.26700. Epub 2011 Dec 13.
Enteropathy-associated T-cell lymphoma (EATL) is a rare lymphoma subtype that is strongly associated with celiac disease (CD), an autoimmune disease triggered by the ingestion of gluten. Because CD rates are increasing in the United States, the authors sought to determine whether the incidence rates of EATL also are increasing.
The authors identified patients with primary, pathologically confirmed lymphoma in the Surveillance, Epidemiology, and End Results database registries from 1973 to 2008. To ensure capture of all cases of EATL, the following lymphoma subtypes, limited to the small bowel, were included: non-Hodgkin lymphoma not otherwise specified (NOS) T-cell, peripheral T-cell lymphoma NOS, and enteropathy type T-cell lymphoma, and their age-adjusted and sex-adjusted incidence rates were calculated over time. Survival was estimated using Kaplan-Meier curves.
In total, the authors identified 161 small bowel lymphomas that were diagnosed between 1973 and 2008. The overall age-adjusted and sex-adjusted annual incidence for all bowel lymphomas was 0.016 per 100,000 population, which increased over the study period from 0.006 to 0.024 per 100,000 population. These tumors were most common in men (age-adjusted incidence rate, 0.021 per 100,000) with the highest incidence rate in Hispanics (age-adjusted incidence rate, 0.033 per 100,000). The median overall survival was 7 months. There was no difference in survival by race/ethnicity (P = .09) or sex (P = .06).
The current results indicated a significant increase in the incidence of EATL in the United States, which may reflect the increasing seroprevalence of CD and better recognition of rare types of T-cell lymphomas. The incidence may continue to rise given the large ratio of undiagnosed-to-diagnosed individuals with CD in the United States.
肠病相关 T 细胞淋巴瘤(EATL)是一种罕见的淋巴瘤亚型,与乳糜泻(CD)密切相关,CD 是一种由摄入麸质引发的自身免疫性疾病。由于美国 CD 发病率不断上升,作者试图确定 EATL 的发病率是否也在上升。
作者从 1973 年至 2008 年的监测、流行病学和最终结果数据库登记册中确定了原发性、经病理证实的淋巴瘤患者。为确保捕获所有 EATL 病例,以下仅限于小肠的淋巴瘤亚型包括:非霍奇金淋巴瘤未另作说明(NOS)T 细胞、外周 T 细胞淋巴瘤 NOS 和肠病型 T 细胞淋巴瘤,并计算了随时间变化的年龄和性别调整发病率。使用 Kaplan-Meier 曲线估计生存情况。
作者总共确定了 161 例 1973 年至 2008 年期间诊断的小肠淋巴瘤。所有肠道淋巴瘤的年龄和性别调整年发病率为每 10 万人 0.016,研究期间从每 10 万人 0.006 增加到每 10 万人 0.024。这些肿瘤在男性中最常见(年龄调整发病率为每 10 万人 0.021),在西班牙裔中发病率最高(年龄调整发病率为每 10 万人 0.033)。中位总生存期为 7 个月。种族/族裔(P=0.09)或性别(P=0.06)对生存无影响。
目前的结果表明,美国 EATL 的发病率显著增加,这可能反映了 CD 的血清流行率不断上升以及对罕见 T 细胞淋巴瘤类型的更好认识。鉴于美国未确诊与确诊的 CD 个体之间的巨大比例,发病率可能会继续上升。