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弥漫性大 B 细胞淋巴瘤患者的晚期复发:利妥昔单抗对其发生率和结局的影响。

Late relapse in patients with diffuse large B-cell lymphoma: impact of rituximab on their incidence and outcome.

机构信息

Oncology Institute of Southern Switzerland (IOSI), Bellinzona, Switzerland.

Division of Haematology, Department of Internal Medicine, Ospedale degli Infermi, Biella, Italy.

出版信息

Br J Haematol. 2019 Nov;187(4):478-487. doi: 10.1111/bjh.16106. Epub 2019 Aug 5.

DOI:10.1111/bjh.16106
PMID:31385291
Abstract

Diffuse large B-cell lymphoma (DLBCL) constitutes 25-35% of all non-Hodgkin lymphomas in Western countries. Approximately two thirds of the patients can be cured with standard immuno-chemotherapy. Most relapses occur within 1-2 years from diagnosis, however, the occurrence of relapses after 5 years or more has been described. We aimed at defining the incidence and clinical features of late relapses. Data of 1113 DLBCL patients were analysed. Among the 196 patients relapsing after a first complete remission, 36 (18% of relapses and 3% of all DLBCLs) experienced a recurrence more than 5 years from diagnosis. Late relapsing patients, in comparison with those relapsing earlier, showed a more favourable risk profile at presentation: normal lactate dehydrogenase levels (P = 0·002), early Ann Arbor stage (P = 0·006) and low International Prognostic Index (P = 0·003). The risk of late relapse was lowered by the introduction of rituximab as part of the front-line treatment (P < 0·001). Cause-specific survival (CSS) from the time of relapse was significantly better for late relapsing patients compared to those relapsing early: 5-year CSS rates were 53% and 31%, respectively (P = 0·033). A trend toward a better overall survival was also observed, with 5-year rates after relapse of 47% and 25%, respectively (P = 0·054).

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)构成西方国家所有非霍奇金淋巴瘤的 25-35%。大约三分之二的患者可以通过标准的免疫化学疗法治愈。大多数复发发生在诊断后 1-2 年内,但也有描述在 5 年或更长时间后发生复发的情况。我们旨在定义晚期复发的发生率和临床特征。分析了 1113 例 DLBCL 患者的数据。在首次完全缓解后复发的 196 例患者中,有 36 例(复发的 18%和所有 DLBCL 的 3%)在诊断后 5 年以上复发。与早期复发的患者相比,晚期复发的患者在发病时表现出更有利的风险特征:正常乳酸脱氢酶水平(P=0·002)、早期 Ann Arbor 分期(P=0·006)和低国际预后指数(P=0·003)。利妥昔单抗作为一线治疗的一部分的引入降低了晚期复发的风险(P<0·001)。从复发时起,晚期复发患者的无病生存率(CSS)明显优于早期复发患者:5 年 CSS 率分别为 53%和 31%(P=0·033)。观察到总生存率也有改善的趋势,复发后 5 年的生存率分别为 47%和 25%(P=0·054)。

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