在肾功能受损的 CLL 患者中,β-2-微球蛋白对首次治疗时间的预后价值降低。

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2024-08-21 DOI:10.1080/10428194.2024.2394583
Jan-Paul Bohn, Valentina Stolzlechner, Georg Göbel, Markus Pirklbauer, Dominik Wolf, Normann Steiner
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引用次数: 0

摘要

慢性淋巴细胞白血病(CLL)是成人中最常见的白血病,其临床病程具有高度异质性。CLL-IPI 和 OCLL-1 评分是预测首次治疗时间的最佳验证工具之一。在这两个模型中,β-2-微球蛋白血浆水平(B2M)的升高是一个独立的预后因素。然而,慢性肾脏病(CKD)患者的 B2M 通常本身就会升高,而且这两个模型都没有对 CKD 进行调整。我们分析了 2000 年至 2022 年间 297 例未经治疗的 CLL 患者的临床结果。B2M在CKD患者中更常升高,在阈值> 2.5 mg/L时失去预后意义。CLL-IPI和OCLL-1都无法帮助对CKD患者进行预后分类。22.2%的 CKD 患者因 B2M 升高而被分配到较高的 CLL-IPI 风险组。我们的研究结果表明,这两种模型都高估了疾病进展的风险,因此需要对 CKD 患者谨慎解读。
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Reduced prognostic value of beta-2-microglobulin for time to first treatment in CLL patients with compromised kidney function.

Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults and characterized by a highly heterogeneous clinical course. The CLL-IPI and the OCLL-1 scores are among the best validated tools to predict time-to-first-treatment. In both models, elevated beta-2-microglobulin plasma level (B2M) is an independent prognostic factor. Yet, B2M is commonly increased in patients with chronic kidney disease (CKD) per se and both models were not adjusted for CKD. We analyzed the clinical outcomes of 297 treatment-naive CLL patients between 2000 and 2022. B2M was more frequently elevated in CKD patients and lost prognostic significance at the threshold > 2.5 mg/L. Both CLL-IPI and OCLL-1 failed to facilitate prognostic segregation in CKD patients. 22.2% of CKD patients were assigned to a higher CLL-IPI risk group due to elevated B2M. Our results suggest that both models overestimate the risk for disease progression and need to be interpreted with caution in CKD patients.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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