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套细胞淋巴瘤的流行病学:法国的一项基于人群的研究。

Mantle cell lymphoma epidemiology: a population-based study in France.

机构信息

Service d'Évaluation Médicale et d'Épidémiologie, Centre Hospitalier Universitaire de Nantes, Nantes, France.

出版信息

Ann Hematol. 2014 Aug;93(8):1327-33. doi: 10.1007/s00277-014-2049-5. Epub 2014 Apr 25.

DOI:10.1007/s00277-014-2049-5
PMID:24763513
Abstract

Only limited population-based data are available on mantle cell lymphoma (MCL), a relatively rare and aggressive mature B cell non-Hodgkin lymphoma (NHL) entity. We conducted an epidemiological study based on the three French registries devoted to haematological malignancies over the period 2002-2006. Main clinical features and management characteristics were collected. Incidence and survival rates were estimated, and independent prognostic factors were analysed. MCL was diagnosed in 135 patients between 2002 and 2006. Seventy-four percent of patients were men. Age-standardised incidence rate of MCL (per 100,000) was 1.1 in men and 0.26 in women. Median age at diagnosis was 72 years (range 30-92). Advanced-stage (III or IV) disease was diagnosed in 81.5 % of patients, and 55 % of them were identified as high risk according to MCL International Prognostic Index (MIPI). Median net survival time was 41 months (95 % confidence interval (CI), 38-62). Main independent prognostic factors were age at diagnosis, performance status and use of rituximab in first-line treatment. Median overall survival was 36 months (95 % CI, 27-40) for high MIPI and 60 months (95 % CI, 35-74) for low/intermediate MIPI patients (p = 0.02). This study confirms that MCL remains an aggressive NHL with a median overall survival less than 4 years and demonstrates that the use of rituximab has modified overall survival duration.

摘要

仅有有限的基于人群的资料可用于套细胞淋巴瘤(MCL),这是一种相对罕见且侵袭性强的成熟 B 细胞非霍奇金淋巴瘤(NHL)实体。我们基于 2002-2006 年期间致力于血液恶性肿瘤的三个法国登记处进行了一项流行病学研究。收集了主要的临床特征和治疗特征。估计了发病率和生存率,并分析了独立的预后因素。2002 年至 2006 年间诊断出 135 例 MCL 患者。74%的患者为男性。MCL 的年龄标准化发病率(每 10 万人)在男性中为 1.1,在女性中为 0.26。诊断时的中位年龄为 72 岁(范围 30-92)。81.5%的患者诊断为晚期(III 或 IV 期)疾病,其中 55%根据 MCL 国际预后指数(MIPI)被鉴定为高危。中位无进展生存时间为 41 个月(95%置信区间[CI],38-62)。主要的独立预后因素是诊断时的年龄,表现状态和在一线治疗中使用利妥昔单抗。高 MIPI 患者的中位总生存期为 36 个月(95%CI,27-40),低/中 MIPI 患者为 60 个月(95%CI,35-74)(p = 0.02)。这项研究证实,MCL 仍然是一种侵袭性 NHL,中位总生存期不到 4 年,并表明利妥昔单抗的使用已改变了总生存时间。

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