[Late-onset neutropenia following rituximab therapy as a treatment of diffuse large B-cell lymphoma: a single institution study].

Minki Kim, Jin Kyung Lee, Young Jun Hong, Seok-Il Hong, Hye Jin Kang, Yoon Hwan Chang
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引用次数: 1

Abstract

Background: Late-onset neutropenia (LON) following rituximab therapy has been reported in recent years. However, its incidence has not been reported in Korea. The aim of this study is to investigate the incidence of LON after rituximab therapy in Korean patients with diffuse large B-cell lymphoma (DLBCL).

Methods: Ninety-eight cases of DLBCL treated with rituximab between 2004 and 2008 were evaluated. We identified LON as defined by the neutrophil count of <1.5 × 10(9)/L without apparent cause after the recovery of neutrophil count following rituximab therapy. Bone marrow aspiration and biopsy specimens at the time of neutropenia were available for retrospective review in only 5 of the patients.

Results: LON was observed in 15 (15.3%) of the 98 patients. In the bone marrow specimens of the 5 patients, promyelocytes were relatively increased and the maturation index of the granulopoiesis was 2:1-3:1, which reflects maturation arrest.

Conclusions: The incidence of LON following rituximab therapy was 15.3% in Korean patients with DLBCL. Although there are several hypotheses about the causative mechanisms of LON, we suggest that maturation arrest at the promyelocyte stage of granulopoiesis may be one of the mechanisms involved in the development of LON.

[利妥昔单抗治疗弥漫性大b细胞淋巴瘤后迟发性中性粒细胞减少:一项单机构研究]。
背景:近年来已有利妥昔单抗治疗后迟发性中性粒细胞减少症(LON)的报道。但是,在国内还没有报道其发病率。本研究的目的是调查韩国弥漫性大b细胞淋巴瘤(DLBCL)患者利妥昔单抗治疗后LON的发生率。方法:回顾性分析2004 ~ 2008年利妥昔单抗治疗的98例DLBCL患者。结果:98例患者中有15例(15.3%)出现LON。5例患者骨髓标本中早幼粒细胞相对增多,粒细胞生成成熟指数为2:1-3:1,反映成熟阻滞。结论:韩国DLBCL患者利妥昔单抗治疗后LON的发生率为15.3%。尽管关于LON的病因机制有几种假设,但我们认为在粒细胞形成的早幼粒细胞阶段成熟停滞可能是LON发展的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Korean Journal of Laboratory Medicine
Korean Journal of Laboratory Medicine 医学-医学实验技术
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