首页> 外文期刊>International Journal of Hematology >Multiple mucosa-associated lymphoid tissue organs involving marginal zone B cell lymphoma: organ-specific relationships and the prognostic factors. Consortium for improving survival of lymphoma study
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Multiple mucosa-associated lymphoid tissue organs involving marginal zone B cell lymphoma: organ-specific relationships and the prognostic factors. Consortium for improving survival of lymphoma study

机译:涉及边缘区B细胞淋巴瘤的多个与粘膜相关的淋巴组织器官:器官特异性关系和预后因素。改善淋巴瘤生存研究的联盟

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According to a previous review, multiple mucosa-associated lymphoid tissue (MALT)-organs involving marginal zone B cell lymphomas (MZLs) are present in 10–30% of patients. However, the clinical features and specific relationships among involved organs are yet to be clearly identified. In this study, we conducted retrospective analyses of multiple MALT organs involving MZLs (MM-MZLs) to identify their clinical features, treatment, prognosis, and specific relationships among involved organs. For analysis, between June 1987 and June 2009, a total of 55 patients from 17 different institutions in Korea, all of whom were histologically diagnosed with MM-MZL, were included in this study. MM-MZL was defined as MZL involving more than 2 different MALT organs. Multiple involvements within one MALT organ (e.g. both side ocular lesions, multiple lung nodules, and multiple stomach lesions, etc.) were excluded from this study. The male/female ratio of the 55 patients was 41/14. The median age of our subjects was 59 years (range 30–82 years). MM-MZL without lymph node (LN) was detected only in 9 patients (36.2%). Bone marrow (BM) involvement was observed in 17 patients (30.9%). The most common site of involvement was the gastrointestinal (GI) tract (25 patients, 45.5%) followed by the lung (40%), Waldeyer’s ring (WR) (27.3%), and ocular area (25.5%). Ocular MZLs were commonly accompanied with WR- or lung-MZLs. GI-MZLs were WR or GI-MZLs. Lung-MZLs were frequently observed with ocular and GI-MZLs. WR-MZLs were ocular or GI-MZLs. A total of 53 patients were treated, and 2 on watchful wait. As much as 48 patients received chemotherapy-based treatment. Among them, CR or PR was achieved in 38 patients (79.2%, 95% CI 67–91%). Median time to progression (TTP) was 2.3 years (95% CI 1.4–3.2 years). Cause-specific overall survival (OS) did not reach the median value. The 5-year OS rate was 84.9%. MM-MZLs tend to be an indolent disease, characterized by prolonged survival with frequent relapses. The majority of cases could be controlled effectively via chemotherapy-based treatment, and prolonged survival was achieved in those patients. The GI, lung, WR, and ocular area were commonly presented with other MALT site MZLs, and an organ-specific relationship appears to be relevant to MM-MZLs.
机译:根据先前的评论,10-30%的患者中存在涉及边缘B区细胞淋巴瘤(MZL)的多个黏膜相关淋巴样组织(MALT)-器官。但是,尚不清楚相关器官之间的临床特征和特定关系。在这项研究中,我们对涉及MZL(MM-MZL)的多个MALT器官进行了回顾性分析,以确定它们的临床特征,治疗,预后以及所涉器官之间的特定关系。为了进行分析,从1987年6月到2009年6月,来自韩国17个不同机构的55名患者经组织学诊断均为MM-MZL,纳入本研究。 MM-MZL被定义为涉及2个以上MALT器官的MZL。该研究排除了一个MALT器官内的多处受累(例如两侧眼部病变,多个肺结节和多个胃部病变等)。 55名患者中的男女比例为41/14。我们受试者的中位年龄为59岁(30-82岁)。仅9例(36.2%)检出无淋巴结(LN)的MM-MZL。在17名患者中观察到了骨髓(BM)受累(30.9%)。最常见的受累部位是胃肠道(25例,占45.5%),其次是肺(40%),瓦尔德环(WR)(27.3%)和眼部区域(25.5%)。眼部MZL通常伴有WR-或肺部MZL。 GI-MZL是WR或GI-MZL。肺部MZL经常与眼部和胃肠道MZL一起观察到。 WR-MZL是眼用或GI-MZL。总共治疗了53例患者,其中2例经过了等待观察。多达48位患者接受了基于化学疗法的治疗。其中,有38例患者获得CR或PR(79.2%,95%CI 67-91%)。中位进展时间(TTP)为2.3年(95%CI为1.4-3.2年)。特定原因的整体生存率(OS)未达到中值。 5年OS率为84.9%。 MM-MZLs往往是一种惰性疾病,其特点是生存期延长且经常复发。大多数病例可以通过基于化学疗法的治疗得到有效控制,并且这些患者的生存期得以延长。胃肠道,肺,WR和眼部区域通常与其他MALT部位MZL一起出现,并且器官特异性关系似乎与MM-MZL有关。

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