Hans-Based Cell of Origin Is Not of Prognostic Significance in Diffuse Large B-Cell Lymphoma Patients: A Retrospective Single-Center Study Conducted in 326 RCHOP-Treated Patients.

IF 2.8 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2026-01-01 Epub Date: 2025-12-18 DOI:10.1159/000549608
Marianthi Symeonidou, Stergios George Intzes, Konstantinos Zagoridis, Lazaros Karatisidis, Theodoros Mprotsis, Georgios Kanelis, Georgios Vrachiolias, Iliana Stamatiou, Zoe Bezirgiannidou, Bouse Malkots, Menelaos Papoutselis, Christoforos Roumpakis, Panagiotis Skendros, Panagiotis Tsikouras, Konstantinos Liapis, Ioannis Kotsianidis, Emmanouil Spanoudakis
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引用次数: 0

Abstract

Introduction: Diffuse large B-cell lymphoma (DLBCL) is a highly aggressive lymphoma with dismal outcome after disease progression. Individual risk assessment can stratify patients into different treatment strategies.

Methods: We retrospectively collected data from 326 DLBCL patients treated in a single center with RCHOP from 01/2000 to 06/2023. Immunohistochemistry by Han's algorithm was used to classify patients according to cell of origin (COO). The Kaplan-Meier estimator of survival and Cox regression analysis were used.

Results: Time to progression (TTP) and overall survival (OS) were not different according to COO. Univariate analysis reveals International Prognostic Index (IPI), b2-microglobulin ≥3.5 mg/L, bulky disease, and abnormal LDH, but not Han's defined COO, as the strongest predictors for progression. IPI score in multivariate analysis was the only prognostic factor for OS and together with high b2-microglobulin levels were independently prognostic factors for TTP. Accordingly, b2-microglobulin ≥3.5 mg/L was an independent prognostic factor for progression both in GC (hazard ratio [HR] 0.249 [(95% CI: 0.087-0.649), p = 0.004] and non-GC DLBCL patients (HR 0.380 [95% CI: 0.177-0.813], p = 0.011).

Conclusion: COO according to Hans index is not a significant prognostic factor for DLBCL patients, but b2-microglobulin ≥3.5 mg/L and IPI 2-5 in both GC and non-GC patients can predict individually a higher risk for progression.

题目:基于hans的细胞来源对DLBCL患者的预后没有意义;对326例RCHOP治疗患者进行回顾性单中心研究。
背景:弥漫性大b细胞淋巴瘤(DLBCL)是一种高度侵袭性淋巴瘤,疾病进展后预后不佳。个体风险评估可以对患者进行分层,采取不同的治疗策略。方法:我们回顾性收集了2000年1月至2023年6月在单一中心接受RCHOP治疗的326例DLBCL患者的资料。采用免疫组织化学Hans算法对患者按细胞来源(cell of origin, COO)进行分类。采用Kaplan-Meier生存估计和Cox回归分析。结果:两组患者的进展时间(Time to progression, TTP)和总生存期(overall survival, OS)无显著差异。单因素分析显示,国际预后指数(IPI), b2-微球蛋白≥3,5 mg/L,大体积疾病和异常LDH,但不是Han定义的COO,是进展的最强预测因素。多变量分析中IPI评分是OS的唯一预后因素,与高b2微球蛋白水平一起是TTP的独立预后因素。因此,b2-微球蛋白≥3.5 mg/L是胃癌(HR = 0,249 [(95% CI: 0,087-0,649), p=0,004]和非胃癌DLBCL患者[HR = 0,380 (95% CI: 0,177-0,813), p=0,011]进展的独立预后因素。结论:根据Hans指数计算的细胞来源并不是DLBCL患者的重要预后因素,但b2微球蛋白≥3,5 mg/L和IPI 2-5在GC和非GC患者中都可以单独预测更高的进展风险。
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
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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