改良的分期系统和IPSS与改良IPSS在亚洲单中心Waldenström巨球蛋白血症队列中的比较表现的证据。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Jia Chen, Jian Li, Dao-Bin Zhou, Xin-Xin Cao
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引用次数: 0

摘要

Waldenström巨球蛋白血症(WM)是一种罕见的无法治愈的低级别b细胞淋巴瘤,表现出异质性的生存结果。我们在294例有症状的WM患者的单中心队列中,通过与现有模型的比较,评估了一种新的改进的WM分期系统(MSS-WM)的预后性能。MSS-WM表现出显著的分层能力(p p = 0.0002)。虽然MSS-WM与修订后的IPSS (rIPSS-WM)具有较高的一致性,但rIPSS-WM具有更好的预测准确性。然而,MSS-WM的简化结构增强了临床实用性,实现了快速的风险分层:低危组的5年生存率为89%,高危组为52%。这种实用的分期系统不需要复杂的计算,使其更适合常规临床实施,同时保持可比较的预后区分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence of the modified staging system and comparative performance of IPSS and revised IPSS in a Single-Center Asian cohort with Waldenström macroglobulinemia.

Waldenström macroglobulinemia (WM), a rare incurable low-grade B-cell lymphoma, exhibits heterogeneous survival outcomes. We evaluated the prognostic performance of a novel modified staging system of WM (MSS-WM) through comparison with existing models in a single-center cohort of 294 symptomatic WM patients. MSS-WM demonstrated significant stratification capacity (p < 0.0001), with 5-year overall survival rates of 89% (low-risk), 84% (low-intermediate), and 52% (intermediate/high-risk). All MSS-WM factors, including age, serum albumin, and LDH demonstrated independent prognostic impact. In addition, high beta-2 microglobulin level also showed negative prognostic impacts (p = 0.0002). While high concordance of MSS-WM and the revised IPSS (rIPSS-WM) was confirmed, the rIPSS-WM exhibited better predictive accuracy. However, MSS-WM's simplified structure enhances clinical utility, enabling rapid risk stratification: 89% 5-year survival in low-risk vs 52% in high-risk groups. This practical staging system requires no complex calculations, making it preferable for routine clinical implementation while maintaining comparable prognostic discrimination.

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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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