[慢性b淋巴细胞白血病诊断时预后因素的重要性]。

Sbornik lekarsky Pub Date : 2002-01-01
E Cmunt, K Michalová, L Sindelárová, J Karban, Z Zemanová, S Kurková, J Brezinová, J Schwarz, Z Bosáková
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引用次数: 0

摘要

背景:b慢性淋巴细胞白血病(B-CLL)是西方国家最常见的成人白血病。任何常规使用的分期系统在诊断时都不能准确区分疾病的可能病程。因此,新的预后因素,这有助于评估患者的最佳治疗方案,被密集搜索。方法和结果:我们评估了154例诊断时患有B-CLL的患者,其中133例回顾性分为两组,一组为稳定型,另一组为进展型。我们比较了两组患者的一些预后因素(淋巴细胞绝对计数、c反应蛋白、乳酸脱氢酶、β -2微球蛋白、肿瘤坏死因子水平、免疫球蛋白水平、CD38、FMC7、表面免疫球蛋白的表达、骨髓浸润类型和细胞遗传学异常(12三体、del(13)(q14)、del(17)(p13)和del(11)(q23))。我们发现,随着疾病的进展,淋巴细胞绝对计数、β -2微球蛋白、肿瘤坏死因子、CD38、轻链lambda的表达、FMC7的表达和结节型骨髓浸润的频率降低。细胞遗传学异常与RAI等[27]分期系统的病程或分期相关性不显著,可能是由于评估的患者数量少,随访时间短。结论:b -慢性淋巴细胞白血病患者在诊断时的一些危险因素的常规评估有助于区分那些可能具有更大病程的疾病,并对设计适合风险的治疗策略具有指导意义。细胞遗传学异常和其他危险因素对预后的影响需要在更大的患者群体中进行更长的随访和反复评估。
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[Importance of prognostic factors in patients with chronic B-lymphocytic leukemia at the time of diagnosis].

Background: B-chronic lymphocytic leukemia (B-CLL) is the most common adult leukemia in the Western countries. Any routinely used staging system does not distinguish exactly the probable course of the disease at the time of diagnosis. Therefore the new prognostic factors, which help to assess the optimal therapeutic plan of patients, are searched intensively.

Methods and results: We evaluated 154 patients with the B-CLL at the time of diagnosis--133 of them were retrospectively divided into two groups--one with stable form and the other with progressive form of the disease. We compared these two groups of patients with some of the prognostic factors (absolute lymphocyte count, the level of C-reactive protein, lactatdehydrogenase, beta-2-microglobulin, tumour necrosis factor, the immunoglobulin levels, the expression of CD38, FMC7, surface immunoglobulins, the type of bone marrow infiltration, and the cytogenetic abnormalities (trisomy 12, del(13)(q14), del(17)(p13) a del(11)(q23)). We found higher absolute lymphocyte count, level of beta-2-mikroglobulin, tumour necrosis factor, expression of CD38, light chains lambda, lower expression of FMC7 and less frequent nodular type of bone marrow infiltration by the patients with progressive disease. The correlation of the cytogenetic abnormalities and the course of the disease or stage according to the RAI et al. [27] staging system were not significant may be due to the small number of evaluated patients and short period of follow up.

Conclusion: The routine evaluation of some risk factors in patients with B-chronic lymphocytic leukemia at the time of diagnosis helps to distinguish those with the probable more aggressive course of the disease and have the implication for the design of risk-adapted treatment strategies. The prognostic impact of the cytogenetic abnormalities and other risk factors has to be evaluated on larger group of patients during longer follow up period and repeated evaluations.

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