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美国利妥昔单抗治疗时代前后弥漫性大 B 细胞淋巴瘤的生存情况。

Survival in advanced diffuse large B-cell lymphoma in pre- and post-rituximab Eras in the United States.

机构信息

Cancer Center and Blood Institute, St Joseph Regional Medical Center, Lewiston, ID, U.S.A.

Department of Statistical Sciences, University of Idaho, Moscow, ID, U.S.A.

出版信息

Anticancer Res. 2014 Sep;34(9):5117-20.

Abstract

BACKGROUND

Rituximab was approved by the United States Food and Drug Administration (FDA) as a first-line agent for treatment of advanced diffuse large B-cell lymphoma (DLBCL) in February 2006. We conducted this population-based study to determine if the results from the clinical trials have translated into survival benefit in the general population.

PATIENTS AND METHODS

We selected patients with advanced diffuse large B-cell lymphoma from the Surveillance, Epidemiology, and End RESULTS (SEER) 18 database, and calculated relative survival rates for patients diagnosed from 2002-2005 (pre-rituximab) and 2006-2009 (post-rituximab). We used the Z-test in the SEER*Stat to compare relative survival rates of patients categorized by race (White, Black, or Others), gender (male, female), and age groups (<60, 60+ years).

RESULTS

One-year relative survival in Whites and Others improved significantly in the post-rituximab era compared to the pre-rituximab era (64.80±0.6% vs. 61.3±0.6%; p=0.0002 and 64.5±1.9% vs. 54.9±2.2%; p=0.0011, respectively). The 3-year relative survival improved significantly in Whites and Others in the post-rituximab era compared to the pre-rituximab era (53.7±0.7% vs. 50.3±0.7%; p=0.0001 and 52.0±2.3% vs. 40.8±2.3%; p=0.0002, respectively). However, no significant improvements were observed in 1-year and 3-year relative survival in Blacks, and in young males during the post-rituximab era compared to the pre-rituximab era.

CONCLUSION

The relative survival rates among young males and 'Black' patients with advanced diffuse large B-cell lymphoma have not improved during the post-rituximab era.

摘要

背景

利妥昔单抗于 2006 年 2 月被美国食品和药物管理局(FDA)批准为治疗晚期弥漫性大 B 细胞淋巴瘤(DLBCL)的一线药物。我们进行了这项基于人群的研究,以确定临床试验的结果是否转化为普通人群的生存获益。

患者和方法

我们从监测、流行病学和最终结果(SEER)18 数据库中选择了晚期弥漫性大 B 细胞淋巴瘤患者,并计算了 2002-2005 年(利妥昔单抗前)和 2006-2009 年(利妥昔单抗后)诊断患者的相对生存率。我们使用 SEER*Stat 中的 Z 检验比较了按种族(白种人、黑种人或其他人)、性别(男、女)和年龄组(<60 岁、60 岁以上)分类的患者的相对生存率。

结果

白人和其他人的 1 年相对生存率在利妥昔单抗后时代明显高于利妥昔单抗前时代(64.80±0.6%比 61.3±0.6%;p=0.0002 和 64.5±1.9%比 54.9±2.2%;p=0.0011)。白人和其他人的 3 年相对生存率在利妥昔单抗后时代明显高于利妥昔单抗前时代(53.7±0.7%比 50.3±0.7%;p=0.0001 和 52.0±2.3%比 40.8±2.3%;p=0.0002)。然而,在利妥昔单抗后时代,年轻男性和黑人的 1 年和 3 年相对生存率并没有显著改善。

结论

在利妥昔单抗后时代,年轻男性和晚期弥漫性大 B 细胞淋巴瘤“黑人”患者的相对生存率没有提高。

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